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عمود فصل جديد لتقنية الكروماتوكرافيا السائلة عالي الاداء (HPLC) New column for high performance Liquid chromatography (HPLC)

اسم المؤلف: احمد مرزة حمزة
الموضوع العام: علوم الكيمياء
السنة: 2011
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: New stationary phases for high performance liquid chromatography has been prepared by the reaction of Bromophenol blue salt solution with Amberlite CG - 400 (ClP P) resin . The stability of the new attached functional group on the resin was studied against different solvents such as benzene, ethanol, acetonitrile, acetone, methanol, chloroform, and petroleum ether as well as NaOH and HCl solutions. The new prepared resin was found stable and no depletion of the Bromophenol blue moity from the resin was noticed with the above materials .The FTIR analysis has configured the attachment of Bromophenol on the resin as well as the physical appearance of the new resins.The new stationary phase has been packed into stainless steel column.The resin capacity of newly prepared resin has calculated. The resin capacity for the Amberlite - bromophenol blue salt was found to average 5.27 meq./g which is more than the Amberlite resin, 3.95 meq./g.The chromatographic performance of the packed column was characterized. The number of plate numbers N, height equivalent of a theoretical plates H, capacity factors Ḱ, selectivity factors α, and peaks asymmetry, and Resolution RRsR were measured by analyzing different analytes on the new columns using different mobile phase compositions and flow rates.These parameters were measured from analysis of some amino acids such as Histidine, Phenylalanine, Tryptophane, and Tyrosine. The analysis of amino acids using Amberlite - Bromophenol blue column has performed using %10 acetonitrile in water as mobile phase.The average value of plate numbers N was192.085. The plate heights H was averaged 0.089 cm , capacity factors Ḱ were ranged from 1.8 - 2.42. Separation factors α were ranged from 0.86 - 1.3 , and peak asymmetry value were range from 1.02 - 1.98 . Resolution Rs were ranged from 0.92 - 4.15 . R.S.D were ranged from(0.06 - 0.10)% , recovery were ranged from (95.84 - 96.88)% , The relative errors were ranged from ( - 3.12 - - 4.64) % . Calibration curves for all analyzed compound were linear from their detection limits to at least 50 ppm with correlation coefficient ranged from 0.9989 - 0.9996. The detection limits were ranged from 0.05 - 0.25 ppm at signal to noise ratio of three or more.

علاقة الهرمونات الجنسية بصورة الدهون المصلية والاجهاد التاكسدي في عقم الرجال

اسم المؤلف: ذو الفقار غانم محمد المحنه
اسم المشرف: سلمان علي احمد
الموضوع العام: علوم الكيمياء
السنة: 2010
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة نظرية لبعض معقدات المغنيز (III) الحاوي على ذرتي النيتروجين والاوكسجين Theoretical Studies for some Manganese (III) Complexes Containing Oxygen and Nitrogen Atoms

اسم المؤلف: احمد عبد الستار علي
اسم المشرف: مثنى عبد الجبار شنشل ایاد حمزة جاسم
الموضوع العام: علوم الكيمياء
السنة: 2009
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Reactive oxygen species (ROS) are small, highly reactive, oxygen containing molecules that are naturally generated in small amounts during the body’s metabolic reactions and can react with and damage complex cellular molecules such as fats, proteins, and DNA. Superoxide dismutase (SOD) represents an essential defense system against oxygen - derived free radicals, specifically superoxide (O2• - ). Superoxide can initiate a series of free radical reactions that yields other oxygen radicals, which together are thought to actas inflammatory mediators and induce cellular damage. The presence of natural superoxide dismutase (SOD), Catalase (CAT), and Glutathione Peroxidase (GPx) is to perform as defense systems against the cells damage which caused by superoxide compounds. These various enzymes allow to founding a widely area of treatment of many diseases.In our thesis, a series of ten Schiff - bases manganese (III) complexes which is previously prepared have been designed and build as SOD and CAT mimetics. The complexes along with the known Mn - Salen [(C1 : a known drug used as standard against superoxide anion (O2 - ) (SOD - mimetic activity) and hydrogen peroxide (H2O2) (CAT - mimetic activity)], have been characterized using the Gaussian 03 program (2003). The results show the following : 1. The manganese (III) ion in these complexes is surrounded by two nitrogen atoms of the Schiff - base, and two oxygen atoms and metal ion above the basal plane toward the anion (Cl - ).2. The behavior of building complexes is different in the oxidationreduction reactions.3. Some complexes which have mixed ligands (heteroligands), show to have better activities than that of the same ligands (homoligands).4. Some complexes get high mimetic enzyme activity in one reaction (SOD - mimetic or CAT - mimetic activities), but low mimetic enzyme activity in the other reactions.5. The activities of both C2 and C7 complexes are higher than that of C1 complex in both reaction types (SOD - mimetic and CAT - mimetic activities).6. The activities of (C4, C9, C10) complexes are higher mimetic enzyme than that of C1 complex as superoxide dismutase. 7. The activities of (C3, C5, C6, C8, C11) complexes are higher mimetic enzyme than that of C1 complex as Catalase.8. The calculation of geometrical shapes of building complexes were achieved by calculate the bond frequencies and force constant, the results indicate that all the building complexes have square pyramidal shape.

تحضير بعض قواعد شف كمثبطات لانزيم اليوريز ودراسة تاثيرها على بكتيريا المتقلبات Proteus M Preparation of some Schiff bases as Urease inhibitors and study their effect on Proteus mirabilis bacteria

اسم المؤلف: احمد حسين علي التميمي
الموضوع العام: علوم الكيمياء
السنة: 2010
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The current study involves preparation number of cysteine derivatives by the reaction of cysteine with different aromatic aldehydes forming the following Schiff bases : "2 - (4 - bromobenzylideneamino) - 3 - mercaptopropanoic acid, 2 - (4 - hydroxybenzylideneamino) - 3 - mercaptopropanoic acid, 2 - (4 - (dimethylamino)benzylideneamino) - 3 - mercaptopropanoic acid and 2 - (4 - chlorobenzylideneamino) - 3 - mercaptopropanoic acid".The new prepared derivatives were identified by using spectroscopy (FTIR) and measuring their melting points.The biological activities against Proteus mirabilis were estimated using well - diffusion method around the plate then the antibacterial activities were estimated.The effects of the prepared compounds on urease activity were studied. The results showed good effect in urease inhibition. All the prepared compounds showed competitive inhibition since the value Vmax was the same and Km increased.Finaly, Vmax, Ki, Km and i % values of the enzyme was calculated using line weaver Bruk equation.It is noticed from enzymatic and biological studies that Schiff bases compounds are strong inhibitors of the urease enzyme where the(2 - (4 - (dimethylamino)benzylideneamino) - - 3mercaptopropanoic acid ) inhibition force was (Ki=0.0043 M) which is the highest inhibition force comparing with the other prepared compounds.The percentage of inhibition (%i) was equal to (96.77%).

مقارنة التشخيص والتحاليل الحياتية لانزيم الفوسفاتيز القاعدي في الاكياس المائية المتكونة من جنس Echinococcus Granulosus ومصل دم الانسان

اسم المؤلف: مريم فضيل ناصر
اسم المشرف: سلمان علي احمد
الموضوع العام: علوم الكيمياء
السنة: 2009
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Hydatidosis, a zoonitic parasitic disease, is one of the most important economic and health problem in Iraq and many other countries in the Middle East. It is caused by Echinococcus Multilocularis and Echinococcus granulosus, the larval stage of which is localized in the liver, lungs and other visceral organs of intermediate hosts such as sheep, goats and cattle.Human are considered to be an accidental intermediate host, either by eating improperly disinfected vegetables or by close contact with dogs. The mature form lives in the ileum of candies as its definitive hosts, where it leads to an asymptomatic infection .Serology or immunodiagnostic tests are the most useful techniques for the detection of hydatid cysts in human patients.Objectives : One of the reasons why Echinococcus granulosus cysts are described as a public health problem is the lack of effective chemotherapy.Reviewing the literature bears in mind the possibility of an effectual and successful chemotherapeutic treatment in the early stages of cyst development, as indicated by many reported studies. Thus, the major problem in the management of Hydatid disease seems to be related to the lack of an efficient routine diagnostic test capable of identifying asymptomatic patients at early stages of the disease. Consequently, the need for a consistent diagnostic test, applicable for mass screening in hyperendemic regions, has become mandatory.Much attention has been focused on the multilocularis species which represent the major type affecting western countries. These cumulative efforts have recently evolved a commercially available and reliable immunodiagnostic test for the specific diagnosis of Alveolar ehinococcus. Unfortunately, the test fails to identify most of the patients suffering from cystic echinococcosis, caused by the closely related echinococcus granulosus.Hence, this will detract from the valuablity of the test in districts, where echinococcus granulosus is well known as the main endemic type, including Iraq, and necessitating the requirement for further studies with regard to echinococcus granulosus.The present study was conducted to estimate the kinetic parameters and biochemical characteristics of alkaline phosphatase in fertile and sterile cyst membranes from patients with hepatic cystic echinococcosis. The raised alkaline phosphatase serums of patients suffering cholestasis caused by gallstones were used as a representative alternate to Human liver - type alkaline phosphatase. Comparisons were aimed to reveal whether these two cyst membranes enzymes are different from each other and from the Human liver - type alkaline phosphatase.Subject and methods : In this study two samples were used, the cyst and human serum.Hydatid cysts were obtained from six hepatic cystic echinococcosis patients attending The Red Crescent Private Hospital, Baghdad, for surgical intervention from January 2007 through August 2008. Based on ultrasonographic examination, only two were identified as fertile, three were sterile and one patient with calcified cyst.Fasting venous blood samples were acquired from patients with professional diagnosis of gallstones, attending the above hospital for surgical treatment. Serum was separated, 5' - nucleotidase activity was measured to confirm that the raised alkaline phosphatase activity is mainly due to liver isoenzymeCollected serum samples were pooled and divided into aliquots, stored at - 2 C until further analysis.The present study was measurement of alkaline phosphatase activity in serum and cyst homogenate according to the method of kind and king.Kinetic studies will involve the affinity of these enzymes to their substrate, as well as the effect of other factors including hydrogen ion concentration (pH) and temperature. Heat inactivation and the effect of specific inhibitor, namely L - phenylalanine, are also to be examined on the activity of the three alkaline phosphatase enzymes.Results : 1.Different alkaline phosphatase activity were observed in fertile cysts while there was no alkaline phosphatase activity in hydatid cyst homogenated from sterile cysts and still not able to be detected even when larger volume of the hydatid cyst homogenated sample were used for the estimation and can be explained that by the presence or the absence of fresh protoscoleces in fertile or sterile hydatid cyst, respectively. Because of this statement it can be differentiate between the sterile & fertile cyst.By the results of the biochemical characterization of alkaline phosphatase, there were different Km values, optimum pH and optimum temperature for each hydatid cyst homogenated & human - liver type.The heat - sensitive specifically showed that the echinococcus granulosus alkaline phosphatase was more heat resistance than echinococcus multilocularis & liver - type enzyme.The respond of different human alkaline phosphatse isoenzymes to L - phenylalanine have been shown to varied from low sensitive (liver and bone) to highly sensitive (placental and intestinal). Thus, the wide range of IC50 observed herein, can be ascribed to the presence of isoenzymes other than liver type in the serum samples enrolled in this study. No inhibitory effect was observed on alkaline phosphatase from hydatid cyst homogenate.Conclusion : Considering present findings along with the following discussion, the following conclusions might be derived : Echinococcus granulosus Alkaline Phosphatase serve as a marker of cyst viability.The different characteristic of alkaline phosphatase from hydatid cyst membrane revealed that echinococcus granulosus Alkaline phosphatase is distinct from human isoenzymes more specifically from liver alkaline phosphatase isoenzyme.

دراسة امتزاز وامتصاص بعض الملوثات العضوية على ثنائي اوكسيد التتانيوم Sorption study of Some Organic Pollutants on Titanium Dioxide

اسم المؤلف: قيس محمد عبد الحسين
اسم المشرف: خلود عبد صالح السعدي
الموضوع العام: علوم الكيمياء
السنة: 2009
الموضوع الدقيق: الكيمياء الفيزيائية
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The subject of this thesis involves studying the possibility removed of four organic compound by TiO2. These organic compounds (considered as pollutants) which are; Birlliant blue (dye), polyvinyl alcohol (PVA), Linear alkyl benzene sulfonate (LAS) and Lambdacyholothrin as (pesticides). The thermal and photo - stability were studied and the results showed that all pollutants are stable in temperature range about (288 - 318) K, and stable against UV - linght in the wave length range (290 - 320) nm.Titanium dioxide successed in removing; 95 - 54% of dye, 6.2% of PVA, 13.19% of LAS and failed in removeing pesticides.UV - Vis absorption spectrophotometric technique was used to follow the pollutants concentration before and after adsorption process and after different periods of time, since the sorption isotherms were obtained by obeying Langmiur and Freundlich adsorption isotherms, with R2 (1 - 0.9993) for dye, R2 (0.9992 - 0.9574) for PVA, R2 (0.9503 - 0.9813) for LAS.The dye adsorption isotherms take S - shapes which related to a strong interaction between dye and TiO2 with thermodynamic values DH = +(5.962 - 26.57)J, DG = - (966 - 999)J, DS = +(3.45 - 9.1906)J.The thermodynamic parameters were studied by using the sorption process of the three pollutants on TiO2 of different temperatures ranging (293 - 318)K, and from the sorption isotherms the values of DH, DG, and DS for PVA DH = - (133.4 - 212.83)J, DG = +(78 - 157.4)J, DS = - (500)J, LAS DH = +(53.14 - 66.14)J, DG = - (1.21 - 1.38)kJ, DS = +(4 - 14)J. The sorption process of dye and LAS a positive DH values, negative DG values and positive DS values, which indicates the spontaneous absorption process, which for the negative DH values, positive DG values and negative DS values are due to the non spontaneous adsorption process for PVA. The kinetic study of pollutants sorption on TiO2 was studied depending on three kinetic equations : 1 - Lagergren equation : it was used to obtain the order of the sorption process, and the results showed a good obey with R2 = (0.9477 - 0.9995) for dye, R2 = (0.956 - 0.9942) for PVA, R2=(0.9948) for LAS, to this equation, which indicates that the sorption processfollowed a pseudo - 1st order kinetics, and from the linear Lagergren equation for the pollutants sorption the rate constants of sorption were calculated at different temperatures, and the activation energy for the sorption process was also calculated which reached 39.011 kJ.mol - 1 for sorption of dye.2 - Morris - Weber model : was employed and it gave a good match with the straight linear equation with R2 = (0.98 - 0.994) for dye, R2=(0.9892) for PVA, R2 = (0.9989) for LAS. This relation indicates that the diffusion process was so obvious, and it involvesthe transport of pollutant from the bulk solution into the TiO2 surface, which is considered the rate - limiting step. 3 - Reichenberg model : was employed and it gave a good linear relationship between Bt and time with acceptable correlation coefficient R2 = (0.9891) for dye, R2 = (0.9306) for PVA, R2 = (0.9776) for LAS.This relation indicates that the rate limiting mechanism is the absorption and the sorption process involving three steps : absorption, adsorption and desorption).

تحري الخواص الحرارية لبعض السوائل الايونية الحاوية على اليوريا والاستمايد Investigation of Thermal Properties for some Ionic Liquids containing Urea and Acetamide

اسم المؤلف: هدى سلام عبد
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Characterization of some room temperature ionic liquids (RTILs) as candidates for thermal storage media and heat transfer fluids in thermal applications were investigated. Five ionic liquids prepared from ammonium alum [NH4Al(SO4)2.12H2O] pronounced S, as inorganic salt with urea [NH2CONH2] pronounced U, or acetamide [CH3CONH2] pronounced A, as organic compounds, and aluminum nitrate [Al(NO3)3.9H2O] pronounced N with urea or acetamide compounds in different mole ratios were investigated alone and with addition of some improving materials to study their synergetic effect using thermo - gravimetric analysis (TGA), Differential Scanning Calorimetery (DSC), X - ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy and conductivity measurements. Thermo - physical properties such as enthalpy ΔH, heat capacity Cp and thermal energy storage capacity were determined. It was found that hydrated aluminum nitrate : acetamide (1 : 22 mole ratio, AN2IL) alone and hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) alone or with addition of some materials characterized with high density, chemical stability, heat capacity, thermal energy storage capacity and wide temperature range. The results indicated that ionic liquids alone or with addition of some materials could be considered as a promising candidate for liquid thermal storage media and heat transfer fluids.Studying the synergetic effect by addition of some alkali metal hydroxide (NaOH) with hydrated aluminum nitrate : urea (1 : 1.2 mole ratio, UNIL) and KOH with hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) ionic liquids increased thermal energy storage capacity of these ionic liquids, while the addition of NaOH to hydrated aluminum nitrate : acetamide (1 : 22mole ratio, AN2IL) gave less thermal stability and storage capacity of ionic liquid.Also addition of alkaline earth metal oxide MgO, CaO to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) and BaO to hydrated aluminum nitrate : urea (1 : 1.2 mole ratio, UNIL) decreased thermal stability, heat capacity and thermal energy storage capacity than ionic liquid alone.Moreover, addition of transition metal oxide (VOSO4.5H2O, CuO and ZnO) to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) increased thermal stability and storage capacity of hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL), while the addition of NiO to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) only improve thermal stability of ionic liquid

التثبيت الضوئي لمتعدد كلوريد الفانيل باستخدام معقدات مخلبية Photostabilization of poly(vinyl chloride) by chelate complexes

اسم المؤلف: علي نجاح حسن
اسم المشرف: عماد عبد الحسين يوسف السراج
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Five metal complexes of Cu(II), Cd(II), Zn(II), Ni(II) and Sn(II) with {4 - (Benzylidene - amino) - 5 - pyridin - 4 - yl - 4H - [1,2,4]triazole - 3 - thiol}, of Schiff base ligand (L), were prepared in alcoholic medium.The ligand (L) and its metal complexes were characterized qualitatively by using : FTIR, UV - visible spectroscopy, magnetic susceptibility, conductivity measurements and 1H NMR only for ligand. The ligand acted as bidentate which coordinated to the metal ions through sulphur and nitrogen of Azomethine group.According to the spectral data of the complexes a tetrahedral geometry was suggested for these complexes, except Cu(II) complex which exhibited octahedral geometry distorted to square planar structure.The metal complexes were used to enhance the photostabilization of PVC contains a concentration of ML2 0.5 % by weight. The photostabilization of PVC films were studied at room temperature under irradiation of light with λ=313 nmand an intensity of 7.75 X 10 - 7 einstein dm - 3 sec - 1.The photostabilization activity of these compounds was determined bymonitoring the carbonyl (ICO), polyene (Ipo) and hydroxyl (IOH) indices and weightloss method with irradiation time. It was found that the (ICO), (Ipo) and (IOH)indices values increased with irradiation time and this increase found to depends on the type of additives.The surface morphology for these films was studied during irradiation time.The changes in viscosity average molecular weight of PVC with irradiation time were also tracked (using THF as a solvent). The quantum yield of the chain scission (Φcs) of these complexes in PVC films was also evaluated.The following trend was obtained for the photostabilization effect on PVC films in presence of additives as shown below : CuL2 , CdL2 , ZnL2 , SnL2 , NiL2 Increasing the photostability According to the obtained experimental results, mechanisms were suggested, depending on the structure of the complexes.

الاكسدة الضوئية التحفيزية للفينول الاحمر على دقائق ثنائي اوكسيد التيتانيوم النانوبلوري Photocatalytic Oxidation of Phenol Red on Nanocrystalline TiO2 Particles

اسم المؤلف: احمـــد عبد الله حسين
اسم المشرف: هـــلال شهاب وهاب
الموضوع العام: علوم الكيمياء
السنة: 2014
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: انجزت هذه الدراسة البحثية للتفكك الضوئي للصبغة العضوية الفينول الاحمر كنموذج للملوثات الفينولية وذلك باستخدام ثنائي اوكسيد التيتانيوم النانوي المحضر مختبريا وفي وسط مائي.استخدمت تقنيات تشخيصية عديدة مثل المجهر الالكتروني الماسح وحيود الاشعة السينية ومطياف الانتشار الانعكاسي والمجهر الالكتروني التنافذي وطيف رامان لدراسة شكل السطح والحجم الحبيبي والمساحة السطحية وطاقة الفجوة لثنائي اوكسيد التيتانيوم النانوي المحضر. وجد ان متوسط حجم الحبيبة هو 9, 9.95, 11 نانو باستخدام مجهر الالكتروني الماسح, مطياف الانتشار الانعكاسي وحيود الاشعة السينية على التوالي.وتم كذلك احتساب المساحة السطحية وحجم المسامات باستخدام منظومةBET حيث كانت النتائج للمساحة السطحية 48 م2\غم وحجم المسامات 3.7 نانو مما يؤكد كون ثنائي اوكسيد التيتانيوم النانوي ذات مسامات صغيرة. ((mesoporos.تمت دراسة تاثير العديد من المتغيرات التجريبية على عملية التفكك الضوئي مثل كمية ثنائي اوكسيد التيتانيوم النانوي, حامضية المحلول, التركيز الابتدائي للفينول الاحمر, شدة مصدر التشعيع, الحجم الحبيبي لثنائي اوكسيد التيتانيوم النانوي واضافة المؤكسدات.ثبتت الظروف التجريبية المثلى لعملية التفكك الضوئي لصبغة الفينول الاحمر عند الدالة الحامضية 4.5 والتركيز الابتدائي للفينول الاحمر مساويا الى 10.3 ملغم\لتر وكمية المحفز ثنائي اوكسيد التيتانيوم مساويا الى 500 ملغم\لتر, حيث تم الحصول على ثابت سرعة التفاعل بقيمة 0.01052 لكل دقيقة وعمر نصف العملية 1.098 ساعة عند الظروف المثلى.اوضحت دراسة حركية التفكك الضوئي للفينول الاحمر بان العملية من الدرجة الاولى. اضافة على ذلك تم احتساب الناتج الكمي لعملية التفكك الضوئي حيث تساوي 0.1.اظهرت النتائج بان عملية الاكسدة الضوئية للفينول الاحمر بواسطة ثنائي اوكسيد التيتانيوم النانوي تفضل كيمياء الهيدروكسيل لانه عند اضافة بيروكسيد الهايدروجين حفزت عملية التفكك وتحسنت وتاكيدا على هذا الكلام عند اضافة ايزو بروبانول ثبطت عملية تفكك الفينول الاحمر لانه يعتبر من اهم المثبطات لجذر الهيدروكسيل. وتم كذلك احتساب الدوال الثرموديناميكية الاساسية لعملية التفكك الضوئي للفينول الاحمر مثل طاقة التنشيط وطاقة جبس والانثالبي والانتروبي. | In the current research study, the photocatalytic (photodecolorization) degradation of the phenolic model ecotoxicant, phenol red dye has been investigated using laboratory synthesized anatase TiO2 nanoparticles in aqueous solution. The prepared nano TiO2 powder has been characterized using several advanced instruments including, Scanning Electron Microscopy (SEM), Energy Dispersive X - Ray Spectroscopy (EDXS), X - Ray Diffraction (XRD), Diffused Reflectance UV - VIS spectrometry (DUR - UV - VIS), Transmission Electron Microscopy (TEM), Brunauer - Emmett - Teller (BET) theory and Raman Spectrometry. Average particle size of 9, 9.95 and 11 nm was found using TEM, XRD and SEM, respectively. The surface area and pore size were also measured employing BET nitrogen adsorption apparatus which resulted in surface area of 48 m2/g and a pore size of 3.7 nm, which indicates the mesoporosity of the prepared nano anatase TiO2 particles. The impacts of several operational parameters for the photodegradation process were explored encompassing, TiO2 loading, solution pH, initial phenol red concentration, UV light source intensity, photocatalyst particle size and added oxidants. Under optimum experimental conditions, 4.5 solution pH, 500 mg/l TiO2 loading and 2.9 x 10 - 5 mol /l (10.3 mg/l) phenol red, the value of the apparent rate constant, kapp , obtained has been 0.01052 min - 1 (17.53x 10 - 5 sec - 1) and the half life of the process, accordingly is equal to 1.098 hours.The kinetic of phenol red photobleaching has also been studied and it was found that it follows the pseudo first order pattern regardless of reaction conditions. Furthermore, the apparent quantum yield for the photodecolorization process was also determined and found to be approximately 0.1.Results reveal that the photooxidation process of phenol red follows hydroxyl type chemistry in which the addition of hydrogen peroxide has contributed massively in the promotion of the process rate and yield, and further, suppressed to a great extent by addition of isopropanol as .OH radical scavenger.The main process activation thermodynamic parameters namely, Gibbs energy, enthalpy and entropy were also deduced following the computation of photolysis activation energy employing the well known Arrhenius relation.

تحري قنص غاز ثاني اوكسيد الكربون بواسطة السوائل الايونية عند درجة حرارة الغرفة INVESTIGATION OF CO2 GAS CAPTURING BY ROOM TEMPERATURE IONIC LIQUIDS

اسم المؤلف: ايفون اكرم عبد الجبار
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2014
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Some ionic liquids were investigated for abilities to capture CO2 alone or with added some catalysts at room temperature under atmospheric pressure to increase the capacity of ionic liquids to capture carbon dioxide gas some catalysts were found effective such asHydrated aluminum nitrate/urea ionic liquid with added CaO and NaOH , monoethanolamine and ammonium chloride were added to hydrated ammonium aluminum sulphate/urea ionic liquid did not show in FTIR sign of either physical or chemical absorption of CO2 . The addition of NaOHaq to hydrated ammonium aluminum sulphate/urea ionic liquid showed a new vibration absorption at 1666 cm - 1 and changing the frequencies in the amine group vibrational bands above 3000 cm - 1 . While the distilled water when added to the ionic liquid hydrated ammonium aluminum sulphate/urea showed a broaden effect on the high vibrational bands above 2500 cm - 1 and the carbonyl group vibrational band at 1662 cm - 1 was not effected .Calcium oxide was added to hydrated ammonium aluminum sulphate/urea showed a new splitting vibration absorption bands at 1666 cm - 1 ,1618 cm - 1 .Aluminum chloride - urea ionic liquid very effective to capture carbon dioxide gas without add any catalysts showed a chemical absorption of CO2 1655 cm - 1 while aluminum chloride - acetamide showed weaker or no ability to capture CO2 .

تحضير معقدات لاعضوية مشتقة من 4 - امين - 5 - بيريدايل 4,2,1 ترايزول - 3 - ثايول ودراسة الثباتية الضوئية - 4H - لها لبوليمر البولي ستايرين Synthesis of inorganic complexes derived from 4 - amino - 5 - (pyridyl) - 4H 1,2,4 triazole - 3 - thiol and study their photochemical stability with polystyrene

اسم المؤلف: رغد علي عبد الرسول حداد
اسم المشرف: عماد عبد الحسين يوسف السراج
الموضوع العام: علوم الكيمياء
السنة: 2014
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Five transition metal complexes of Ni(II), Cu(II), Zn(II), Cd(II) and Sn(II) with {4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol}, as a ligand (L) has been prepared in alcoholic medium. These complexes are : 1. Bis(4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol) Nickel(II), Ni(L)2 .2. Bis(4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol) Cupper(II), Cu(L)2 .3. Bis(4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol) Zinc(II), Zn(L)2 .4. Bis(4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol) Cadmium(II), Cd(L)2 .5. Bis(4 - amino - 5 - (pyridyl) - 4H - 1,2,4 - triazole - 3 - thiol) Tin(II), Sn(L)2 .The ligand (L) and its metal complexes were characterized quantitatively and qualitatively by using : FTIR, UV - visible spectroscopy, 1H and 13C NMR, magnetic susceptibility and conductivity measurements. This ligand act as bidentate that coordinated to the metal ions through sulphur and nitrogen of amine group. According to the spectral data of the complexes a tetrahedral geometry was suggested for these complexes except Cu(II) complexes which exhibit a square structure.In this work the prepared complexes of 4 - amino - 5 - (pyridyl) - 4H 1,2,4 triazole - 3 - thiol were used to enhance the photostabilization of Polystyrene (PS).Polystyrene has been mixed with these complexes in chloroform solvent which containing concentration of complex 0.5 % by weight, which produced by the casting method from chloroform solvent. The photostabilization of polystyrene films were studied at room temperature under irradiation of light λ=365 nm wave length with intensity 20.6*10 - 9 Ein Dm - 3 S - 1 .The photostabilization activity of these compounds was determined by monitoring the carbonyl (ICO) and hydroxyl (IOH) indexes, weight loss method with irradiation time. It was found that the (ICO) and (IOH) indexes values increased with irradiation time and this increase depend on the type of additives. The surface morphology for these films was studied during irradiation time. The changes in viscosity average molecular weight of PS with irradiation time were also tracked (using chloroform as a solvent). The quantum yield of the chain scission (Φcs) of these complexes in PS films was also evaluated.The following trend is obtained for the photostabilization effect on PS films in presence of additives as shown below : Sn(L)2 , Cd(L)2 , Ni(L)2 , Zn(L)2 , Cu(L)2 Increasing the photostability According to the experimental results obtained, mechanisms were suggested, depending on the structure of the complexes

تصنيع ودراسة اقطاب بوليمرية جديدة لتقدير الكلاريثرومايسين Construction and study of new polymeric membrane electrodes for clarithromycin determination

اسم المؤلف: حيدر قيس منشد
اسم المشرف: خالدة حميد محمد السعيدي
الموضوع العام: علوم الكيمياء
السنة: 2013
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: This piece of research includes constructing and characterizing two kinds of ion - selective electrodes (ISEs) based on PVC matrix membrane.First, four ion - selective electrodes for clarithromycin (CLM) which based on clarithromycin - tetraphenylborate (CLM - TPB) ion - pair complex as the electro - active materials were prepared. Second, four ion - selective electrodes for clarithromycin which based on using clarithromycintetraiodomercurate (CLM - TIM) ion - pair complex as the electro - active materials were also prepared. In both kinds of ISEs, some of the selected plasticizers were employed such as; Di - octyl phthalate (DOP), Di - butyl phosphate (DBP), Acetophenone (AP) and Di - butyl phthalate (DBPH) in PVC matrix. This thesis has mainly been structured in three different chapters, each one containing the following information : Chapter one provides a short historical review with the analytical performance characteristics of ISEs are described. The applications of ISEs in pharmaceutical and clarithromycin analyses are well - arranged in tables and the general and specific objectives of thesis are reported. Chapter two corresponds to the experimental part. Reagents, instruments, procedures and detail protocols for the preparation of two kinds of ISEs used in this study are reported.Chapter three contains the experimental results and discussion that lead to the possibility of successful applications the constructed ISEs in pharmaceuticals preparation and clarithromycin measurements. It is reporting the construction of two kinds of larithromycin ISEs; The first kind ISEs were : CLM - TPB+DOP (E1), CLM - TPB+DBP (E2), CLM - TPB+AP (E3) and CLM - TPB+DBPH (E4), give the linear range from (1×10 - 5 - 1×10 - 3, 1×10 - 5 - 1×10 - 3, 5×10 - 5 - 1×10 - 3 and 1×10 - 5 - 1×10 - 3 M), the slopes of (51.206, 53.930, 58.104 and 58.484 mV/decade) respectively, with detection limits of (8×10 - 6, 6×10 - 6, 2×10 - 5 and 9×10 - 6 M), response time of 10 - 3 M (30, 35, 41 and 46 second) and the lifetime were about (24, 30, 12 and 20 days) respectively. The second, were : CLM - TIM+DOP (E5), CLM - TIM+DBP (E6), CLM - TIM+AP (E7) and CLM - TIM+DBPH (E8), give the linear range from (1×10 - 5 - 1×10 - 3, 5×10 - 5 - 1×10 - 3, 5×10 - 5 - 1×10 - 3 and 1×10 - 5 - 1×10 - 3 M), the slopes of (48.445, 42.970, 52.692 and 49.442 mV/decade) respectively, with detection limits of (5×10 - 6, 5.5×10 - 5, 5×10 - 5 and 1.5×10 - 5 M), response time of 10 - 3 M (26, 32, 30 and 48 second) and the lifetime were about (28, 22, 16 and 25 days) respectively.The best electrode is (E4) used to determine the clarithromycin in pure and pharmaceuticals samples. The working pH for (E4) electrode was ranged from (1.5 - 6.5), the selectivity coefficients (Kpot A,B) of ISEs for the CLM have been studied in the presence of interference ions (Na+, K+, Mn+2, Cu+2, Fe+3, Al+3, sucrose and gelatin) by using separated solution and fixed interfering methods and the results was ranged from (4.28×10 - 2 - 8.82×10 - 5), which revealed that there was no effect of the interferences on the determination of CLM in tablets by using the constructed ISE.Therefore the ISE (E4) gave a good electrochemical characterization among the others and it has been used successfully for the determination of clarithromycin in the Claricide tablets using different potentiometric methods.

دراسة طيفية لبعض املاح العناصر الانتقالية في السائل الايوني SPECTROSCOPIC INVESTIGATION FOR SOME TRANSITION METAL SALTS IN IONIC LIQUID

اسم المؤلف: مروة حميد فاضل
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2013
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Aluminum chloride - urea ionic liquid was investigated by Lewis acid - base titration with chloride ions for its active species concentration with the aide of electronic spectroscopy. A coordination bonds between aluminum cationic species of the ionic liquid and the aromatic ring of toluene or benzene was assumed to be responsible for new bands formed in visible and ultraviolet regions.Upon Lewis acid - base titration these bands was found to disappear and the concentration of the acidic species therefore was elucidated to be around 75 mole % of the initial aluminum chloride used to prepare a 1.5 mole aluminum chloride to 1 mole urea ionic liquid. The product of this reaction was assumed to be between mole acidic species to mole chloride ion according to the mole fraction elucidated graph.The behavior of some transition metal compounds (chlorides and sulfates) of (Cu(II), Co(II) and Ni(II)) coordination in the ionic liquid was also investigated in this ionic liquid by electronic spectroscopy. Cobalt chloride showed a different behavior than the distorted octahedral geometry of copper chloride as it reacted with the anionic species to precipitate as form of a tetrahedral complex containing urea, aluminum and chloride ions.The behavior of nickel sulfate in the ionic liquid also showed an acid - base reaction with the acidic species of ionic liquid as the bands at 334 nm and 474 nm decreased with increasing the salt concentration. The coordination of Ni(II) cation was found to be an octahedral geometry with stronger ligand field effect. Similar strong ligand field was also observed with copper sulfate which showed four bands resulted from separating metal d - orbitals more obviously than the tetragonal John - Teller effect found with copper chloride in same ionic liquid.

الخواص الثرموديناميكية والحجمية لبعض الفيتامينات الذائبة - مائيا في حامض الهيدروكلوريك المخفف وكذللك في المحاليل المائيه لملح كلوريد الصوديوم عند درجات) 51.392 و51.392 و1.392 . و1.392 . (كلفن Thermodynamic and Volumetric Properties of Some Water - Soluble Vitamins in Dilute HCl and in Aqueous NaCl Solutions at (293.15, 298.15, 303.15, and 308.15) K

اسم المؤلف: خطاب عدنان عبد
اسم المشرف: تغريد علي سلمان
الموضوع العام: علوم الكيمياء
السنة: 2012
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Densities , ρ, and viscosity, η, have been measured for ascorbic acid, thiamin HCl, nicotinic acid and pyridoxine HCl have been measured in water and in aqueous sodium chloride solutions at (293.15, 298.15, 303.15 and 308.15) K. The apparent molar volumes were determined from the measured density data. These volumes were extrapolated to zero using suitable empirical or theoretical equations to determine the corresponding infinite dilution values.Ionization of the vitamins under studied were suppressed using sufficiently acidic solutions. Apparent molar volume at infinite dilution for all vitamins, were found to be increase with increasing temperature in acidic solution and the presence of co - solute NaCl. On the other hand, increasing the concentration of co - solute NaCl leads to decrease the apparent molar volumes. These results were interpreted in terms of complex vitaminswater - co - solute NaCl interactions.Apparent molar volumes of transfer at infinite dilution for vitamins from water solutions to NaCl solution at various temperatures in the range (293.15 - 308.15) K were calculated. The resulting data have been utilized to the effect of overlapping of the hydration co - spheres on net volume of vitamins. The viscosity data have been analyzed using Jones - Dole equation, and the derived parameters, Jones - Dole coefficient, B, and Falkenhagen coefficient, A, were interpreted in terms of solute - solvent and solute - solute interactions respectively, for ascorbic acid, thiamin HCl, nicotinic acid and pyridoxine HCl. The variation of B coefficient with temperature, (dB/dT), have been also calculated for vitamin solutions, and the obtained data was interpreted on the basis of the structure - making and structure - breaking behavior.Free energy of activation of viscous flow per mole of solvent, Δμ1°, and solute, Δμ2°, were obtained by application of the transition - state theory to the B coefficient data and the corresponding activation enthalpy, ΔH0, and entropy of activation, ΔS0, of viscous flow were also determined for vitamins.

مثبتات ضوئية جديدة لبولي كلوريد الفانيل باسخدام بعض ايونات العناصر لمعقدات2 - 6 - ميثوكسي نفثالين - 2 - وايل بروبانويت

اسم المؤلف: حسام اكريم سلمان
اسم المشرف: عماد عبد الحسين يوسف السراج جواد كاظم شنين
الموضوع العام: علوم الكيمياء
السنة: 2012
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The preparation of Bis[2 - (6 - methoxynaphthalen - 2 - yl)propanoate] chelate complexes with nickel(II), copper(II), zinc(II), cadmium(II) and tin(II) were described in this thesis.Infrared, ultraviolet - visible, spectrophotometric techniques, magnetic susceptibility, atomic absorption, conductivity measurements and melting point were used to characterize the free ligand and the above chelate complexes. All these complexes were found to act as stabilizer in PVC films.The light of wavelength (313 nm) with intensity of (1.052×10 - 8 ein.dm - 3.S - 1) was used for irradiation of polymer films at room temperature. The rate of photodegradation and photostabilization of PVC film (thickness 30 m) were monitored by measuring the carbonyl, polyene, hydroxyl and chlorine indices (Ico, Ipo, IoH and Icl) values as a function of irradiation time and ultraviolet - visible spectrophotometry using 0.5% wt/wt concentration of stabilizer.It was found that the carbonyl index (Ico), polyene index (Ipo) and hydroxyl index (IoH) values increased with irradiation time, while the chlorine index (ICl) values decreased with irradiation time, and this increase depend on the type of additives (free ligand and complexes).The following trend was obtained for the photostabilization effect of PVC film in presence of these additives : Cd(L)2 > Zn(L)2 > Sn(L)2 > Ni(L)2 > Cu(L)2.According to the experimental results obtained several mechanisms were suggested depending on the structure of the additives. Among these mechanisms, HCl scavenging, UV absorption, peroxide decomposer and radical scavenger for photostabilizer additives.The mode of chain scission was also investigated by measuring the variation of average viscosity molecular weight with irradiation time for PVC films with and without additives. It was found that the values of the variation of average viscosity molecular weight decreased with increasing irradiation time

تحليل الطيف الالكتروني لمركبات ايونات بعض العناصر الانتقالية في سائل ايوني جديد

اسم المؤلف: زينة نذير رجب
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2012
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The behavior of some transition metal cations [Cr (III), Fe (III), Fe (II), Co (II), Ni (II) and Cu (II)] were investigated in ammonium alum - urea ionic liquid. The study was followed by UV - Visible electronic spectroscopy to establish their coordination geometry in the liquid and estimate the ionic species attached to the transition metal cations.The reactivity of the metal cations were found to vary from one to another. Chromium (III) cation was found, (as expected) to be in octahedral geometry with ionic liquid species and was inert toward the addition of ligands. Similarly iron (III) did not show a tendency to react with added ligands, yet charge transfer was prevailed. However, interesting iron (II) showed high spin octahedral coordination with thiocyanate ion but a low spin octahedral complex with nitrite ion.Cobalt (II) showed an interesting behavior in alum - urea ionic liquid, as it coordinated in an octahedral geometry with its ionic species. A gradual geometrical changes were appeared as a major change in their spectra most probably forming a mixture of two species tetrahedral with some original octahedral complex when its solution was studied with increasing thiocyanate ion concentration up to 35 thiocyanate : 1 cobalt mole ratio.The solubility limit of nitrite in ionic liquid ceased the concentration ratio of nitrite : cobalt to be 5 : 1.Nickel (II) also showed an octahedral geometry behavior in ionic liquid species. It reacts with added ligands particularly when theconcentration of thiocyanate ion : Ni (II) increased up to 30 to 1 mole ratio, the color changed from pale green to olive - green solution.Cupper (II) cation showed a clear blue solution and its spectra are assigned to be octahedral geometry, while the added nitrite did not show color change but less absorbance was recorded. However, thiocyanate ion seems to react with cupper (II) ionic liquid solution producing suspended green solution with much less absorbance than with ionic liquid.Interestingly, the water molecules present in the original ammonium alum was not found to coordinate with metal cations as their spectra was found to differ when compared with those obtained in aqueous solution.

تصنيع اقطاب انتقائية جديدة لتقدير كل من الكلور امفينيكول صوديوم ساكسينيت والحديد الثلاثي وتطبيقاتها في المستحضرات الصيدلانية Construction of new Ion Selective electrodes for Determination Chloramphenicol sodium succinate and Iron(III) and their applications in pharmaceutical samples

اسم المؤلف: وئام رعد عزيز
اسم المشرف: خالدة حميد محمد السعيدي
الموضوع العام: علوم الكيمياء
السنة: 2011
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Two kinds of electrodes were prepared in this study based on PVCmatrix. Four ion selective electrodes for Chloramphenicol sodiumsuccinate which based on chloramphenicol palmitate (CPP) and sodiumtetraphenylborate (TPB) as additive, Another Four ion selectiveelectrodes for Iron(III) based on Chloramphenicol sodium succinate - Iron(III) [CPSS - Fe(III)] ion - pair complex as the electro - active material,.Many plasticizers used :  Di - butyl phthalate (DBPH) Di - butyl phosphate (DBP) Di - octyl phthalate (DOP) Tri - butyl phosphate (TBP)The electrodes parameters were include, linear concentration range,Nernestian slope, limit of detection, response time, life time, working pHrang and selectivity were evaluated. Also the statistical treatments wereapplied for the results that include : relative standard deviation (RSD),relative error (RE), error and confidence limit for concentration. The resultsshowed : 1 - ISES for Chloramphenicol sodium succinate : CPP+TPB+DBPH (membrane A1), CPP+TPB+DBP(membrane A2),CPP+TPB+DOP (membrane A3), CPP+TPB+TBP (membrane A4), givesthe slopes (53.98, 51.45, 49.66 and 48.98 mV/decade), linear range from(1x10 - 4 - 1x10 - 1, 5x10 - 4 - 1x10 - 1, 1x10 - 4 - 1x10 - 1, 5x10 - 4 - 1x10 - 1), withdetection limit (5x10 - 5M, 2x10 - 5 M, 3x10 - 5 M and 1x10 - 5 M), responsetime of 10 - 3M (15, 18, 20 and 35 second) and the lifetime were about (50,15, 23 and 21 day ). The working pH ranges were ranged from (2 - 7.5).The electrode A1 (CPP+TPB+DBPH) has been used to determineVIChloramphenicol sodium succinate in the pharmaceutical samples of(Chloramphenicol sodium succinate injection).2 - ISES for Iron(III) : CPSS - Fe(III)+DBP (membrane B1), CPSS - Fe(III)+DBPH (membraneB2), CPSS - Fe(III)+DOP (membrane B3) and CPSS - Fe(III)+TBP(membrane B4), gives the slopes (19.79, 26.60, 16.01 and 13.82), linearrange from (1x10 - 5 - 1x10 - 2 M, 1x10 - 5 - 1x10 - 2 M, 1x10 - 6 - 1x10 - 2 M and1x10 - 5 - 1x10 - 2 M), with detection limit (9×10 - 6 M, 7×10 - 5 M, 2×10 - 6 Mand 9×10 - 5 M), response time of 10 - 3 M (10, 35, 15, 35 and 30 second),lifetime were about (37, 41, 23 and 16 days). The working pH rangeswere ranged from (2 - 6) by using electrode (CPSS - Fe(III)+DBP), andthis electrode has been used to determine Iron(III) in the pharmaceuticalsamples of (Feroglobin Capsules).The selectivity coefficients (KpotA,B) of ISES have been studied for thefollowing interference ions (Na+, K+, Mn+2, Cu+2, Zn+2, Fe+3, Al+3,Chloramphenicol palmitate, folic acid , Sucrose and Gelatin) by usingseparate solution method and fixed interfering mixed method.The UV - spectrophotometric method which includes : - The derivative spectra, the first - derivative (1D) spectra for Chloramphenicol sodium succinate solutions (2 - 64 mg/L) in wavelength equal 258 nm with (r2=0.99925). The analytical methods results showed to be simple, rapid and with a good accuracy by comparing between FirstDerivative (1D) and direct method of Ion selective electrode by using Ftest.The results shown, that the Chloramphenicol sodium succinate can be determined by using Ion selective electrode method because the value of the (F) experimental less than the value of the (F) theoretical at 95% confidence limit. Since Fcalculated‹ Ftable, we oncluded that there is nosignificant difference in precision between two methods

دراسة الذوبان والكيمياء التناسقية لاكاسيد بعض العناصر الانتقاليه للمنصهر الايوني المحضر لمزيج كلوريد الكولين / حامض التارتاريك Solubility and coordination study of some transition metal oxides in new choline chloride/ tartaric acid ionic liquid

اسم المؤلف: فرح انور حسن
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2008
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: في هذا البحث تم تحضير نوع جديد من الاملاح المنصهرة في درجة حرارة الغرفة , عن طريق مزج احد املاح جذر الامونيوم الرباعي وهو كلوريد الكولين مع احد المواد لها القابلية على تكوين اواصر هيدروجينية وهو الحامض الكاربوكسيلي الثنائي الكاربوكسيل وهو حامض التارتارك, تم تحضير عده محاليل بنسب مولية مختلفة. ومن المخطط الطوري للمحلول تم الحصول على محلول بدرجه انصهار 5 درجه مئوية.ومن مواصفات هذا الملح المنصهر المحضر هي : له صفات توصيلية , له كثافة عالية , وقيمه الاس الهيدروجيني له واطئه. وايضا في هذا البحث استخدمه الملح المنصهر المحضر كمذيب لا مائي لدراسة قابليه ذوبان بعض اكاسيد العناصر الانتقاليه من السلسلة الاولى وتشمل : [Co3O4, CrO3, NiO, CuO, ZnO]حيث وجد ان لها القابليه على الذوبان في هذا الملح المنصهر المحضر, وتم قياس التركيز ( الاذابة ) عن طريق استخدام جهاز الامتصاص الذري وذالك بدرجه حرارة الغرفه صعودا الى المائة درجة مئوية.اضافة الى ذلك تم حساب الحرارة الكامنة للانصهار لكل واحد من اكاسيد العناصر وتم توضيح تاثير اوربيتال d على قيمة الحرارة الكامنة للانصهار. تم تشخيص المحاليل السابق ذكرها عن طريق جهاز الاشعة الفوق البنفسجية - المرئية (UV. Vis.) لغرض معرفه المعقدات المتكونة ومعرفة التغير في الصيغة التركيبية للاوكسيد . وتم اخذ بنظر الاعتبار تاثير زيادة الحرارة الى درجه حرارة مائه درجه مئوية , حيث ان زيادة درجه الحرارة ليس له تاثير على الصيغه التركيبية الا انه له تاثير على زيادة الاهتزاز الالكتروني. تم حساب معامل راكاح (Racah) ,مقاييس المجال الليكندي , مقدار طاقه الانفصال (Δo) وحساب الامتصاصية المولاريه لكل طيف في جميع درجات الحرارة. | Choline chloride / tartaric acid room temperature ionic liquid was prepared and the obtained phase diagrams of the mixture showed eutectic point at 5 oC. The ionic liquid showed a conductive properties, high density and low PH values. Secondly, the dissolution of Co3O4, CrO3, NiO, CuO, and ZnO. Were studied and found soluble in choline chloride / tartaric acid ionic liquid as their solubilities were determined by measuring the dissolved metal by atomic absorption from room temperature up to 100 oC. The lattice energies of the metal oxides were deduced and the effects of the d - orbital electrons on the lattice energy were compared. In addition to their solubilities the above solution of metal oxides were investigates by ultraviolet visible spectroscopy. The spectra were measured and assigned to the expected coordination in the choline chloride/ tartaric acid ionic liquids, the effect of increasing temperature of the solution up to 100 oC were also studied and showed similar coordination but higher vibration with increasing temperature. Racah factor for there complexes (B) were determined together with field factor, crystal field splitting energy (Δo), nephelauxetic factors and molar absoptivities for each spectra at the variable temperatures.

تحضير وتشخيص الاملاح المنصهرة (السوائل الايونية) المستندة على مركبات السلفونيت Preparation and Characterization of Molten salts (Ionic Liquids) Based on Sulfonate Compounds

اسم المؤلف: عهد ديوان ساجت الفتلاوي
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2008
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: تضمنت الرسالة دراسة تحضير وتشخيص املاح منصهرة (سوائل ايونية) تكون منصهرة في درجة حرارة الغرفة حيث تم تحضير كولين دودوسيل بنزين سلفونيت وفينل تراي ميثل امونيوم دودوسيل بنزين سلفونيت وكانت درجة الانصهار لكل منهما هي,118) oC ( 91.9 على التوالي .تم تحضير املاح منصهرة (سوائل ايونية) اخرى بواسطة خلط , صوديوم دودوسيل بنزين سلفونيت , بوتاسيوم دودوسيل بنزين سلفونيت, امونيوم دودوسيل بنزين سلفونيت , بنزويك اسد, ساليسالك اسد مع الكولين كلورايد وقد اظهرت عملية الخلط انخفاض كبير درجة الانصهار عن للمركبات الاصلية.الخليط المكون من( امونيوم دودوسيل بنزين سلفونيت\ الكولين كلورايد) ينصهرعند 15 oC , ايضا خليطي (بنزويك اسد\ الكولين كلورايد ( و) ساليسالك اسد\ الكولين كلورايد ( مع لهما درجة انصهار متشابهة مقدارها 60 oC , وهذة الدرجة تنطبق مع تعريف الاملاح المنصهرة (السوائل الايونية) التي تنصهر في درجة حرارة افل من oC 100, لذلك تعتبر املاح منصهرة في درجة حرارة الغرفة. اظهرت الخلطات المكونة من (صوديوم دودوسيل بنزين سلفونيت\ الكولين كلورايد) و(بوتاسيوم دودوسيل بنزين سلفونيت \ الكولين كلورايد) درجات انصهار اعلى من oC 100 . مجموعة اخرى من الاملاح المنصهرة (السوائل الايونية) التي تم تحضيرها بواسطة خلط نفس المركبات السابقة لكن مع اليوريا بدلامن الكولين كلورايد هذة الاملاح المنصهرة (السوائل الايونية) المكونة من مركبات السلفونيت لهما درجات انصهار اقل مما للاملاح المنصهرة المعتمدة على الكولين كلورايد التي تنصهر عند105 oC , oC 100 , 10 oC على التوالي. بينما في حالة )بنزويك اسد\ اليوريا ( و) ساليسالك اسد\ اليوريا ( تنصهر بدرجات اعلى وكانت, oC 75 , oC 77 على التوالي. الاملاح المنصهرة (السوائل الايونية) تتكون نتيجة التداخل الذي يحصل بين مكونات الخليط وتكون تاصرهيدروحيني او تكون معقد بين مكونات الخليط | The work presented in this thesis includes the preparation and characterization of choline dodecyl benzene sulfonate and phenyl trimethyl ammonium dodecyl benzene sulfonate, which were prepared and showed almost room temperature molten salts (ionic liquids) of 118 oC and 91.9 oC respectively, as shown in scheme (1) : Scheme (1) Other molten salts (ionic liquids) based on mixing sodium, potassium, ammonium dodecyl benzene sulfonate, benzoic acid and salicylic acid with choline chloride showed a larger melting point depression than from of initial components, as shown in scheme (2) and (3) : Scheme (2) (Ammonium dodecyl benzene sulfonate /choline chloride) mixture has a deep eutectic point of 15 oC, while the two mixtures (benzoic acid / choline chloride) and (salicylic acid / choline chloride) gave a similar eutectic point of 60 oC, which were correspond with the room temperature molten salt (ionic liquids) definition, which is melt below the 100 oC. However, (sodium dodecyl benzene sulfonate /choline chloride) mixture and (potassium dodecyl benzene sulfonate /choline chloride) mixture afforded higher eutectic temperature than the room temperature molten salts.Another set of mixtures that based on mixing the same previous compounds, but with urea instead of choline chloride. These mixtures showed with (NaDBS,KDBS and NH4DBS) compounds lower eutectic points than with choline chloride of 105 oC, 100 oC, and 10 oC respectively. While with benzoic acid and salicylic acid afforded a little higher temperature of 75 oC and 77 oC respectively. Compositions of these mixtures attributed to the formation and interaction of hydrogen bonding or the formation of complex compounds of eutectic nature.

الفصل الكروموتوغرافي لبعض الايونات الموجبة وتقديرها بواسطة كاشف التوصيلية والتحليل الضوئي غير المباشر

اسم المؤلف: لبنى عبد الحسين عبد الامير الشيخ
اسم المشرف: شهباز احمد مكي
الموضوع العام: علوم الكيمياء
السنة: 2007
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Cation exchange chromatography with both unsuppressed conductivity detection and indirect photometric detection (IPD) modes were used for the separation and detection of inorganic cations. Salt of weak base diphenylamine has been used as an eluent for several cations both with unsuppressed conductivity detection and IPD. 4 - aminodiphenylammonium chloride possess ion exchange capability, chromatographic selectivity and large molar absorptivity. 4 - aminodiphenylammonium chloride showed a good chromatographic performance toward the analysis of the cations (Lithium, Barium, Iron II and Iron III ) using conventional HPLC equipment with either conductivity or indirect UV detectors. The analysis of these cations using (1×10 - 7 M) 4 - aminodiphenylammonium chloride at pH 5.80 in 5% DMSO, with Dionex Ion Pac CS3 Column, and 1ml/min flow rate was achieved with unsuppressed column conductivity and IPD at 342.5 nm detection. Chromatogram of a separation mixtures containing four cations (Li+, Ba+2,Fe+2 and Fe+3) and other mixture have given well separated peaks using IPD technique. The capacity factor K for the analyzed cations were ranged from (1.70 - 2.44), peak symmetries was ranged from (1.11 - 1.41) and resolution with an average value of (1.310) was optained. The average RSD for tR was 0.435%. The average recovery was 93.1075 % and the average relative error percentage was 6.77 % with unsuppressed conductivity detection . However, using IPD, the peak symmetry was ranged from(1.30 - 1.54), and an average value of resolutin of 1.41 which indicate a good chromatographic performance. The RSD in tR averaged 0.351 %. The average value of recovery was 95.975 %. Calibration curve for all analyzed cations were linear from their detection limit to at least 10 ppm. The correlation coefficients for the linear calibration curve were ranged from (0.9991, 0.9998) with both detection techniques. The detection limit was ranged from (0.025, 0.1) ppm for unsuppressed conductivity detection compared to (0.02, 0.05) ppm for IPD

التثبيت الضوئي لمتعدد (كلوريد الفانيل) باستعمال معقدات ثئاني (2 - امينو خلات بنزوثايزول) PHOTOSTABILIZATION OF POLY(VINYL CHLORIDE) BY BIS(2 - AMINO ACETATE BENZOTHIAZOLE ) COMPLEXES

اسم المؤلف: هدیل عادل عباس
الموضوع العام: علوم الكيمياء
السنة: 2008
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: In this work , Bis(2 - amino acetate benzothiazole) chelate complexes were prepared . These compounds are : 1 - Bis(2 - amino acetate benzothiazol) nickel(II).2 - Bis(2 - amino acetate benzothiazol) copper(II).3 - Bis(2 - amino acetate benzothiazol) zinc(II).4 - Bis(2 - amino acetate benzothiazol) cadmium(II). 5 - Bis(2 - amino acetate benzothiazol) tin(II).Infrared, ultraviolet - visible, spectrophotometric techniques, magneticsusceptibility, atomic absorption conductivity measurement and other physical properties were used to characterize the free ligand and the above chelate complexes.All these compounds were act as stabilizer in PVC films.The rate of photodegradation and photostabilization of PVC film (thickness 30mm) were monitored by measuring the carbonyl, polyene and hydroxyl indices (Ico, Ipo and IoH) values as afunction with irradiation time and ultraviolet - visible spectrophotometry using the concentrations of additive 0.5% wt/wt. The light of wavelength 313 nm with intensity (1.052*10 - 8 ein.dm - 3.S - 1) was used for irradiation of polymer films at room temperature.It was found that the carbonyl index (Ico) polyene index (Ipo) and hydroxyl index(IoH) values increased with irradiation time, and this increase depend on the type of additives (free ligand and complexes). The following trend was obtained for the photostabilization effect of PVCfilm in presence of these additives : Sn(H)2 > Cd(H)2 > Ni(H)2 > Zn(H)2 > Cu(H)2. According to the experimental results obtained several mechanisms were suggested depending on the structure of the additives. Therefore HCl scavenging, UV absorption, peroxide decomposer and radical scavenger for photostabilizer additiveswere suggested.

تحضيـروتشخيص مركبات مقلدة للانسولين SYNTHESIS AND CHARACTERIZATION OF INSULIN - MIMETIC COMPOUNDS

اسم المؤلف: عمار جهاد صادق العبدلي
اسم المشرف: اياد حمزة جاسم
الموضوع العام: علوم الكيمياء
السنة: 2007
الموضوع الدقيق: الكيمياء
الدرجة: دكتوراه
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: تهيئ الكيمياء اللاعضوية مجالا خصبا لتصميم وتحضير مركبات صيدلانية لمعالجة الامراض العسيرة المعالجة في الوقت الحالي.منذ فترة طويلة استخدمت الادوية الفلزية لعلاج واعادة وظيفة فسلجة الجسم الى حالتها الاولية.ان عنصري الفناديوم والكروم يقدمان حالة مدهشة من بين العناصر الانتقالية حيث لها سلطة وصفة كيموفيزيائية نكشف من خلالها صفة مهمة كمقلدات لعمل الانسولين. ولهذا تم دراستها جيدا في علاج مرض السكري للنوع الاول والثاني.ان تصميم الادوية الفلزية في بحثنا يقيم بالدرجة الاولى بالتشابه الفراغي للاعمال السابقة والتركيب المبسط وصفة التواجد البايولوجي والذوبانية والامتصاصية.تم تحضير اربعة مركبات مختلفة لتتاصر مع فلزات VO (II) وCr (III) الايونية لتكون ثمانية معقدات مختلفة تم اختيار ستة احماض امينية مختلفة لتتاصر مع فلزات VO (II) وCr (III) الايونية لتكون اثنا عشر معقد مختلف تم اختيار الماركبتو حامض الخليك وحامض المانديلك للتاصر مع فلزات VO (II) وCr (III) الايونية لتكوين اربع معقدات مختلفة.تم اختيار خمسة سكريات مختلفة لتتاصر مع فلزات VO (II) وCr (III) الايونية لتكون عشرة معقدات مختلفة.تم عزل وتشخيص عدد من المركبات المختلفة عن طريق دراسة صفاتها الكيموفيزيائية بواسطة تحليل المعادن وتحليل عناصر C.H.N.S، واطياف التردد والانتقالات الالكترونية، والصفات التوصيلية والمغناطيسية، بالاضافة الى دراسة اطياف الرنين المغناطيسي النووي للهيدروجين.تمت دراسة تكوين بعض المعقدات في المحلول باتباع طريقة النسبة المولارية mole ratio.ان نتائج الدراسات في الحالة الصلبة والسائلة اعطتنا نتائج متطابقة. | Biomedical inorganic chemistry offers the potential for the design novel therapeutic agents for the treatment of diseases, which are currently intractable. Therapeutic metalodrugs have since long been employed to restore human physiology. Vanadium and chromium presents an outstanding case of a transition elements, the omnipotent physicochemical properties of which have unearthed it’s potential use as a serious insulin mimtic agents, well suited in the treatment of the heterogeneous disease of diabetes mellitus types I and II.The design of such metallodrugs has been at the fore front of the research depending on analogy of the previous work, simple structure, bioavailability, solubility and absorption property.Four different analog ligands have been synthesized to coordinate with VO (II) and Cr (III) metal ions to produce eight different complexes.Six different amino acids have chosen to coordinate with VO (II) and Cr (III) metal ions to produce twelve different complexes.Marcapto acetic acid and mandelic acid are also chosen to coordinate with VO (II) and Cr (III) metal ions to produce four different complexes.Five different sugars have been chosen to coordinate with VO (II) and Cr (III) metal ions to produce ten different complexes.Several of the synthesized compounds were isolated and characterized by studying their physicochemical properties such as C.H.N.S and metal analysis, vibrational and electric spsectra, conductivity, magnetic properties, in addition to 1H.N.M.R spectral study for some complexes.The formation of some of the complexes were studied in solution following the mole ratio method. The results of both solid state and solution studies gave identical results.

التقدير الطيفي لايون النحاس بوساطة الطريقة المباشرة وغير المباشرة بنقطة الغيمة باستخدام الحامض الامينيي الميثيونين Spectrophotometric Determination of Copper Ion by Direct Method and Indirect Cloud Point Using the Amino Acid Methionine

اسم المؤلف: اسماء نهاد زكي
اسم المشرف: رافع قدوري عطيوي سمية محمد عباس
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: تشمل هذه الدراسة طريقتين مهمتين في التطبيق التحليلي لتعيين وفصل واغناء ايون النحاس الثنائي بطريقة نقطة الغيمة والطريقة الطيفية وذلك باستخدام مطياف الاشعة الفوق البنفسجية - المرئية. في الجزء الاول : تم استخدام الحامض الاميني الميثونين ككاشف تحليلي الذي يشكل مركب مخلبي مع ايون النحاس في الطور المائي وبدرجة حموضة محددة, والذي تكون له اعظم امتصاصية عند طول موجي (244 نانوميتر) لمعقد النحاس - الميثونين ضد الميثونين كبلانك.وتم دراسة الظروف الفضلى للتفاعل بالاضافة الى العوامل التحليلية الاخرى وافضل نتائج تم الحصول عليها لمنحني المعايرة والبيانات الاحصائية تحت الظروف الفضلى التي تم الحصول عليها بالطريقة الطيفية المباشرة لكميات صغيرة من النحاس, يطاوع قانون لامبرت بير في مدى تراكيز (0,1 - 10) ميكروغرام/مل مع امتصاصية مولارية (5842 لتر.مول - 1.سم - 1) وحد الكشف (0,0238 ميكروغرام/مل) في هذه الدراسة لوحظ حدوث تداخلات بعض المعادن مثل النيكل (II)والكروم(III) في ايون النحاس وقد تجاوزت الحد المسموح للتداخل , لذلك تم تطبيق الطريقة المقترحة بنجاح لتحديد ايون النحاس في عينات مختلفة من المياه.اما الجزء الثاني من الدراسة تستند على تكوين معقد كاره للماء بين ايون النحاس والميثونين الغنية بالترايتون 100 - X من خلال منهجية الاستخلاص بنقطة الغيمة الى جانب القياس الطيفي للاشعة فوق البنفسجية - المرئية, في هذه الطريقة يتشارك ايون الفلز مع الحامض الاميني الميثونين في تفاعل لتشكيل معقد مخلبي كاره للماء ويتم استخلاص هذا المعقد في درجة حموضة معينة عن طريق الاستخلاص بنقطة الغيمة باستخدام المركب السطحي غير الايوني ترايتون 100 - X كوسيط للاستخلاص.الطور العضوي الغني بالمادة السطحية يتم اذابتها باضافة الميثانول ويتم قياس المعقد طيفيا عند طول موجي (294 نانوميتر) لتحسين العوامل التي تؤثر على كفاءة استخلاص ايون النحاس باستخدام احد عوامل التحليلية وتشمل هذه العوامل درجة حموضة المحلول تركيز الليكند والمادة السطحية, درجة الحرارة والوقت التي تم تحديدها بالاضافة الى الكتيونات التي تعتبر متداخلات في ظل الظروف المثلى للتفاعل وقد تحقق عامل اغناء النحاس وكان منحني المعايرة الخطي (0,1 - 4) ميكروغرام/مل, حد الكشف والحد الكمي (0,0071) (0,0215) على التوالي. وتم مقارنة الطريقة المقترحة مع الطريقة الطيفية المباشرة لتعيين ايون النحاس ومن خلال النتائج المعروضة نلاحظ اختلافات كبيرة في الدقة والتوافق في الطريقتين وان الاستخلاص بنقطة الغيمة هي الاكثر دقة وتوافقية. تم تطبيق هذه الطريقة في عينات المياه. في هذه الدراسة تم تعيين تكافؤية المعقد عن طريق النسب المولية, التغيرات المستمرة (طريقة جوب) في درجة حموضة معينة واظهرت النتائج ان نسبة التكافؤ بين ايون النحاس الميثيونين هي 1 : 2. | This study in whole comprises two significant approaches in analytical application for direct determination and separation with preconcentration of copper ion by cloud point extraction methodology coupled with UV - Visible spectrophotometry.In the first part : The amino acid methionine was used as a chelating agent to form a complex with copper ion in aqueous phase at specific pH, which exhibits maximum absorption at (max= 244nm) against reagent blank. The optimum reaction conditions and other analytical parameters were evaluated. The results showed better optical characteristics for calibration curve and statistical data were obtained under optimum conditions using direct Spectrophotometric determination of micro amounts of copper ion. “Beer's law” is obeyed in the concentration range (0.1 - 10)g.mL - 1 , having molar absorptivity of 5842L. mol - 1. cm - 1. The value of detection limit was 0.0238g.mL - 1 . Interference study indicated that some metal ions like Ni+2, Cr+3 have exceeded the allowable limits of interference for copper ion absorbance signal. The proposed method was applied successfully for the determination of copper ion in various water samples.Part Two : Deals with the formation of a hydrophobic complex between copper ion and methionine in rich - surfactant phase, by “cloud point extraction” (CPE) methodology, coupled with UV - Visible spectrophotometry. This method involved reaction of copper ion with methionine as a chelating agent to form a hydrophobic complex. Which was extracted at specific pH by CPE technique using nonionic surfactant Triton X - 100.as an extraction medium. The complex was surrounded by surfactant micelles. The surfactant - rich phase was diluted with methanol and the complex was measured spectrophotometrically at it's (max= 294nm). Different factors that can influence the extraction efficiency of copper ion has been optimized by using one - factor - at - a - time (OFAT). These factors include solution pH, reagent and surfactant concentrations, temperature and incubation time. Besides the interference effect of cations was also considered under the optimized conditions, “preconcentration factor” of 90 was achieved. The linear range was (0.1 - 4)g.mL - 1 with “limit of detection” and limit of quantification (0.0071), (0.0215)g.mL - 1 respectively and molar absorptivity of (19621.5) L. mol - 1. cm - 1.The Stoichiometric study was determined by “mole ratio method and continuous variation method” (Job's) at specific pH. The results showed that the Stoichiometric ratio between copper ion and methionine was 1 : 2.The proposed method is compared with the direct spectrophotometry determination of copper ion and the results have shown that there is a significant differences in accuracy and precision between the two methods and the cloud point extraction which indicates that the latter is more accurate and more precise. The suggested method was applied successfully for the determination of copper ion in water samples

تحضير مشتقات جديدة للفينوكسثين Synthesis of New Phenoxathiin Derivatives

اسم المؤلف: اياد احمد محمد
اسم المشرف: سعاد مصطفى الاعرجي
الموضوع العام: علوم الكيمياء
السنة: 2008
الموضوع الدقيق: الكيمياء العضوية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: تضمن البحث تحضير اربعين مشتقا" جديدا" من مشتقات الفينوكسثين التي تحتوي على حلقات غير متجانسة . وقد تم تشخيصها جميعا" بالطرائق الطيفية : طيف الاشعه تحت الحمراء ( ( FT - IR وطيف الاشعه فوق البنفسجية ( ( UV وطيف الرنين النووي المغناطيسي( 1H - NMR ) لعشرة مركبات وهي [ 1] , [ 2 ] , [ 3e] ,[ [ 3h , [ 4a] , [ 4g ] , [ 5a] , [ 5d] , [ 6e] , [ 6j] , بالاضافة الى تعيين بعض الخصائص الفيزياوية مثل درجة الانصهار واللون . وقد صنفت جميع هذه المركبات المحضرة الى اربعة مجاميع تحتوي كلا" منها على عشرة مركبات .المجموعة الاولى : وهي مشتقات لــ 2 - ( اوكسي الكين - 1 - يل ) الفينوكسثين [ 3a - 3j] والمحضرة من تفاعل 2 - اسيتيل فينوكسثين مع مختلف المركبات العطرية الالدهايدية وبوجود هيدروكسيد الصوديوم . اما المجاميع الثلاثة الاخرى فقد تم تحضيرها من تفاعل مركبات المجموعة الاولى مع كلا" من : 1 - الهيدرازين بوجود حامض الخليك للحصول على مشتقات 2 - ( 1 - اسيتيل بايرازولين - 3 - يل ) للفينوكسثين [ 4a - 4j] .2 - الفنيل هيدرازين بوجود البايبيردين لتعطي مشتقات 2 - ( 1 - فنيل بايرازولين - 3 - يل ) فينوكسثين [ 5a - 5j] .3 - هيدروكـــلوريد الهيدروكسيل امـــين فــــي محـــلول هـــيدروكسيد الصوديـــوم الايــــثانولي لتـــــعطي 2 - ( ايزواوكسازولين - 3 - يل ) فينوكسثين [ 6a - 6j] .جميع مركبات المجامــــيع الثلاثة اعـــــلاه معوضة في الموقــــع ( 5 ) في كلا" مـــن حــــلقات البايرازوليــــن والايزواوكسازولين بمجاميع اريل وحسب المركبات العطرية الالدهايدية المستخدمة في تحضير مركبات المجموعة الاولى . | This work comprises the synthesis of forty new phenoxathiin derivatives containing heterocyclic moieties. All the synthesized compounds were characterized by such spectroscopy means namely FT - IR , ultra violet , and 1H - NMR analysis ( for ten compounds [ 1 ] , [ 2 ] , [ 3e ] , [ 3h ] , [ 4a ] , [ 4g ] , [ 5a ] , [ 5d ] , [ 6e ] , [ 6j ] )with thin layer, melting point and color. These heterocyclic compounds were synthesized in four groups , each one containing ten compounds .The first group is made up of 2 - (oxoalken - 1 - yl ) phenoxathiin derivatives [ 3a - 3j ] obtained from the reaction between 2 - acetylphenoxathiin with different aromatic aldehyde in the presence of sodium hydroxide .The other three groups involve compounds produced from reaction between each compound from the first group with each of : 1 ) Hydrazine hydrate in acetic acid to get 2 - ( 1 - acetylpyrazolin - 3 - yl ) phenoxathiin derivatives [ 4a - 4j ] .2 ) Phenyl hydrazine in presence of piperidine to yield 2 - (1 - phenylpyrazolin - 3 - yl) phenoxathiin derivatives [ 5a - 5j ] . 3 ) Hydroxylamine hydrochloride in ethanolic sodium hydroxide solution to give 2 - (isoxazolin - 3 - yl) phenoxathiin derivatives [ 6a - 6j ] . All these compounds of three groups above are substituted in the position ( 5 ) in both the pyrazoline and isoxazoline rings with different aryl groups according to the aromatic aldehyde used in the preparation of the first group series compounds .

تحضيروتشخيص وقياس قيمة الفعالية البايلوجية لعدد من الايمايدات الحلقية الجديدة المعوضة على ذرة النيتروجين والحاوية على حلقات غير متجانسة Synthesis, Characterization and Evaluation of Biological Activity of Several New N - Substituted Cyclic Imides Containing Heterocycles

اسم المؤلف: احمــد سعــدي حسـن
اسم المشرف: احلام معروف العزاوي
الموضوع العام: علوم الكيمياء
السنة: 2009
الموضوع الدقيق: الكيمياء العضوية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: يهدف بحثنا الى تحضير ايمايدات حلقية معوضة على ذرة النتروجين وحاوية على حلقات غير متجانسة ولغرض تحقيق هذا الهدف تم انجاز الخطوات التالية : 1 - تضمن الجزء الاول تحضير ستراكون ايمايدات معوضة بحلقات غير متجانسة هي مركبات N - (معوض بنزوثايزول - 2 - يل) ستراكون ايمايد [24 - 36] .2 - تضمن الجزءالثاني تحضير N - فنيل ستراكون ايمايدات مرتبطة بحلقة البنزوثايازول عن طريق مجموعة السلفون امايد هي N - (4 - N - معوض بنزوثايازول - 2 - يل) سلفون اميدوفنيل ستراكون ايمايدات [40 - 49].كما تضمن هذا الجزء تحضير N - فنيل ستراكون ايمايدات مرتبطة بحلقات غير متجانسة مختلفة عبر مجموعة السلفون امايد هي N - (4 - (N - مركبات حلقية غير متجانسة) سلفون اميدو فنيل) ستراكون ايمايدات [50 - 53].3 - تضمن الجزءالثالث تحضير N - بنزيل ستراكون ايمايدات مرتبطة بحلقة البنزوثايزول عن طريق مجموعة السلفون امايد هي مركبات N - (4 - (N - معوض بنزوثايزول - 2 - يل) سلفون اميدو بنزيل) ستراكون ايمايدات [57 - 66]. كما تضمن هذا الجزء تحضير N - بنزيل ستراكون ايمايدات معوضة بحلقات غير متجانسة مختلفة عن طريق مجموعة السلفون امايد هي مركبات N - (4 - (N - مركبات حلقية غير متجانسة) سلفون اميدو بنزويل) ستراكون ايمايدات [67 - 70]. 4 - تضمن الجزء الرابع من هذا البحث تحضير ايمايدات حلقية مثل (فثايل ايمايد وسكسن ايمايد) عن طريق جسر استامايدي.وهي المركبات N - (2 - استاميدو (معوض بنزوثايزول - 2 - يل) فثايل ايمايدات [81 - 90]. ومركبات N - (2 - استاميدو معوض بنزوثايزول - 2 - يل) سكسن ايمايدات [91 - 100]. لتحضير الايمايدات المطلوبة تم اتباع الخطوات التالية : ا - تم مفاعلة الامين الاولي الحاوي على حلقات غير متجانسة N - (معوض بنزثايزول - 2 - يل) مع كلوروكلوريد الاستيل لتحويلها الى مركبات 2 - (2 - كلورو استايل امينو) معوض بنزوثايزولات [71 - 80].ب‌ - تم تحويل الفثايل ايمايد والسكسن ايمايد الى املاح البوتاسيوم المقابلة.جـ - تفاعل مشتقات استيل امينو المحضرة في فقرة (ا) مع املاح الفثايل ايمايد والسكسن ايمايد المحضرة في فقرة (ب) لانتاج الفثايل ايمايدات N - (2 - استاميدو - (معوض بنزوثايزول - 2 - يل) فثايل ايمايدات [81 - 90]. والسكسن ايمايدات N - (2 - استاميدو (معوض بنزوثايزول - 2 - يل) سكسن ايمايدات [91 - 100].تم تعيين درجات الانصهار للمركبات المحضرة اجمع في هذا البحث وكما تم تشخيصها طيفيا عن طريق مطيافية الاشعة تحت الحمراء FT - IR وفق البنفسجية U.V. كما استخدمت مطيافية الرنين النووي المغناطيسي 1H - NMR و13C - NMR في تشخيص بعض المركبات المحضرة، فضلا عن اجراء بعض الكشوفات النوعية ذات الفائدة التشخيصية.5 - يتضمن الجزء الخامس الدراسة البايلوجية وذلك للتحري وتقيم الفعالية البايلوجية للمركبات المحضرة ضد انواع من البكتريا والفطريات عزلت كليا من حالات مرضية (بشرية) في مختبرات مستشفى الكاظمية وقد شملت الدراسة على مايلي : ا - دراسة تاثير المركبات المحضرة على نوعين من البكتريا الموجبة لصبغة كرام وهي (ستافلو اوريس وستربتو كوكس بايوجينس). ب - وكذلك على نوعين من البكتريا السالبة لصبغة كرام وهي (سيدومونس واي كولاي). جـ - وقد تم استخدام نوع واحد من الفطريات وهو (كانديدا البكان).وقد اوضحت نتائج الدراسة بان اغلب المركبات المحضرة ذات فعالية بايلوجية | The present work involved synthesis of several N - substituted cyclic imides containing hetero rings.Performing this target includes the following parts : 1 - The first part of this work involved synthesis of several N - substituted Citraconimides containing benzothiazole ring N - (substituted benzothiazole - 2 - yl) Citraconimides [24 - 36]. 2 - The second part involved preparation of N - (phenyl Citraconimides) attached to benzothiazole rings through sulfonamide group (N - (4 - N - substituted benzothiazole - 2 - yl) Sulfonamido phenyl) Citraconimides [40 - 49] and N - phenyl citraconimides attached to hetero cyclic rings through sulfonamide group [50 - 53]. 3 - The third part involved synthesis of N - benzyl citraconimides attached to benzothiazole rings through Sulfonamide group N - (4 - (N - substituted benzothiazole - 2 - yl) Sulfonamido benzyl) citraconimides [57 - 66] and N - Benzylcitraconimide attached to different heterocyclic rings through sulfonamide group [67 - 70]. 4 - This part involved preparation of phthalimides and succinimides attached to benzothiazoles through acetamido group.Producing the desirable phthalimides [81 - 90] and succinimide[91 - 100].All the prepared compounds in this work were characterized by recording their melting points, infrared (FTIR) and ultraviolet (U.V) spectra. H - NMR and C13 - NMR spectra for some of them were recorded also.5 - This part involved evaluation of the biological activity of the prepared compounds against two types of (Gram positive) bacteria including [Staphylococcus aurous and Streptococcusgain] and two types of (Gram negative) bacteria including [E.coli and Pseudomonas aeruginosa].Moreover biological activity of the prepared compounds ast fungi [Candida albicans].were studied also.The results showed that most of the prepared compounds have good biological activity against the mentioned organisms

دراسة التاثير المخفض - المضاد لفرط سكرالدم للمركبات الكيميائية الفعالة المعزولة من النبات الطبي العراقي شوك البحر Study of Hypoglycemic Antihyperglycemic Action of Active Chemical Compounds Isolated from Iraqi Prosopis juliflora Medicinal Plant

اسم المؤلف: جمال حربي حسين السعدي
اسم المشرف: عباس دواس مطر المالكي
الموضوع العام: علوم الكيمياء
السنة: 2015
الدرجة: دكتوراه
اللغة: الانكليزية
مكان الجامعة: البصرة
الصفحات الاولى:
المستخلص: Diabetes mellitus is a disorder in glucose sugar metabolism process becauseof different reasons.leading to a great damage in body systems , therefore medicinalplants were used successfully to treat this disease .The current study was carried outIraqi prosopis juliflora to determine and investigate its hypoglycemic action in bloodof normalglycemic and alloxan induced hypoglycemic rabbits. Many generalextracts were prepared from Iraqi prosopis juliflora pod and leaves ,they are hotaqueous ,cold aqueous ,hot alcoholic ,cold alcoholic ,oils, ethyl acetate and dichloromethane extract .Moreover , some chemical families were isolated from this plantsuch as phenols ,glycosides , flavonoids , tannins ,alkaloids and saponnins.Preliminary qualitative tests were carried out for all prepared extracts thenhypoglycemic and fasted alloxan - induced hyperglycemic rabbits to know activitythese extracts in decreasing blood glucose levels in these rabbits . the resultsindicated that all extracts showed good decreasing in glucose level. Oil extractisolated from prosopis juliflora leaves showed very high activity to decrease blood glucose ,levels in normalglycemic and hyperglycemic rabbits ,where significant decreasing (P<0.05) was found at second and forth hrs , significant decreasing (P<0.01) at sixth hr. and high significant decreasing (P<0.001) at twenty forth hrs. ,whereas leaves glycosides has a great ability to decrease glucose levels in normalglycemic rabbits where a significant decreasing (P<0.01) was found at second and forth hrs., and a high significant decreasing (P<0.001) at twenty forth hrs., but in hyperglycemic abbits , a high activity was recorded and led to a significant decreasing ( P<0.01) at second forth hrs., and high significant lowering( P<0.001 ) at twenty forth .whereas ,leaves tannins extract was noticed to be the lowest affiecieney in reducing blood glucose levels ere it led to a significant lowering ( P<0.01) at twenty forth in normalglycemic rabbits , while a significant decreasing (P<0.05) was recorded at twenty forth in hyperglycaemic rabbits. Leaves ,4 - (2’ - Hydroxyethyl)phenol, Trans - phytol , 24 - Methylencycloartan - 3 - one β - hydroxylup - 20(29) - en 4 - (β - D - Glucopyranosyloxy)benzyl alcohol and Sti masterin (.Were isolated ,separated ,purified and identified by thin layer chromatography, column chromatography, gas chromatography, IR - spectroscopy ,1H,C13 - NMR ,Gas chromatography - mass spectroscopy .Also study of hypoglycemic action of four these chemical compounds isolated from leaves and pods p.juliflora , the glycosidic compound 4 - (β - D - Glucopyranosyloxy)benzyl alcohol recorded strong activity as hyperglycemic action and led to a significant decreasing ( P<0.05) at second hrs., and significant lowering( P<0.01)at fourth ,sixth hrs. and high significant decline (P<0.001) at 24 hrs in normalglycemic rabbits ,while in hyperglycemic rabbits a significant decreasing (P<0.05) at second hrs. ,significant lowering P<0.01 at fourth and sixth hrs and significant decreasing (P<0.001) at twenty forth hrs. The active compound 4 - (2 - - Hydroxyethyl)phenol showed a high hypoglycemic action were significant decline ( P<0.05) at second hrs, a significant decreasing ( P<0.01) at sixth and a high significant decreasing (P<0.001) at twenty forth hrs. in normalglycaemic rabbits ,while in hyperglycemic rabbits , a significant decline (P<0.05) was at second , a significant decreasing (P<0.01) at fourth and sixth hrs., and a high significant decreasing ( P<0.001) was recorded at twenty forth hrs..Also active compound24 - Methylencycloartan - 3 - one showed a significant decrease (P<0.05) at second hrs. , significant decrease (P<0.01) at fourth and sixth hrs., and a high significant decreasing ( P<0.001) at twenty forth hrs hyperglycaemic rabbits, while the compound α - tocopherol recorded a significant decreasing (P<0.05) at sixth hrs. , significant decrease (P<0.01) at twenty forth hrs. in hyperglycemic rabbits. The toxicity for some extracts and active chemical compounds isolated from leaves and pods was studied where no hemolytic for red blood cells was found .

تحضير ايمايدات حلقية ثنائية وبعض مشتقاتها الكبريتية ودراسة خواصها الطيفية والتركيبية , عمليا ونظريا باستخدام نظرية دالية الكثافة IR, NMR, MS Spectra and Structure of Some prepared Bicyclic Imides and Their Thione Derivatives; Experimental and Density Functional Theory studies

اسم المؤلف: عادل امعلا ضمد ال ازيرج
اسم المشرف: ناجي علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: دكتوراه
اللغة: الانكليزية
مكان الجامعة: البصرة
الصفحات الاولى:
المستخلص: The present work involved four parts : First step concerned with the preparation some N, N’ - alkyl (aryl) bismaleimic acidsvia reaction of twice molar amounts of maleic anhydride and hydrazine for compound(A1), and different alkyl and aryl - diamines for compounds A2 - A7. The reaction wascarried out via nucleophilic attack of amino group in maleic anhydride. The structureof the compound (2Z,2Z’) - 4,4’ - (ethane - 1,2 - diylbis (azanediyl)) bis (4 - oxobut - 2 - enoicacid) (A2) was also unambiguously confirmed by X - ray single crystal structureanalysis. The white crystal crystallizes in the monoclinic system, space group C2/cwith the cell dimensions a =7.108(3), b=7.370(2), c= 20.859(6) Å, β = 91.260(4)oand Volume = 1092.65(6) Å3.Molecule is stabilized by an intramolecular O—H…O hydrogen bond. In thecrystal, molecules are connected through intermolecular N—H…O hydrogen bonds.Intermolecular and intramolecular hydrogen bonds coexist to stabilize the structure.The geometry calculated of compounds A1 - A7 was optimized using a Densityfunctional theory DFT with B3LYP hybrid functional and 6 - 311G (d, p) basis set, andis in good agreement with the structure obtained by the X - ray single crystal structureof compound A2. Also the fundamental vibrational frequencies of vibrational bandswere evaluated.The second part of this study was the treatment of N,N - alkyl and (aryl)bismaleimic acid (A1 - A7) with suitable dehydrating agents lead to dehydration andcyclization producing the corresponding N,N - alkyl and (aryl) bismaleimide (AD1 - AD7).The structure of the compound 1,1’ - (sulfonylbis(4,1 - phenylene)) bis (1H - pyrrole - 2,5 - dithione) (AD7) was also unambiguously confirmed by X - ray single crystalstructure analysis. The colorless crystal crystallizes in the monoclinic system, spaceAbstractix0200040000CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2phenyl4,4' - sulfonyldianilinedirect Aliphatic AromaticWavenumber cm¯¹Types of RCH str.CH2 - N strC=O strC - Ngroup P21/c with the cell dimension a =11.698(3), b=15.002(3), c= 20.053(6)Å andβ = 98.818(2)o Volume = 3478.07(13) Å3.FT - IR spectra show the position of the absorption bands vary with the type andlength of the link spacer (R) between the two maleimide rings on the compoundsAD1 - AD7.The absorption frequency of vinyl group increases with increasing methylene aliphatic chain spacer link between two maleimides ring, the correlation between some absorption bands and the type (direct link or aliphatic or aromatic) and length of aliphatic chain link spacer (R) between the two maleimide rings in the studied compounds AD1 - AD7 shown in the chart below.In the third part, a series of new bisthimalemide derivatives were prepared by thionation the compounds AD3, AD6 and AD7 with Lawesson’s reagent LR. Subsequent reaction of bismaleimimides AD3, AD6 and AD7 with Lawesson’s reagent afforded dithio derivatives.

دراسة حيوية كيميائية لتاثير بعض المعادن الثقيلة على حالة الاكسدة مضادات الاكسدة في عمال محطات البنزين في محافظة البصرة العراق Biochemical Study of the Effects of Some Heavy Metals on Oxidant / Antioxidant Status in Gasoline Station Workers /Basra - Iraq

اسم المؤلف: سنان كاظم شنان
الموضوع العام: علوم الكيمياء
السنة: 2013
الدرجة: دكتوراه
اللغة: الانكليزية
مكان الجامعة: البصرة
الصفحات الاولى:
المستخلص: Emission of gasoline and its combustion products are consideredmajor air pollutants with adverse effects on the antioxidant systems in thehuman. The effects of exposure to the vapors of motor gasoline (vehiclesfuel in Basrah), on workers were investigated. The current study included50 workers exposure to gasoline in the gasoline filling stations, ranging inage from 18 to 56 years at a mean of (30.45 ± 9.31), in addition to thecontrol group, which consisted of 50 healthy individuals (non - workingstations filling) ranging in age from 18 to 50 years at a mean of (30.27 ±10.37).The study aims to find a number of biochemical indications and theirrelationship with exposure to gasoline by estimating the activity of the enzyme (δ - aminolaevuIinate dehydratase (ALAD)) which is considered as an indicator of the extent of poisoning by heavy metals, study the activity of enzymatic antioxidant (Glutathione peroxidase (GPx), Superoxide dismutase (SOD), Glutathione reductase (GRx), Glutathione S - transferase (GST), Catalase (CAT)), non - enzymatic antioxidants glutathione reduce glutathione (GSH), study the level of Malondialdehyde (MAD), Total antioxidant capacity (TAC), trace elements (Selenium (Se), Znic (Zn), Copper (Cu), magnesium (Mg)) and heavy metals (lead (pb), mercury (Hg), Cadmium (Cd)) and the results were as follows : 1 - Highly significant decreasing (p <0.001) in workers in the levels of trace elements (Se, Cu, Zn) compared with healthy control, while significantly decreased (p <0.05) in the level of Mg with high significantly increased in the levels of heavy metals (Pb, Hg and Cd) (p <0.001). On the other hand, The results indicated that trace elements (Cu, Mg, Zn, Se) were decreased with increasing of the period of gasoline station workers while for heavy metals (Pb, Hg, Cd) increased were observed.2 - The level of MAD, the end product of lipid peroxidation, was high significantly elevated (P<0.01) contact with a significant decreasing (p <0.05) in the level of TAC in workers when compared with healthy controls. MDA increased with the increase of the period of gasoline station workers. MDA concentrations were increased significantly, indicating the amount of cellular damage. Increase the level of MDA from pollution as the period of pollution, increased might decrease TAC in workers compared with healthy control.3 - Workers group showed a highly significant decrease in the activity of enzymes (SOD, CAT, GPx, GRx, GST, ALAD) and level of GSH (p<0.001) compared with healthy controls. The results showed that increasing the duration of the work in the filling station to produceadecrease in the activity of the enzymes (SOD, CAT, GPx, GRx, GST, ALAD) and level GSH. Also, the current study include the assessment of the impact of heavy metals and MDA on the levels of trace elements (Cu, Mg, Zn, Se), (GSH, TAC) and the activity of the enzymes (SOD, CAT, GPx, GRx, GST, ALAD) through the study of the correlation coefficient (p) and the results were as follows : 1 - The level of MDA showed a highly significant negative correlation with the activity of enzymes SOD (P<0.001) and (GRx, ALAD with p<0.01), a highly significant positive correlation with levels of heavy metals (Pb, Hg, Cd), a significant negative correlation (p<0.05) with levels of (Se, Zn, Mg, GSH) and activity of enzymes (CAT, GRx) and a negative correlation with no significant (P>0.05) with level of Cu and activity of GST in workers.2 - The level of Pb shows a highly significant negative correlation with the levels of trace elements Cu, Zn, Se and activity of enzymes GRx, ALAD (P <0.01), while (p <0.001) with the level of TAC, GSH and activity of enzyme GST, GPx, SOD, a significant negative correlation with level of CAT (P <0.05) and a negatively correlated with no significant with the level of Mg in workers of gasoline stations.3 - The study illustrate also a highly significant negative correlation between Hg level and levels of (Zn, Mg, Cu, TAC) and SOD activity (P < 0.001), while there was a significant negative correlation (P < 0.05) with the level of Se and CAT, GPx, GRx, ALAD activity and a negative correlation, but not significantly with level of GSH and GST activity in serum of gasoline station workers.4 - The level of Cd showed similar behavior of other heavy metals a highly significant inverse correlation with the levels of Se, Cu, TAC and the activity of SOD (p <0.001), a significantly with the level of Zn, GSH and ALAD, CAT, GPx activity (p<0.05), while there was a negative correlation , but not significant (P > 0.05) with levels of Mg and GRx , GST activity in workers.

دراسة تركيز الهبسيدين , حالات الحديد وبعض المتغيرات الكيموحياتية في مرضى متلازمة المبيض متعدد الاكياس

اسم المؤلف: دعاء نعمــــة مســـلم الزامــــــلي
اسم المشرف: هناء عداي علي السلطاني
الموضوع العام: علوم الكيمياء
السنة: 2015
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: النجف
الصفحات الاولى:
المستخلص: تعد متلازمة المبيض متعدد الاكياس ( PCOS ) واحدة من اشهر اضطرابات الغدد الصماء غير المتجانسة والاكثر تعقيدا للنساء في سن الانجاب. عادة ما تكون مرتبطة مع مقاومة الانسولين (IR) المرافق لفرط نسبة الانسولين في الدم كعملية تعويضية. الارتفاع المزمن لهرمون ( LH ) ومقاومة الانسولين هما الاكثر شيوعا لانحرافات الغدد الصماء والتي تضهر في متلازمة المبيض متعدد الاكياس.في الدراسة الحالية فان مستوى هرمون الهيبسيدين وحالات الحديد (Total Iron، Ferritin، TIBC، UIBC، %TS، TF) تم دراستها ومقارنتها مع العديد من العلامات الجسمانية من(العمر، الوزن، الطول، مؤشر كتلة الجسم، ونسبة الورك الى الخصر (WHR) والهرمونات (LH، FSH، TT، FT، SHBG، E2، Progesterone، Prolactin ) ومتغيرات مقاومة الانسولين التي تتضمن (مستوى السكر في حالة الصيامFBG، ونسبة الانسولين في حالة الصيامFIN ومقياس مقاومة الانسولين HOMA - IR) وبعض المتغيرات الكيموحياتية (الدهون الثلاثية، نسبة الكولسترول في الدم ، نسبة الكولسترول الجيد العالي الكثافة والكولسترول الضار الواطئ الكثافة) في مرضى متلازمة المبيض متعدد الاكياس ومجموعة الاصحاء. اضافة الى ذلك تم تقسيم مرضى (PCOS) الى عدة مجاميع طبقا للمعايير التالية : (وجود الشعرانية، وجود انتظام الحيض، وجود العقم الاولي والثانوي، وجود مقاومة الانسولين والحساسية للانسولين بالاعتماد على(HOMA - IR≥3 ) .تم اختيار ستون (60) مريضة مصابة بمرض متلازمة المبيض متعدد الاكياس (PCOS) تتراوح اعمارهم بين (15 - 42) سنة. تم تشخيص مرض (PCOS) من قبل طبيبة نسائية متخصصة في مركز الخصوبة في مستشفى الصدر التعليمي في النجف الاشرف خلال الفترة من (شهر ديسمبر 2014 الى شهر مايو 2015). كذلك اختيرت (30) امراة سليمة تتراوح اعمارهن بين (15 - 42) سنة. تم قياس المتغيرات الكيميائية (نسبة السكر في الدم في حالة الصيام، قياس تركيز TG، الكولسترول، HDL، Total Iron وTIBC باستخدام طرق طيفية. بينما تم قياس تراكيز كل من (نسبة الانسولين في حالة الصيام ، الهيبسيدين، Ferritin، LH، FSH، TT، SHBG وProgesterone، E2 وProlactin)باستخدام طريقة (ELISA). تم حساب مقاومة الانسولين (HOMA - IR) باستخدام المعادلة التالية (تركيز السكر في الدم في حالة الصيام × تركيز الانسولين في الدم في حالة الصيام / 22.5).في الدراسة الحالية وجد ان الزيادة في تركيز الانسولين في حالة الصيام (p=0.001) ، HOMA - IR (p=0.001) ، LH (p=0.001) ، ونسبة LH / FSH (p=0.001) وProgesterone (p=0.001) ، SHBG (p=0.001) ، TT وFT (p=0.001) ، E2 (p=0.001) ، Prolactin (p=0.001) ، الكولسترول ، HDL ، LDL والدهون الثلاثية (p=0.001 ) ، Total Iron ، TIBC ، Ferritin ، TS ٪ ، UIBC وTF (p=0.001) وهرمون الهيبسيدين (p=0.001) عندما قورنت مجموعة متلازمة المبيض متعدد الاكياس مع مجموعة الاصحاء. بينما اضهرت الدراسة الحالية عدم وجود تاثير لنقصان تركيز السكر في حالة الصيام ونسبة هرمون FSH (p>0.05) خلال المقارنة. وجد في الدراسة الحالية ان تغيير مستويات هرمون الهيبسيدين يعتمد بصورة رئيسية على حالات الحديد ومقاومة الانسولين . | Polycystic ovary syndrome (PCOS) is one of the most complex common and heterogeneous endocrine disorders of women in the reproductive age. It is frequently associated with insulin resistance (IR) accompanied by compensatory hyperinsulinaemia. Chronically elevated luteinizing hormone (LH) and insulin resistance are 2 of the most common endocrine aberrations seen in PCOS. In the present study, the level of serum hepcidin and Iron status(total iron, ferritin, TIBC, UIBC, TS%, TS.c) studied and compared with many descriptive (age, weight, height, BMI, hip/waist ratio (WHR) , hormonal (LH, FSH, total testosterone, Free testosterone, SHBG, E2, progesterone, prolactin and insulin resistance parameters including (FBG, fasting insulin, homeostasis model assessment of insulin resistance HOMA - IR) and some biochemical parameters (TG, Cholesterol, HDL, LDL) in PCOS and control groups. Furthermore, PCOS patients are sub grouped according to the following criteria : presence of hirsutism, presence of regularity of menstruation, presence of primary and secondary infertility, presence of insulin resistant and insulin sensitive state according to HOMA - IR≥3. Sixty (60) polycystic ovary syndrome patients (PCOS) of ages range between (15 to 42) year were recruited. PCOS was diagnosed in patient by the gynecologists of the Fertility Center in AL - Sadder Teaching Hospital in Najaf during the period from (December 2014 to may 2015), 30 healthy women of ages range between (15 to 42) year were included as a control group. Fasting blood glucose, TG, cholesterol, HDL, total Iron and TIBC concentrations were measured by spectrophotometric methods. Fasting insulin, hepcidin, ferritin, LH, FSH, total and free testosterone, sex hormone binding globulin, progesterone, E2 and prolactin levels were measured by enzyme linked immune - sorbent assay methods. Insulin resistance was estimated by( HOMA - IR) using the equation (Fasting blood glucose × fasting insulin/22.5) . In the present study Significant increase of the concentrations of fasting insulin (p=0.001) , HOMA - IR (p=0.001) , LH (p=0.001) , LH/FSH ratio (p=0.001) , progesterone (p=0.001) , SHBG (p=0.001) , total testosterone (TT) and free testosterone (FT) (p=0.001), E2 (p=0.001) , prolactin (p=0.001), cholesterol, HDL, LDL and triglycerides(p=0.001) , total Iron, TIBC, ferritin, TS%, UIBC and TF (g/L) (p=0.001) and hepcidin hormone (p=0.001) were obtained in the group of polycystic ovary syndrome patients group when compared with those of the control group. Fasting blood glucose and FSH showed no significance (p>0.05) were noticed during a comparable evaluation. In the present study Changes of Hepcidin levels are dependent directly on Iron status and insulin resistance

التشخيص الكيميائي والفولتامتري للبولي بيوتيلين سكسنيت الملدن بواسطة ايبوكسي (زيت النخيل)

اسم المؤلف: حسن رحيم حمود الدحيدحاوي
اسم المشرف: عماد عباس جعفر هناء عداي علي
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: النجف
الصفحات الاولى:
المستخلص: في هذه الدراسة ، تم استخدم ايبوكسيي زيت النخيل EPO كملدن للبولي بوتيلين سكسينيت باستخدام الكلوروفورم كمذيب ، تم خلط ستة اوزان من PSPE وقد استخدم جهاز FTIR الطيفي لتحديد المجاميع الفعالة . كما وتم قياس الاستقرارية الحرارية والتحلل البيولوجي ، والخصائص المورفولوجية للخليط بواسطة جهاز التحليل الحراري الوزني TGA ، المجهر الالكتروني الماسح SEM وتقنية FTIR ، حيث اظهرت النتائج بان هناك بعض التاثر بين المركبين بوجود الاواصر الهيدروجينية التي تربط بين نهايات المجاميع الفعالة للبوليمر OH وبين حلقة الايبوكسي . مزيج الـ PSPE اظهر استقرار حراري عالي وتحسن في الخواص البيولوجية مقارنة مع الـ PBS النقي . كما اظهرت النتائج المورفولوجية للخليط ان EPO كان ذو قابلية امتزاجية جيدة مع PBS. تم تعديل قطب الكربون الزجاجي GCE مع طبقه رقيقة من (PSEP ) باستخدام طريقة محلول التبخر لانتاج القطب الجديد المعدل . PSEP/GC تم ايضا دراسة عمليات الاكسدة والاختزال لسداسي سيانيد الحديدات (II) باستخدام الـCyclic Voltammetry . وقد تبين ان ذروة الفصل ΔEpa - c ) ) بين قمم الاكسدة لايون فروسيانيد في محلول مائي هو 120 ملي فولت ، ونسبة التيار لقمم الاكسدة، IPA / IPC، كانت 1.6 لـ PSEP / GCE، مؤشرا انعكاسية وقابلية توصيلية جيدة للقطب المعدل. وبالتالي، فانه يمكن استخدامها لتحليل الجهد الكهروكيميائي . الخواص الفيزيائية للقطب المعدل PSEP / GCE تمثلت بالصلابة الجيدة، التصاق العالي على الاسطح المعدنية للقطب الالكتروليت الجامع ، بالاضافة الى الذوبانية والاستقرارية الجيدة للـPSEP على .GCE ايضا، الحساسية في ظل ظروف الـ cyclic voltammetry تعتمد بشكل كبير على تراكيز مختلفة من فروسيانيد ، الالكتروليت المستخدم ومعدل المسح . وقد لوحظ خلال معدلات مسح مختلفة بان قمم الاكسدة والاختزال للحديد / (III) الحديد (II) تمت بعملية معكوسة. | In this study, epoxidized palm oil (EPO) was utilized as a blended for poly butylene succinate (PBS) using chloroform as a solvent by solution casting process at six weight of PSEP. Fourier - transform infrared (FTIR) spectroscopy was used to identify the functional groups of PBS and PSEP blends. Thermal stability, biodegradable, and morphological properties of the blends were investigated by thermo gravimetric analyzer (TGA), and scanning electron microscope (SEM) technique. The FTIR spectra indicate that there are some molecular interactions by intra molecular hydrogen bond between PBS and EPO. All sets of PSEP blends show high thermal stability and significant improvement of biodegradable properties compared to pure PBS. Morphological results of PSEP blends show that EPO was good miscible with PBS. Aglassy carbon electrode (GCE) was modified with a poly butylene succinate - epoxidized palm oil (PSEP) film using a solution evaporation method to produce a new modified electrode PSEP/GCE. The redox process of K4[Fe(CN)6] during cyclic voltammetry was studied using the PSEP/GCE. It was found that the peak separation (∆Epa - c) between the redox peaks of ferrous cyanide ion in an aqueous solution is 120 mV and the current ratio of redox peaks, (Ipa/Ipc), is 1.6 for the PSEP /GCE, indicating good reversibility with good conductivity of the modified electrode. Hence, it can be used for voltammetric analysis. The physical properties of the modified electrode PSEP/GCE include good hardness, high adhesion to the metal surfaces of electrode collectors, solubility and good stability of the PSEP on GCE. Also, the sensitivity under conditions of cyclic voltammetry is significantly dependent on different concentrations of ferrous cyanide , the electrolyte used and the scan rate. At different scan rates, oxidation - reduction peaks of Fe(III)/Fe(II) were observed in a reversible process

تقدير البروتينات الدهنية والاجهاد التاكسدي في مصل المصابين بمرض حب الشباب Evaluation of Serum Lipid Profile and Malondialdehyde in Patients with Acne

اسم المؤلف: رنا عبد العالي الرفيعي
الموضوع العام: علوم الكيمياء
السنة: 2008
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: النجف
الصفحات الاولى:
المستخلص: The present study was conducted to verify the relevance of lipids and lipoproteins levels and their byproduct of oxidation, malondialdehyde (MDA) in acne patients. The design of the project included one hundred acne patients (47% males and 53% females)and 40 apparently healthy individuals (control group). Total serum cholesterol (TC), high density lipoprotein cholesterol (HDL - C), triglycerides (TG), low density lipoprotein (LDL - C), very low density lipoprotein (VLDL - C) and MDA levels were measured in acne patients and the control group.The results indicated significant (P≤0.05) elevations for TC, TG, LDL - C, VLDL - C and MDA levels in acne patients with respect to those of the control group. Sex differences were obtained as rises forTC, LDL - C and MDA (P≤0.05) in males when compared with thoseof the females. The linear regression analysis exhibited significantpositive correlation for TC (r = 0.68, P≤0.05) and LDL - C (r = 0.48, P≤0.05) with ages of the control group but not in the acne patients.Smoker acne patients demonstrated significant elevations for TC, TG, VLDL - C, LDL - C and MDA (P≤0.05) in comparison with those of the control group, while nonsmokers acne patients showed significant elevations for TC and LDL - C (P≤0.05) during a comparable evaluation. Married acne patients indicated significant increases for TC, TG, VLDL - C, LDL - C and MDA (P≤0.05) when compared with those of the control group, while non married acne patients illustrated significant elevations for TG, VLDL - C, LDL - C and MDA (P≤0.05). The influence of treatment was studied, the data stated significant elevation for TG and LDL (P≤0.05), in treated acne patients when compared with those of the control group, while untreated acne patients showed significant increases for TC, TG, VLDL - C, LDL - C and MDA (P≤0.05) in comparison with those of the control group.These results suggested that oxidative stress is involved in the pathogenesis of acne. We believed that this study is the first to deal with changes of serum lipid profile and oxidative stress in acne patients.

تحويـر المواصفات الريولوجيـة للاسفلـت بالمعالجـة مـع البولـي ستايريـن Modification of Rheological Properties of Asphalt by Treatment with Polystyrene

اسم المؤلف: ايمان اسماعيـل احمـد
اسم المشرف: عماد عبد القادر فائق صالح الدبوني
الموضوع العام: علوم الكيمياء
السنة: 2005
الموضوع الدقيق: الكيمياء الصناعية
الدرجة: دكتوراه
الجامعة: جامعة الموصل
اللغة: الانكليزية
مكان الجامعة: الموصل
الصفحات الاولى:
المستخلص: اكتسبت المواد الاسفلتية المحورة بالبوليمرات اهمية خاصة خلال السنوات الاخيرة وذلك لارتباطها الوثيق بالمجالات الانشائية والصناعية فضلا عن التغيرات الكبيرة الحاصلة في السلوك الريولوجي للمواد الاسفلتية عند اضافة كميات صغيرة من البوليمر.ونظرا لمحدودية عدد الدراسات حول استخدام البولي ستايرين لتحوير الاسفلت جاءت دراستنا هذه محاولة لتوضيح كيفية تصرف البولي ستايرين مع الاسفلت خصوصا اذا علمنا ما تتمتع به مادة البولي ستايرين من مميزات كونها واحدة من اكثر البوليمرات الثرموبلاستيكية شائعة الاستعمال ورخيصة الثمن بالاضافة الى حجم المشاكل البيئية الناجمة عن تراكم كميات كبيرة من هذه المادة كفضلات.اشتملت هذه الدراسة على : 1 - معالجة كل من اسفلت بيجي المشتق من نفط بارافيني الاساس واسفلت قيارة المشتق من نفط اروماتي الاساس بنسب مختلفة من البولي ستايرين معالجة اذابة فيزيائية، بالاضافة الى المعالجة الكيميائية لاسفلت بيجي مع البولي ستايرين.2 - معالجة اسفلت بيجي بنسب مختلفة من البولي ستايرين المكسر حراريا ، معالجة اذابة فيزيائية ، ومعالجة كيميائية ، وملاحظة تاثير تقليل الوزن الجزيئي للبوليمر على تجانسية الاسفلت.3 - تحضير انظمة اسفلتية بالمعالجة الكيميائية المحفزة مع الكبريت لكل من اسفلت بيجي والقيارة ومن ثم اجراء عمليات التحوير بالبولي ستايرين والهدف دراسة مقدار التمازج Compatibility بين البولي ستايرين والانظمة الاسفلتية المحضرة.4 - اضافة الكبريت بنسبه المختلفة (5%،10%،15%) وزنا الى النماذج المستحصل عليها من المعالجات سابقة الذكر بهدف زيادة قابلية الاذابة للبولي ستايرين في الانظمة الاسفلتية ودراسة المورفولوجي Morphology باستخدام المجهر لملاحظة كيفية توزيع وانتشار البوليمر خلال الاسفلت.5 - تجزئة كل من اسفلت بيجي والقيارة الى مكوناته الاساسية (اسفلتين،راتنجات صلبة،راتنجات لينة) ومعالجة كل مكون من هذه المكونات معالجة كيميائية محفزة مع الكبريت ومن ثم تحويرها بالبولي ستايرين ، ثم يعقبها اضافة الكبريت كل ذلك من اجل ملاحظة اي من هذه المكونات اكثر تمازجا مع البولي ستايرين وتاثرا باضافة الكبريت.وباجراء الدراسات المشار اليها اعلاه وجدنا : * قابلية امتزاج البولي ستايرين بالاسفلت تكون محدودة.* ان خفض الوزن الجزيئي للبولي ستايرين اسهم في زيادة تذاوبه مع الاسفلت الذي ادى بدوره الى الحصول على نماذج اكثر تجانسا.* الانظمة الاسفلتية المحضرة بالمعالجة الكيميائية المحفزة مع الكبريت لكل من اسفلت بيجي والقيارة كانت افضل تمازجا مع البولي ستايرين من الاسفلت غير المعالج كيميائيا.* اضافة الكبريت بنسبه المختلفة (5%،10%،15%) وزنا الى الانظمة الاسفلتية المحورة بالبولي ستايرين وبغض النظر عن طبيعتها ادت الى تحسن تجانسيتها بشكل ملحوظ من خلال زيادة انتشار واذابة البولي ستايرين خلال الانظمة الاسفلتية.* عملية تجزئة كل من اسفلت بيجي والقيارة الى مكوناته الاساسية وتحوير كل من هذه المكونات بالبولي ستايرين ثم بالكبريت اثبتت ان المكون الاكثر ارومية هو الاكثر تمازجا مع البولي ستايرين والاكثر تاثرا باضافة الكبريت ، وهذا ساعدنا في اعطاء تفسير للنتائج التي حصلنا عليها. | Polymer modified asphalts (PMA) became of great interest over the last years, because they are closely related to industrial and constructional fields, as the addition of small amounts of polymer dramatically changes the rheological properties of asphalts. Due to the shortage of studies on polystyrene modified asphalts,the present study is a trial to clarify the behaviour of polystyrene with asphalt.Polystyrene was choosen to modify asphalts due to its properties as a cheap and commonly used thermoplastic polymer,as well as the environ mental problems caused by the huge quantities of its residue.The study includes : - 1 - Treating Beji parafenic asphalt & Qiayarah aromatic asphalt with various percentages of polystyrene as well as chemical reaction between polystyrene and Beji asphalt.2 - Physical & chemical treatment of Beji asphalt with various percentages of thermally cracked polystyrene to establish the effect of molecular weight on the compatibility of polystyrene with asphalts.3 - A preliminary modification of asphalt by a catalyzed chemical reaction with sulphur then the compatibility of these systems with polystyrene were studied.4 - Adding sulphur of different weight percentages (5% , 10% , 15%) to the samples produced by the above mentioned treatments in order to increase the capability of polystyrene to solvate in the asphaltic systems and to study the morphology microscopically to notice the dispersion of polystyrene in asphalt.5 - Fractionating Beji & Qiayarah asphalts into their basic components (asphaltene,hard resins,soft resins) and treating each of these components with sulphur by stimulating chemical treatment. Then ,modified with polystyrene in order to notice which one of these components is the most compatible with polystyrene and the most affected by the addition of sulphur.After conducting the above mentioned studies, it was found that : - * The compatibility of polystyrene in asphalt is limited.* compatibility was increased by decreasing molecular weight of polystyrene.* Better compatibility of polystyrene was obtained with STA.* Adding sulphur with weight percentages (5% , 10% , 15%) to the polystyrene modified asphalt led to increase its homogeneity significantly.* Fractionating of Beji & Qiayarah asphalts into its basic components and modifying these components by polystyrene and then by sulphur proved that the most aromatic component is the most compatible with polystyrene and the most affected component by sulphur in a way that helped in justifying the results of the study.

تحضير عوامل مساعدة من بعض اكاسيد الفلزات وتطبيقاتها في الاكسدة الحرارية والضوئية Preparationof Catalysts From Several Metals Oxides and their Application in Thermal and PhotoOxidation

اسم المؤلف: فاطمة علاوي عبد السجاد
اسم المشرف: موسى عمران كاظم
الموضوع العام: علوم الكيمياء
السنة: 2012
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: النجف
الصفحات الاولى:

دراسة الاطياف الاهتزازية والفعالية البايولوجية لبعض القلويدات A study of the vibrational spectra and the biological activity of some alkaloids

اسم المؤلف: ايمان عبد الوهاب عبد الله الكويتي
اسم المشرف: عبد الرزاق عبد الجليل العيسى حسين عبد الكاظم عبد الحسين
الموضوع العام: علوم الكيمياء
السنة: 2008
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: النجف
الصفحات الاولى:
المستخلص: The present study was conducted to extracts several alkaloids and their potency on the contraction of smooth’s Rat intestine .to achieve these aims : (Okra, Potato, Cilca ,Pomegranate, Sweet melon, Water melon, Eggplant , pumpkin , Quince , Oaks, Apple, Broad been ,Cauliflower ,Cinnamon ,spinach) were subjected to extraction by petroleum ether and ethanol.HPLC and Mayer’s test revealed significant amounts of pelletierin from punica granatum,lupanine from spinacia oleracea,sinaxalen from brassica oleracea,jasmonoyl tyrosine alkaloid from vica faba ,solanidine from solanum tuberosum and solanine from solanum melongena,in the enrolled plants.The amounts of these alkaloids were (0.22,0.015,0.043,0.036,0.041,0.031) mg/g Respectively .The interaction of alkaloids (0.1) g/L and the contraction of smooth muscle in rat was examined by IR spectroscopy. with the data exhibited stretching band of (C - N) bond in the rang of (1215 - 1020),as described in the literatures .The wave number of the stretching bands of (C - N)in alkaloids were found to be inversely proportional with the molecular weight of alkaloids .Alkaloids were found to elicit Rat intestinal strain according to the order Pelletierine>Lupanine>Sinaxalen>Jasmonoyltyrosine> Solanidine>Solanine.These results suggest the involvement of (C - N) bonds in alkaloids during the induction of smooth muscle contraction.

دراسة العوامل الكيميوحيوية والتنميط الجيني للانزيم المحول للانجيوسين لدى مرضى اعتلال الكلية السكري النوع 2 Biochemical Study and Angiotensin converting enzyme polymorphism of Nephropathy in T2DM Patients

اسم المؤلف: زينب عباس جواد الطالبي
اسم المشرف: حيدر كامل زيدان السعدي محمود حسين هدوان
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: Diabetes is characterized by high levels of blood - glucose resulting from defect insulin hormone secretion or insulin action, or both of them. Chronic high blood - sugar lead to development and failure in many organs in the body such as heart, blood vessels of the eyes, nerves system and kidneys.The Study evaluation of Angiotensin Converting Enzyme - 1 and Angiotensinogen in Type 2 Diabetic patients according to the following steps : it is directed to evaluate Biochemical parameters in type 2 diabetic patients. Measure the levels of some hormones and some parameters. Study the relationships between these hormones and the Biochemical parameters. The association of Angiotensin converting enzyme gene in some hormonal and physiological parameters in type 2 diabetic Iraqi patients. Determined by Polymerase Chain Reaction (PCR). while the hormones including (Insulin and Erythropoietin) and the physiological parameters (insulin resistance, insulin sensitivity, Fasting Blood Glucose; HbA1C; microalbuminuria; systolic and diastolic blood pressure).This case - control study was done in a period of March 2016 to May 2016, from Al - Sadder Medical City in Al - Najaf center for Diabetes and Endocrine. All blood samples of patients were collected in fasting (8 - 10hr.) Number of patients in Diabetes mellitus (DM) type II. Total patients were (n=66), then divided into three groups according to the duration of the disease, the First subgroup (less than 5 years) (n=22), Second subgroup (5 - 10 years) (n=22) and the last subgroup more than 10 years (n=22). The healthy control includes (n=22) subjects, total numbers becomes (88 persons).VISummaryExcluded from this study : Type I diabetes, Females, smokers Patients, random Patient uncontrolled hypertension, alcoholic patients, types of cancer, Hepatitis and Removal of glands. Both groups were subjected to full history including age, BMI, complete clinical examination such as blood pressure measurement. Laboratory measurements including, fasting blood sugar, HbA1C, Microalbuminuria, Insulin hormone, Erythropoietin hormone, Estimation insulinresistance and sensitivity, Extraction DNA from frozen blood for all control and patients then, determination of ACE I/D genotype were done by using PCR technique.The results show significantly Elevation in Microalbuminuria, HbA1c , Fasting blood - sugar, and insulin resistance in nephropathy diabetic type 2 patients compared with healthy control.ACE - 1 enzyme levels have significant increase and lead to the hypertension in the Diabetic patients. There is no relationship between Erythropoietin hormone level and blood pressure deduce that EPO did not raise blood pressure with the patients according to the results of this study, but caused from Angiotensin converting enzyme - 1. The frequency of DD genotype was 21/44 (50%) in patients type 2 more frequent and significant that was significantly higher than that of patient group ID and II with P value =0.036. while there was no significant in ID genotype between patients in group ID 14/44(31%) with p=0.92 and patient in group II genotype 9/44 (20%) with P value=0.07.This study found that DD genotype of ACE gene may be associated with development of diabetic nephropathy among Iraqi patients and this could lead to the prevention and treatment of this complication (Diabetic nephropathy) in Iraqi diabetic patients.

التقدير الطيفي للنايترازيبام وهيدروكلوريد الكلوربرومازين في بعض المستحضرات الصيدلانية باستخدام تفاعلات لونية جديدة Spectrophotometric Determination of Nitrazepam and Cloropromazine - HCl in some Pharmaceutical Formulations using a new Colorimetric reactions

اسم المؤلف: سارة محمد علي المطيري
اسم المشرف: قاسم حسن كاظم
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: الفصل الاول : تضمن مقدمة عامة عن الادوية والتحاليل الدوائية وبعض المفاهيم الاساسية عن التحليل بالطرق الطيفية المعتمدة على امتصاص الاشعة فوق البنفسجية والمرئية المستعملة في هذا النوع من التحاليل, حيث تضمن البحث على مقدمة عامة عن تفاعلات الازوتة - الاقتران واهميتها في التقدير الطيفي للعديد من المركبات الدوائية, وايضا التفاعلات الخاصة باملاح الدايزونيوم. ومقدمة عن تفاعلات قواعد شف وميكانيكية حدوث هذه التفاعلات, بالاضافة الى تصنيف لقواعد شف حسب المجاميع المانحة. ومقدمه عامة عن دواء النايترازيبام واستعراض للطرق التحليلية المستعملة في تقديره. تضمن البحث ايضا على مقدمة عامة عن تفاعلات الاقتران التاكسدي واهميته في التقدير الطيفي للعديد من المركبات الدوائية واهم العوامل المؤثرة فيها واهم الميكانيكيات المتبعة في هذه التفاعلات. ومقدمة عامة عن مركبات الفينوثايزين وعرضا موجزا لبعض الخواص الكيميائية والاستعمالات الطبية والصيدلانية لمركب الفينوثايزين المدروس هيدروكلوريد الكلوربرومازين (CPZ), واستعراض موجز للطرائق التحليلية المستخدمة في تقدير هذا الدواء.الفصل الثاني : تضمن وصف للاجهزة المستخدمة في الطريقة والمقترحة وكذلك المواد الكيميائية المستخدمة والشركات المصنعة لها, بالاضافة الى طرق تحضير محاليل الادوية والكواشف والحوامض والقواعد والعوامل المؤكسدة والمستحضرات الصيدلانية, بالاضافة الى الطرق القياسية للادوية المستخدمة في الدراسةالفصل الثالث : تضمن وصف طريقتين طيفيتين بسيطة وحساسة لتقدير النايترازيبام في المحلول المائي بعد اختزال مجموعة النايترو (NO2 - ) الموجودة فيه الى مجموعة امين (NH2 - ) باستخدام الزنك وفي الوسط الحامضي, في حالته النقية وفي بعض مستحضراته الصيدلانية, حيث اعتمدت الطريقة الاولى على اقتران النايترازيبام المختزل مع الكاشف العضوي (الثايمول) في الوسط القاعدي, واعطائه صبغة ازو برتقالية مستقرة وذائبة في الماء لها اقصى امتصاص في الطول الموجي (477) نانوميتر. وجد ان الطريقة تتبع قانون بيــر لامبـــرت بمدى تركيز (12 - 0.1) مايكروغرام. مل 1 - , وبمعامل امتصاص مولاري (104×(2.264 لتر.مول1 - .سم1 - , وحساسية ساندل (0.0124) مايكروغرام. سم2 - , وحد كشف (0.02) مايكروغرام. مل1 - , وحد التقدير الكمي (0.072) مايكروغرام. مل 1 - , ومعدل نسبة استرداد (99.52)% , ومعدل الانحراف القياسي النسبي (0.7323)%. اما الطريقة الثانية فاعتمدت على اقتران النايترازيبام المختزل مع الكاشف (بارا - هيدروكسي بنزالدهايد) ليعطي قاعدة شف برتقالية اللون مستقرة وذائبة في الماء لها اقصى امتصاص عند الطول الموجي (484) نانوميتر. وجد ان الطريقة تتبع قانون بيــر لامبـــرت بمدى تركيز (10 - 0.1) مايكروغرام. مل 1 - , وبمعامل امتصاص مولاري (104×(3.14 لتر.مول1 - .سم1 - , وحساسية ساندل (0.0089) مايكروغرام. سم2 - , وحد كشف (0.029) مايكروغرام. مل1 - , وحد التقدير الكمي (0.098) مايكروغرام. مل 1 - , ومعدل نسبة استرداد (99.9)% , ومعدل الانحراف القياسي النسبي (0.579)%. طبقت الطريقتين بنجاح لتقدير النايترازيبام المختزل في المستحضر الصيدلاني والذي كان عبارة عن (حبوب) , اذ وجد ان نتائج الطريقتين تتفق مع المحتوى الاصلي للمستحضرات الصيدلانية ومع نتائج الطريقة القياسية المستعملة في تقدير النايترازيبام, وتم تقييم نتائج الطريقتين المقترحتين من خلال حساب قيم اختباري t وF والتي كانت اقل من القيم الجدولية عند مستوى الثقة 95% مما يدل على ان الطرق المقترحة والطريقة القياسية لا تختلفان بشكل ملحوظ في الدقة والتوافقية. ايضا تضمن الفصل وصف طريقة طيفيه بسيطة وحساسة لتقدير هيدروكلوريد الكلوربرومازين (CPZ) في المحلول المائي بحالته النقية وفي مستحضراته الصيدلانية , تعتمد هذه الطريقة على الاقتران التاكسدي بين الدواء والكاشف العضوي (2,5 - Dimethoxyaniline) واعطاء صبغة زرقاء مستقرة وذائبة في الماء لها اقصى امتصاص عند الطول الموجي (717) نانوميتر. وجد ان الطريقة تتبع قانون بيــر لامبـــرت بمدى تركيز (14 - 0.05) مايكروغرام. مل 1 - , وبمعامل امتصاص مولاري (104×(4.04 لتر.مول1 - .سم1 - , وحساسية ساندل (0.0087) مايكروغرام. سم2 - , وحد كشف (0.024) مايكروغرام. مل1 - , وحد التقدير الكمي (0.082) مايكروغرام. مل 1 - , ومعدل نسبة استرداد (99.94)% , ومعدل الانحراف القياسي النسبي (0.149)%. طبقت الطريقة بنجاح لتقدير هيدروكلوريد الكلوربرومازين في المستحضر الصيدلاني والذي كان عبارة عن (حبوب) , اذ وجد ان نتائج الطريقة تتفق مع المحتوى الاصلي للمستحضرات الصيدلانية ومع نتائج الطريقة القياسية المستعملة في تقدير هيدروكلوريد الكلوربرومازين, وتم تقييم نتائج الطريقة المقترحة من خلال حساب قيم اختباري t وF والتي كانت اقل من القيم الجدولية عند مستوى الثقة 95% مما يدل على ان الطرق المقترحة والطريقة القياسية لا تختلفان بشكل ملحوظ في الدقة والتوافقية. | First chapter includes a general introduction on drugs, pharmaceutical analysis and some basic concepts, based on absorption of ultraviolet and visible light that used in this type of analysis. It had included an introduction to the diazo coupling reaction and its importance in spectrophotometric estimation of many pharmaceutical compounds, as well as the most important factors affecting on the stability. Also include general introduction on Schiff base reactions, the mechanism of this reaction, classification of Schiff base according to the donor groups, general introduction about Nitrazepam (NZP) drug and review of the analytical methods that have been used for the determination of Nitrazepam. Also general introduction about oxidative coupling reaction and its importance in spectrometric determination of many pharmaceutical compounds. Also, the most important mechanisms. General introduction about Chlorpromazine - Hydrochloride (CPZ) drug and review of the analytical methods that have been used for the determination of (CPZ). Second chapter : describes the instruments that have been used in this study, preparation of drugs solutions and their pharmaceutical formulations, also acids, bases and oxidizing agents solutions. And describs the standard methods of these drugs. Third chapter : describes two simple and sensitive methods for the determination of reduced nitrazepam (NZP) in aqueous solution, in its pure state and in pharmaceutical preparations after reducing nitro group ( - NO2) to the amine group ( - NH2) . The first method based on the coupling of reduced (NZP) with organic reagent (Thymol) in alkaline medium to give a stable orange azo - dye soluble in water that has maximum absorption at wavelength (477) nm.Beer's law was obeyed between (0.1 - 12) µg.ml - 1 , a molar absorptivity (2.264 * 104) L.mol - 1.cm - 1 , Sandal's sensitivity (0.0124) µg.ml - 2, the LOD was (0.02) µg.ml - 1 , LOQ was (0.072) µg.ml - 1 , average recovery was 99.52 %, and the average of relative standard deviation was 0.7323 %. The second method depends on coupling of reduced (NZP) with the organic reagent (p - Hydroxybenzaldehyde) to form orange Schiff base soluble in water that has maximum absorption at wavelength (484) nm.Beer's law was obeyed between (0.1 - 10) µg.ml - 1 , a molar absorptivity (3.14 * 104) L.mol - 1.cm - 1 , Sandal's sensitivity (0.0089) µg.ml - 2, the LOD was (0.029) µg.ml - 1 , LOQ was (0.098) µg.ml - 1 , average recovery was 99.9 %, and the average of relative standard deviation was 0.579 %. These two methods were applied successfully for the determination of reduced (NZP) in pharmaceutical formulations (tablets), the analytical results were compared with the claim content of pharmaceuticals and also with the standard method was used for determination of nitrazepam, evaluating the proposed methods results by using F and t - test. It was found results experimental F and t value at 95% confidence level did not exceed the critical values. This means the proposed methods do not differ significally in accuracy and validity with standard method. Also, this chapter described a simple and sensitive spectrophotometric method for determination of chlorpromazine hydrochloride (CPZ) based on oxidative coupling reaction between (CPZ) and the reagent (2,5 - dimethoxyaniline) in the presence of oxidizing agent and acidic medium, to form blue complex soluble in water that has maximum absorption at wavelength (717) nm.Beer's law was obeyed between (0.05 - 14) µg.ml - 1 , a molar absorptivity (4.04 * 104) L.mol - 1.cm - 1 , Sandal's sensitivity (0.0087) µg.ml - 2, the LOD was (0.024) µg.ml - 1 , LOQ was (0.082) µg.ml - 1 , average recovery was 99.94 %, and the average of relative standard deviation was 0.149 %. This method was applied successfully for the determination of (CPZ) in pharmaceutical formulations (tablets and injection), the analytical results were compared with the claimed content of pharmaceuticals and also with the standard method was used for determination of (CPZ), evaluating the proposed method results by using F and t - test. It was found results experimental F and t value at 95% confidence level did not exceed the critical values. This means the proposed method do not differ significally in accuracy and validity with standard method

تحضير وتشخيص المركبات النانوية Nb2O5 /CdS ودراسة الامتزاز وفعالية المحفز الضوئي للايونات الفلزية الانتقالية Synthesis, Characterization of Nb2O5 /CdS Nano Composites, and Study Sorption and Photocatalytic Activity of Transition Metal Ions

اسم المؤلف: زينة طالب عمران
اسم المشرف: ندى يحيى فيروز
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: This study includes preparation of nano composite catalyst Nb2O5\CdS at various ratios by using wet commixing method with changed calcination temperature 200, 500 and 800 ⁰C .The catalysts were characterized using X - rays diffraction (XRD), Fourier Transform Infrared (FTIR), Scanning Electron Microscopy SEM and Atomic Force Microscopy (AFM). Then used all of these ratio that calcinated at various temperature in degradation procedure of both Co (II) and Cu (II) from their aqueous solutions. It was found that the catalyst with a ratio of ( 0.85 : 0.15) and (0.75 : 0.25), which was calcinated at 800⁰C it’s the best ratios for Co(II) and Cu(II). Removal of Co (II) was examined after optimization of removal conditions, for example, mass of catalyst , pH of mixture, effect of temperature ,effect of concentration of Co (II) and effect of addition hydrogen peroxide . The best conditions for this case were pH=4, 0.1 g , 500ppm and temperature equal to30ºC, 0.1M of H2O2. Activation energy was calculated using Arrhenius plot and it was 26.28 kJ/mol.Study adsorption of Co(II) was examined after ideal of conditions for example effect of mass of catalyst , effect of concentration of Co (II), pH of mixture, effect of temperature . The ideal conditions for this case were 0.1 g , 500ppm , temperature equal to30ºC, pH=4, and. Activation energy was calculated using Arrhenius plot and it was 8.363 kJ.mol - 1Kinetics of this procedure was investigated and it was fitted with the pseudo first order kinetics. In addition to that, adsorption isotherms for this process were applied for both Langmuir and Freundlich adsorption isotherms. The obtained results presented that it was agreedIIwith Freundlich adsorption model. Study thermodynamic parameters results exhibited that the negative values of ΔG( - 2.346, - 3.571 , - 4.697 , - 5.259 kJ/mol ) for temperature (15 ,20 ,23 ,30 )oC and the positive ΔH (+55.66kJ/mol) and ΔS (+0.201kJ/mol K) .Removal of Cu (II) was examined after ideal conditions such as mass of catalyst , pH of mixture, effect of temperature , effect of concentration of Cu (II) and effect of addition hydrogen peroxide . The ideal conditions for this case were 0.05 g, 500ppm, 30ºC , pH=3 ,0.1M of H2O2. Activation energy was calculated using Arrhenius plot and it was 9.814 kJ.mol - 1.Study adsorption of Cu (II) was investigated after best of conditions for example effect mass of catalyst , effect of concentration of Co (II),pH of mixture, effect of temperature . The ideal conditions for this case were 0.15 g , 500ppm ,30ºC, and pH=3. Activation energy was calculated using Arrhenius plot and it was 8.866 kJ.mol - 1Kinetics of this process was studied and it was fitted with the pseudo first order kinetics. In addition to that, adsorption isotherms for this procedure were applied for both Langmuir and Freundlich adsorption isotherms. The obtained results presented that it was agreed with Freundlich adsorption model. Study thermodynamic parameters results exhibited that the negative values of ΔG( - 3.110, - 3.919, - 5.785 , - 8.300kJ/mol ) for temperature(15 ,20 ,23 ,30) oC and the positive ΔH (+58.42kJ/mol ) and ΔS (+0.213 kJ/mol K ) .

تصميم وحدة حقن جرياني جديدة لتقدير ايون اليوديد وايون الكرومات Design new flow injection unit for the determination of iodide ion and chromate ion

اسم المؤلف: زهير صالح عبيد الشافعي
اسم المشرف: داخل ناصر طه الزركاني
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: he third chapter contains Several axis's is : The first axis is design FIA unit for determination of chromate ion , and of the work , their components and chosen the Optimum Design .* The second axis included study optimal conditions of system ( effect of flow rate , effect of reaction coil , sample loop , starch loop , calibration curve , reproducibility , dispersion coefficient , sampling rate and dead volume . after fixing the optimum conditions , detection limit ( 5 ppm ) , linearity was over the range of ( 10 ppm - 90 ppm ) and linearity coefficient ( R2 ) was ( 0.999 ) .* The three axis is using the same system in determination iodide ion after change the valve it was best results .* The four axis included study optimum conditions of new system ( effect of flow rate , effect of reaction coil , sample loop , starch loop , calibration curve , reproducibility , dispersion coefficient , sampling rate and dead volume . after fixing the optimum conditions , detection limit ( 3 ppm ) , linearity was over the range of ( 5 ppm - 70 ppm ) and linearity coefficient ( R2 ) was ( 0.9995 ) . also the study calibration curve of chromate in the new system , after fixing the optimum conditions , detection limit ( 3 ppm ) , linearity was over the range of ( 10 ppm - 90 ppm ) and linearity coefficient ( R2 ) was ( 0.998 ) .* The last axis included is study application on the tow system and the difference , system one been applied on aqueous solutions of chromate at ( 50 ppm , 70 ppm ) , system tow been applied on aqueous solution of chromate at ( 50 ppm , 70 ppm ) , Medicine chromium picolinate , aqueous solution of iodide at ( 15 ppm , 25 ppm ) and medicine Boviden iodid 4 %

تحقق نظري لاليات تفاعلات التحلل الضوئي لمركبات الهالوهيدروكربون في طبقة الستراتوسفير Theoretical Investigation of Photolysis Reactions Mechanisms For Halo - Hydrocarbon Compounds In Stratospheric Layer

اسم المؤلف: رؤى عبد الحسين عبد العباس المسعودي
اسم المشرف: عباس عبد علي دريع الصالحي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: تم دراسة الية تفاعل نضوب الاوزون بتاثير ثلاث مركبات من هاليدات الهيدروكاربونات ( 1 - برومو - 1 - كلورو - 1,1 - ثنائي فلوروميثان و1 - كلورو - 2,2,2,1 - رباعي فلوروايثان و1,3 - ثنائي بروموبروبان) نظريا في الطور الغازي. حيث ان دراسة المحاكاة تضمنت مسالك تحلل ضوئي مختلفة. استخدمت مختلف طرائق الكم مثل الحسابات شبه التجريبية والحسابات الاساسية الاولية وحسابات نظرية دالة الكثافة. تم احتساب الفعالية الكيميائية والقيم الطاقية لجميع الاصناف الكيميائية التي شملتها الدراسة بواسطة سطوح جهد الطاقة ومعاملات الاواصر وعزوم ثنائية الاقطاب وطاقات الاوربيتالات الجزيئية وطاقة نقطة الصفر لاستبيان المسلك الاكثر احتمالا لتفاعلات التحلل الضوئي واقتراح ميكانيكية التفاعل. تم تقدير الدوال الثرموديناميكيه (∆S°, ∆G°, ∆H°) وطاقة التنشيط وثابت السرعة والتردد الخيالي مع نقطة الصفر لتقدير الحالة الانتقالية الحقيقية والاصناف الكيميائية الاكثر احتمالا بتفاعلات التحلل الضوئي والتي تشارك بميكانيكية نضوب الاوزون.وجد من خلال هذه الدراسة : - ان فجوة الطاقة بين الصيغ الكيميائية التركيبية للاوزون مساوية الى 33.195 كيلو سعره للمول الواحد مع اقل قيمة من حرارة التكوين للاوزون الزاوي والتي مقدارها 45.2773 كيلو سعره للمول الواحد لذلك ان صيغة الاوزون الزاوي (bent ozone) اكثر استقرارا من صيغة الاوزون الحلقي ويمكن ان تتفاعل مع هاليدات الهايدروكاربونات في توجهات فراغية مختلفة. يحصل تفاعل التحلل الضوئي لمركب بروموكلورو ثنائي فلوروميثان من خلال اصرة C - Br مع طاقة تنشيط مقدارها 46.954كيلو سعره للمول الواحد وانثالبي تفاعل مساوي الى 49.749 كيلو سعره للمول الواحد عند الظروف القياسية. تمت ميكانيكية استنزاف الاوزون بواسطة الجذور الحرة الكلور والبروم وثنائي فلوروميثل مع انثالبي تفاعل مقداره من - 48.99الى - 49.057 كيلو سعره للمول الواحد وثابت سرعه مساوي الى 5.34*1017, 6.914*1021 و7.43*1081 ثانيه - 1 لجذر البروم , الكلور وثنائي فلوروميثل على التوالي. ثلاث مولات من الاوزون استنزفت بواسطة مول واحد من مركب بروموكلورو ثنائي فلوروميثان. استنزاف الاوزون بواسطة 1 - كلورو - 2,2,2,1 - رباعي فلوروايثان يتم من خلال جذر الكلور عند طاقة ضوء مساوية الى 65.636 كيلو سعره للمول الواحد وطول موجي مقداره 407.8643 نانوميتر حيث ان مول واحد يستنزف ست مولات من الاوزون مع انثالبي تفاعل مساوي الى - 252.64 كيلو سعره للمول الواحد وطاقه حرة مقدارها - 291.376 كيلو سعره للمول الواحد.3,1 - ثنائي بروموبروبان يتفكك عند طول موجي مساوي الى 442.571 نانوميتر ليحرر جذر البروم وثلاثي بروموبروبان مع طاقة تنشيط مساوية الى 98.624 كيلو سعره للمول الواحد. الاصناف الفعالة الناتجة تستهلك الاوزون بمسالك تفاعل مختلفة لتعطي جذر الالكوكسي وواوكسيد البروم مع تكوين جزيء الاوكسجين بانثالبي تفاعل كلي مقداره - 157.9 كيلو سعره للمول الواحد. | Reaction mechanism study of ozone depletion has been carried out on three selected compounds of halo - hydrocarbons (1 - bromo - 1 - chloro - 1,1 - diflouromethane, 1 - Chloro - 1,2,2,2 - tetrafluoroethane, and 1,3 - dibromopropane) that’s achieved theoretically in the gas phase. The simulation study involves different photolysis reaction pathways. Different quantum methods such as semiempirical, Ab initio and density functional theory have been used in this study. The chemical reactivity and energetic properties of all chemical species that are involved in this study have been computed by the potential energy surface, bond parameters, dipoles moments, molecular orbital energies and zero point energy to estimate the most probable pathway of photolysis reaction to proposed the reaction mechanism. Thermodynamic functions (∆S°, ∆G°, ∆H°), activation energies, rate constant, the imaginary frequency with zero point energy to estimate the real transition state have been calculated to predict the most probable species through photolysis reactions that are contributing to ozone depletion mechanism. From this study, it is found that the energy gap between cyclic and bent ozone equal to 33.195 kCal mol - 1 and the lowest value of heat of formation of bent ozone which equal to 45.2773 kCal mol - 1 so, the bent ozone more stable than cyclic ozone and react with halo - hydrocarbons species in different orientations. The photolysis reaction of bromochlorodiflouromethane occurs through C - Br bond with an activation energy equal to 46.954 kCal mol - 1 and enthalpy change of reaction equal to 49.749 kCal mol - 1 at STP. The depletion mechanism is completed by bromine, chlorine and diflouromethyl radicals with enthalpy change of reaction fall in the range - (48.99 - 49.057) kCal mol - 1 and rate constant values for the reaction of these radicals with ozone equal to 5.34*1017, 6.914*1021, 7.43*1081 s - 1 for bromine, chlorine and diflouromethyl respectively, to deplete three moles of ozone by one mole of bromochlorodiflouromethane. Ozone depletion by 1 - Chloro - 1,2,2,2 - tetrafluoroethane occurs through chlorine radical at 65.636 kCal mol - 1(407.8643nm) of light energy where one mole of the compound destruct six moles of ozone with enthalpy change of reaction equal to - 252.64 kCal mol - 1, and free energy change equal to - 291.376 kCal mol - 1. 1,3 - dibromopropane breakdown at 442.571 nm of light wavelength to released bromine and 3 - bromopropane radicals with activation energy equal to 98.624 kCal mol - 1. 1,3 - dibromopropane exists in three isomers C2, C1 and C2V was found in this study that the isomer C2 is more stable with total energy being equal to - 26652.031 kCal mol - 1. The resulting reactive species consumed the ozone in different reaction pathways to give alkoxy and BrO radicals with the releasing of oxygen molecule with total enthalpy of reaction equal to - 157.9 kCal mol - 1.

دراسات حركية ثرموديناميكية لانزيم الكلوتاثيون الناقل المنقى جزئيا من مصل دم الانسان مع تاثير بعض ادوية علاج السكري

اسم المؤلف: غفران عبد عمران عبد الرضا محمد الخفاجي
اسم المشرف: عودة مزعل ياسر الزاملي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: This study involved (30) Person healthy (15males & 15 femals) the ages were between (20 - 25) years were obtained on samples of students from the university of Babylon / College of Science in Babel province, Iraq has been selected as control group without chronic disease and without smoking.This study attempt isolate GST enzyme from serum human .The partial purification of glutathione - S - Transferase were done using DEAE - Cellulose ,Then purification steps include precipitation by ammonium sulfate 70%, The specific activity was 0.244 U/mg protein and purification degree 1.07 folds and stepwise of Di ethyl amino ethyl - cellulose chromatography and further purified with DEAE - Cellulose column chromatography. The enzyme was apply on DEAE - Cellulose (1.5×30cm) and flow rate 1ml/min and The specific activity was 0.314 U/mg protein with recovery 55.14% and purification degree 1.50 folds.then the glutathione - S - transferase enzyme purified also from serum human by using pre - packed column affinity chromatography by containing glutathione Sepharose 4% and compare specific activity between two separation ways the activity of GST enzyme result from affinity column were more by using ion exchange column and measured of enzyme activity at 340nm by using CDNB as substrate of GST enzyme .The electrophoresis of the partial from human serum from ion - exchange chromatography and affinity chromatography in polyacrylamide gel was found that it was one protein band by using SDS - PAGE analysis by usingenzyme GST result from ion - exchange chromatography 27.7KD and affinity chromatography found (28KD). This study involved also some kinetic studies of GST , maximum activity for GST enzyme was obtained using 22.463mmol/L of 1 - chloro - 2,4 - dinitrobenzene (CDNB)as substrate ,the enzyme showed maximum activityat 35 and optimum pH at 6.8 and time at 12 minutes in incubation at 35 . Using Lineweaver - Burk plot the maximum velocity (Vmax ) and Michaelis constant Km were (11.12mmol/liter) and Vmax (1.254μmol/min) respectively .The thermodynamic constants of activation , were determined by using Arrhenius plot and found to be (35.906kJ. mol - 1, 31.73kJ.mol - 1, - 1.729 kJ.mol - 1.k ,551.40 kJ.mol - 1.k) respectively .Metformin and Dionial inhibition on the GST activity were found that , this lead to drugs effect on enzyme GST.Where showed result that non comparative inhibitor at metformin and showed that comparative inhibitor at dionial .

الاستخلاص بنقطة الغيمة لتقدير الكلور امفينيكول طيفيا في المستحضرات الصيدلانية CLOUD POINT EXTRACTION FOR THE SPECTROPHOTOMETRIC DETERMINATION OF CHLORAMPHENICOL IN PHARMACEUTICAL PREPARATIONS

اسم المؤلف: ضياء يحيى عزيز الحميدي
اسم المشرف: عباس نور محمد الشريفي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: In this thesis chloramphenicol drug was determined by three methods with spectrophotometric technique.In the first method chloramphenicol was reacted with p - N,NDimethyl - aminobenzaldehyde and form yellow Schiff base product which gave higher absorbance at 436.5 nm. Schiff base reaction occurs between two compounds, one contains amino group and the other contains carbonyl group but chloramphenicol is nitro compound therefore it must convert nitro group in drug to amino group therefore reduction process to nitro group necessary for convert it to amino group.Therefore optimum conditions of reduction process were studied to know exactly the volume of concentrated hydrochloric acid which will give higher absorbance of product. Also amount of zinc, temperature of heating and time from heating during the reduction process were studied. Other optimum conditions of reaction also were studied and Calibration curve constructed and regression equation known (y = 0.0556x + 0.0246), also range of concentration which obeys Beer - Lambert Law was (0.1 - 12)ppm, Molar absorptivity (1.8 * 104 ), Sandell's sensitivity (1.8 * 10 - 2), LOD and LOQ (0.037) and (0.124) respectively. also other studies were performed such as accuracy and precision, Molar ratio method, continues variation method, reaction mechanism, Stability constant of product, Analytical applications and t - test and F - test. The proposed method was successfully in determination of chloramphenicol (CAP) in pharmaceutical preparations with good values of recovery presents (97.6% - 102.5%) and Relative Error E% between ( - 2.351 - 2.562).In the second method, chloramphenicol was reacted with 1,2 - Naphthoquinone - 4 - Sulphonic Acid Sodium Salt in basic medium by condensation reaction and form orange - red product which gave higher absorbance at 489 nm.Optimum conditions of reaction were studied and Calibration curve constructed and regression equation known (y = 0.0577x - 0.0006), also range of concentration which obeys Beer - Lambert Law was (1 - 9)ppm, Molar absorptivity (1.86 * 104), Sandell's sensitive (1.73* 10 - 2), LOD and LOQ (0.068) and (0.207) respectively. Also other studies were performed such accuracy and precision, Molar ratio method ,continues variation method, reaction mechanism, stability constant of product, analytical applications and t - test and F - test. The proposed method was successfully in determination CAP in pharmaceutical preparations with good values of recovery presents (96.149% - 103.307%) and Relative Error E% between ( - 3.851 - 3.307) In the third method, cloud point extraction was applied by extractingthe product used in the second method because there is interaction between the alkaline medium and reagent, this the interaction leads to develop colored reagent and some of radiation absorbed at maximum wavelength of product therefore used cloud point extraction to remove the interference and enhancing sensitivity of method and increasing stability of product.Chloramphenicol was reacted with 1,2 - Naphthoquinone - 4 - Sulphonic Acid Sodium Salt in basic medium by condensation reaction forming orange - red product by using same optimum condition of reaction in the second method then the product was extracted from the solution by using cloud point extraction technique.Optimum conditions of cloud point extraction were studied and Calibration curve was constructed and regression equation known (y = 0.2318x + 0.0639), the range of concentration that obeys Beer - Lambert Law was (0.1 - 6) ppm, Molar absorptivity (7.49 * 104), Sandell's sensitivity (4.31* 10 - 3), LOD and LOQ (0.032) ppm and (0.097)ppm respectively. Also Recovery of solute ( was(99.92), preconcentration factor (fc) (3.33333) and phase volume ratio (Rv) (0.3), also other studies were performed such accuracy and precision, analytical applications and test and F - test. The proposed method was successful in determine chloramphenicol (CAP) in pharmaceutical preparations with good values of recovery percent (96.091% - 101.834%) and Relative Error E% between ( - 3.909 - 1.834).Finally, this thesis presented a proposal for a new way to deal with the data in the analytical methods, which includes the new equations to find a slop and y - intercept of a straight line equation as well as introduced new parameters to determine the best linear correlation between the results, it is average of recovery (Arec), the sum of the absolute values of the relative error (SARE) in concentration computed as well as the average of the absolute values of relative error ( AARE) that gives the best results and more accurate than the usual equation.

البلمرة التكاثفية للبنتااريثريتول مع حامض الفثاليك اللامائي وتحويرة ودراسة خواصة Condensation Polymerization of Pentaerythritol with Phthalic Anhydride and Modification and Study of its Properties

اسم المؤلف: رواء حفظي زعولي
اسم المشرف: محمد ناظم بهجت ناظر نجم عبد الله
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: تضمن البحث تحضير الكوبوليمر المحور بخطوتين : الخطوة الاولى ، تتضمن تحضير بوليمرتكاثفي باستخدام بنتا اريتريتول وانهيدرايد الفثالك وانهيدريد الماليئك بواسطة عملية الاسترة .ان الهيكل التركيبي للبوليمر المشترك المحور الذي حصلنا عليه ، كما يلي : وشخص البوليمر المحضر بواسطة مطيافية FTIR وHNMR الخطوة الثانية ، تتضمن تحضير راتنج ذو قوام شرابي باضافة (1مول،1.5مول ،2 مول) مونومير حامض الاكريلك على التوالي الى البوليمر ، لنحصل على تلاثة انواع من الراتنج .تضمن العمل عدد من الفحوصات مثل ، الانتفاخية في الماء والتولوين والايثانول في درجات حرارية مختلفة ، الانتفاخية في محلولي بفر ذوPH مختلف وخواص قوة الشد. تم حساب معاملات الانتفاخية في الماء والتولوين والايثانول،حيث وجد ان محتوى الماء في الهلام المائي يزداد بزيادة زمن الانتفاخية . كذلك تم دراسة تا ثير درجة الحرارة على الانتفاخية في الماء والتولوين والايثانول عند درجات حرارية مختلفة تتراوح مابين 298 - 318 كلفن . تزداد معاملات الانتفاخية بزيادة درجة الحرارة وكذلك فان الكسر الحجمي للراتنج (2 Ф) تقل بزيادة درجة الحرارة .من خلال اختبارات الشد ، لوحظ ان البوليمر المحضرذو سلوك ميكانيكي لين - ضعيف للراتنج المحتوي على الاكريلك اسد. | In this work, a new modified Co - polymer was prepared by condensation polymerization by using phthalic anhydride, pentaerythritol and maleic anhydride through esterification reaction.The structure of modified co - polymer was : Identification of modified polyester resin by FT - IR, 1H - NMRA preparation of pourable syrup resins by the addition of (1, 1.5 and 2 moles) acrylic acid monomer respectively, to the modified polymer, to give three types of resins.Many tests were carried out, i.e., swelling degree in water, toluene and ethanol at different temperatures, and swelling at two different PH. Also the tensile properties of the prepared polymers have been studded.The swelling parameters in water, ethanol and toluene were calculated. The water content, of hydrogels increased with increasing time of swelling. The effect of temperature on the swelling in water, ethanol and toluene at different temperatures ranging from 298 to 318 K was also studied. The water, ethanol and toluene content have been increased with increasing temperature. While the volume fraction of the resins (Ф2) have been decreased with increasing temperatures. From the tensile tests, it was found that the prepared polymer; have soft - weak behavior.

فصل انزيم اللايبوكسيجينيز من مصل الرجال الاصحاء ومعاملة خارجية للانزيم في مرضى الربو Separation of Lipoxygenase from Sera of Healthy men and in Vitro Treatment of Enzyme in Asthmatic Patients

اسم المؤلف: احمد جياد عباس البرقعاوي
اسم المشرف: عودة مزعل ياسر الزاملي
الموضوع العام: علوم الكيمياء
السنة: 2017
الدرجة: دكتوراه
اللغة: الانكليزية
مكان الجامعة: بابل
الصفحات الاولى:
المستخلص: This study is concerned with asthma. Sixty seven asthmatic male patients were examined and tested , their age ranged from 10 - 65 years and they previously diagnosed as asthmatic patient under the physician supervision in AL - Hilla center of Allergy and Asthma . They have the disease for more than five years. Forty patients were examined during the period between July2015 to October 2015, and twenty seven patients were examined during period between June to August 2016, also the control group consisted of sixty seven healthy males ranged from 10 - 65 years.In this study asthmatic patients were divided into three groups according to medication , the first group consisted of (17) asthmatic patients taking antihistamines such as loratadine , citrizine and allermine , while the second group included (24) asthmatic patients taking montelukast , and the third group included (26) asthmatic patients who were on different drugs other than antihistamines and montelukast such as steroids and beta agonists .Five milliliters of blood were obtained from each patient, serum collected absolutely free from hemolysis stored at - 20 °C until uses for measurement of the concentrations of Glutathione, Malondialdehyde, Catalase, Histamine, Serotonin, Lipoxygenase - 5, Leukotriene A4 Hydrolase, total Immunoglobulin E and specific immunoglobulin E.The results revealed that the mean of IgE level (measured by ELISA system)in serum of asthmatic group was (368.16 ±1.772 ng/ml) versus the control group (138.9±2.515 ng/ml) with a significant difference,)P < 0.001(. Asthmatic patients and patients treated with pharmacological drugs such as montelukast and antihistamines showed high sensitivity to some food, animals, plant, palm pollen, fungal and mite allergen and they showed different values between patients and control. The study showed that there is no association between the increased sensitization to food, animal, plant and fungal allergens with age of patients.The present study showed the relationship of count blood cells (WBC and RBC) in studied groups. In all studied groups, WBC values higher than control group while the RBC values showed little differences among all studied groups.According to levels of some variables (histamine, serotonin, LOX - 5 and LTA4H) in asthmatic patients, the results showed a higher mean value of serotonin in asthmatic patients (0.023± 0.004 ng /ml) compared with control group (0.002± 0.001 ng/ml, p˂0.001) In addition the value of histamine was observed high in asthmatic patients (8.511± 0.410 ng /ml)while the control group was (2.565 ± 0.140 ng/ ml) with a significant difference of the mean value of histamine between asthmatic patients and control group (p˂0.001). LOX - 5 level in serum of asthmatic patients was higher (11.080 ± 0. 190 ng/ml) than in control group (9.821 ± 0.203 ng/ml, p˂0.001.The data revealed significant high mean value of LTA4H in asthmatic patients (24.148 ± 0 .450 ng/ml) compared with control group (18.912 ± 0.459 ng/ml, p˂0.001).The result showed that histamine level was increased in the group (>40 years) with a mean value (9.67 ± 4.25 ng /ml ) . While LOX - 5 showed high mean value (11.532 ± 1.274) in the group 20 - 40 years . Also LTA4H enzyme showed high mean value (25.54 ± 3.504 ng/ml)in the group 20 - 40 years , while serotonin appeared with high mean value (0.027± 0.015 ng/ml) in the group (< 20 years) with a significant difference between levels of these variables in each age group (p ˂ 0.001)The mean concentration of an antioxidant, Glutathione(GSH), and Malondialdehyde (MDA) in serum of asthmatic patient and control groups. The mean concentration of MDA increased in asthmatic patients (11.317 ± 1.096 μmol/l) more than control group(8.733 ± 3.756 μmol/l)with a significant difference between these groups (p < 0.05). The mean concentration of GSH increased was in the control (5.106 ± 3.197 μmol/l) more than asthmatic patients(3.905 ± 1.638 μmol/l, p < 0.05).According to the results of the present study, the mean activity of catalase(CAT) was higher (1.555±0.982 U/l) in asthmatic patients when compared with control group(1.173 ± 0.502 U/l, p < 0.05).The current study also concerned with the extrection of lipoxygenase from serum of asthmatic patient and healthy men by taking 15 ml serum from ten asthmatic patients men and 15 ml from serum of ten healthy men. And these quantities of serum were precipitated by ammonium sulfate, The best ratio for precipitating serum and extraction of enzyme is 60%. The anion exchange chromatography was used for extraction of the enzyme. The molecular weight of the extracted enzyme was determined by SDS - PAGE . In this procedure one subunit of the extracted LOXs enzyme showed a molecular weight of 35KD for one chain while a recombinant pure human LOX - 5 showed a molecular weight of 38 KD. The current study used NATIVEN technique for purification of the extracted enzyme obtained from ion exchange chromatography.The results revealed the optimum pH and temperature for LOXs activity and they were 8 and 40°C, respectively.The velocity constant and maximum velocity of the extracted Lipoxygenase enzyme was detected by using PHYWE SYSTEME GMBH SYSTEM, this system had the ability to obtain the relationship between conductivity and concentration (an increase in concentration lead to an increase in conductivity).The extracted lipoxygenase enzyme Km was 2.2mM and Vmax= 140mM/min in asthmatic patients and Km was 2.7mM and Vmax= 135mM/min in controls (by applying Michaelis - Menten equation).While the enzyme Km= 5.5mM and Vmax= 238mM/min in asthmatic patients and Km= 5 mM and Vmax= 208 mM/min in controls (by applying Lineweaver - Burk equation).The extracted LOXs from asthmatic patients and controls was treated with montelukast. The Km and Vmax appeared to have low values Km 3.6mM and Vmax 153mM/min and Km 3.7mM and Vmax 147mM/min, respectively. Also the extracted LOXs from asthmatic patients and controls was treated with molsiodomine, showed low values Km 4.4mM and Vmax 182 mM/min and Km 4.3mM and Vmax 166 mM/min, respectively.

دراسة مستويات بعض مضادات الاكسدة غير الانزيمية وعنصري الحديد والنحاس في مصل دم مرض اضطرابات الغدة الدرقية في محافظة ميسان - العراق

اسم المؤلف: مهدي عودة محمد الساعدي
اسم المشرف: ساهرة غريب صياح
الموضوع العام: علوم الكيمياء
السنة: 2013
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: البصرة
الصفحات الاولى:
المستخلص: the current study was designed to measure some Biochemical function in serum of patients with disorder of the thyroid gland (hyperthyroidism and hypothyroidism ), which can help in the early detection and follow - up of the malfunction of the thyroid gland.Specimens collected from 124 patients with malfunction of the thyroid gland Specimens were classified accord is to the type of disease ( an overactive thyroid gland = 62 , hypothyroidism = 62) and 62 blood samples in were collected from healthy non - infected persons (control group).The study included measuring automatically the levels of thyroid hormones, (FT4, FT3) and (TSH) in the serum using a Mini - VIDAS . The levels of vitamins (E, C) and beta - carotene , and uric acid were measured , also the levels of some trace elements (iron , copper) ,were measured in the serum three above groups.The results showed the following - :  The results of the present study ,the highest percentage of patients with hypothyroidism were indicated that females and the of malfunction of the thyroid gland is occurred at the third and fourth decade of life. The impact of the genetic factor in patients with excessive secretion of the thyroid gland were higher than in patients with deficient secretion of the thyroid gland. A significant increase in the level of the hormone tri - iodothyronin (FT3) and the level of the hormone tetra - iodothyronin (FT4) and a significant decrease in the level of thyroid stimulating hormone (TSH) in patients with excessive thyroid gland secretion compared to the control group. A significant decrease in the level of hormones (FT3), (FT4) and a significant increase in the level of the hormone (TSH) in patients with hypothyroidism compared to the control group.  Generally, there was a significant decrease in the level of vitamins C,E in the sera of patients with malfunction of thyroid compared to the control group. A significant increase in the level of uric acid in patients with excessive thyroid activity and a significant decrease in patients with thyroid failure compared to the control group.  A Significant decrease in the level of beta - carotene in patients with an overactive thyroid , and a significant increase in the level of beta - carotene in patients with hypothyroidism compared to the control group. A Significant decrease in the level of iron in the sera of patients with malfunction compared to the control group. A significant increase in the level of copper in patients with excessive thyroid activity and a significant decrease in patients with thyroid failure compared to the control group.

دراسة التاثيرات الانجابية لبعض العناصر النزرة على العقم عند الرجال في محافظة ذي قار - العراق Reproductive Effects of Some Trace Elements On Male Infertility, In Thi - Qar Governorate/Iraq

اسم المؤلف: ملاك حريز نعيم الخفاجي
اسم المشرف: ساجد حسن كزار ايناس صالح جواد
الموضوع العام: علوم الكيمياء
السنة: 2017
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: ذي قار
الصفحات الاولى:

تحضير وتشخيص وتقيم الفعالية البيولوجية لبعض مركبات الفورمازان المشتقة من قواعد شف الجديدة ومعقداتها مع بعض العناصر الانتقالية Synthesis, characterization and biological evaluation of some new Formazan compounds derived from Schiff Bases and their complexes with some transition Metals.

اسم المؤلف: اعراف محمود داود
اسم المشرف: حيدر عباس مهدي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: ذي قار
الصفحات الاولى:
المستخلص: This thesis contains three chapters represents, the first chapter introduction and interested in studying the chemistry of schiff base and derivatives of formazan, their complexes in terms of their characteristics, importance and synthesis.The second chapter is interested in describing the chemicals and procedures used in the synthesis of the required compounds, and the study of physical measurements, synthesis methods of compounds and evaluation as well as the biological activity.In this research, four new derivatives of formazan (L3, L4, L5 - 4d), which synthesized from the reaction of Diazonium salt amine with suitable Schiff base (L1, L2 - 2d). The Schiff base can product of different primary amines with several aromatic aldehyde and synthesized both of the (Schiff bases, formazans) suitable complexes.The third chapter Results and Discussion, identified synthesized formazan derivatives as well as Schiff bases prefix and its complexes by appropriate spectral methods including of infrared spectroscopy (FT - IR) for all compounds, Nuclear Magnetic Resonance spectrum (1H - NMR) for all compounds Microanalysis (CHNS) for the majority of compounds as well as Mass spectra. For all complexes were recording certain physical properties, such as melting point (m.p.). Monitoring progress of the chemical reaction by using thin chromatography layer (TLC). We synthesis eight complexes (three from Schiff bases and five from formazan derivatives) were complexes with ions (Co, Ni, Cd), then measuring the molar conductivity of complexes. Then study the biological effectiveness for some compounds have been chosen complexes Schiff bases, as well as formazan complexes to determine the effect of active groups in these compounds to evaluate the efficiency ofXIthe compounds against different type of bacteria.The research also includes a test of biological effectiveness of the prepared ligands and their metallic complexes, where we study response inhibitory to the three types of bacteria, a gram positive type of bacteria (Staphylococcus aureuse) and gram negative type of the bacteria (Escherichia Coli and salmonella species) and compared with the standard inhibitor (Cipro).The biological effectiveness swohs positive results as it was noted The ligand L1, L2, L3, L4, L5 and Schiff base 4d Showed lower efficiency than the standard inhibitor trend three types of bacteria. The prepared complexes from ligands appeared high effective than the effectiveness of the ligands itself The formazan (L3, L4, L5 dna 2d) appeared high effective than the effectiveness of the prepared Schiff base

تخليق وتشخيص بعض المركبات الاحادية والثنائية للكاما لاكتام والثايزوليدينون SYNTHESIS AND CHARACTERIZATION OF SOME MONO AND BIS ? - LACTAMS AND THIAZOLIDINONES COMPOUNDS

اسم المؤلف: اصالة سلام جبر
اسم المشرف: محمود شاكر مكطوف التميمي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء العضوية
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: ذي قار
الصفحات الاولى:
المستخلص: This study is concerned with the synthesis and characterization of mono, bis γ - lactams 3(a - h) and mono, bis Thiazolidinone 4(a - i). The structures of the prepared compounds are confirmed by the spectral data include FT - IR spectroscopy , 1H - NMR spectroscopy , 13C - NMR spectroscopy, Mass spectroscopy.Mono and bis γ - Lactams are prepared by reacting Phenyl succinic anhydride with the appropriate Schiff base , in dry chloroform. The obtained mono and bis γ - lactams 3(a - g) is in moderate yields (51 - 75%).The FT - IR spectra showed an absorption bands at (1636 - 1692 cm - 1) attributed to amide carbonyl group ( - N - C=O), and at (1699 - 1733 cm - 1) carboxylic group which attributed (COOH) . The 1H - NMR spectra of compounds 3(a - g),show signals of the aliphatic protons at rang (3.356 - 4.02) ppm and signals for aromatic protons at rang (7.202 - 8.218) ppm. The 13C - NMR spectra of compounds 3(a - e), show signal at rang (171.30 - 178.58) ppm which related amide carbon ( - N - C=O), and at rang (178.32 - 182.16) ppm carboxylic carbon (COOH).Mono and bis Thiazolidinones are prepared by the reaction of thioglycolic acid with Schiff base, in dry benzene. The produced Thiazolidinones 4(a - f) is in moderate yields (55 - 78%).The FT - IR spectra showed an absorption band at (1654 - 1691 cm - 1) attributed to carbonyl group which is related to ( - N - C=O). The 1H - NMR spectra show signals of the aliphatic protons at rang (4.2 - 7.1) ppm and signals for aromatic protons at rang (7.352 - 8.015) ppm. The 13C - NMR spectra show signals at rang (172.32 - 179.52) ppm which is related to amide carbonyl group ( - N - C=O).

دراسة مستويات مصل الهوموسيستين وعلاقته مع بعض انزيمات القلب في المرضى الذين يعانون من احتشاء عضلة القلب في محافظة ذي قار - العراق Study of Serum Homocysteine levels and Its Correlation with Some Cardiac Enzymes in Patients with Myocardial Infarction In Thi - Qar Province/Iraq

اسم المؤلف: اديان سعد حمزة
اسم المشرف: محمد عجة عودة
الموضوع العام: علوم الكيمياء
السنة: 2017
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: ذي قار
الصفحات الاولى:
المستخلص: Myocardial infarction (MI) or acute myocardial infarction (AMI) is the medical term for an event commonly known as heart attack. An MI occurs when blood stops flowing properly to a part of the heart, and the heart muscle is injured because it is not receiving enough oxygen. Biochemical tests are restricted to monitoring cardiac enzymes activities. Therefore, introducing homocysteine test in hospitals for MI patients may provide a clearer picture on the patient condition and help in the disease management.The study was conducted during the period from October 2015 till August 2016. Sixty - three of the people who have a history of injury in the acute myocardial infarction are studied. The diagnosis is based on the clinical presentation and confirmed by ECG, and cardiac enzyme. Forty - eight of persons as healthy volunteers were selected as a control group.The results indicated the following : The proportion of patients male (57%) and females (43%), smokers (49%) and non - smokers (51%), most of them are females. The results also showed that (32%) live in cities, compared to (68%) live in rural areas, and patients Serum homocysteine was significantly higher in MI patients compared to the control group. Homocysteine levels were higher in smokers(p = 0.0001). and unemployed individuals(p < 0.0001)., as well as in individuals with family history of MI or CAD(p < 0.0001). High hypertensive, diabetic and obese individuals had also higher levels of homocysteine . Based on the results of this study suggested measuring the amino acid Homocysteine levels of security as one of the effective ways to diagnose patients with myocardial infarction in hospitals

دراسة كيمو حيوية مقارنه للاجهاد التاكسدي وانماط الدهون في المرضى كبار السن المصابين بمرض الارتجاف الاذني في محافظة ذي قار العراق A Biochemical Comparative Study of Oxidative Stress and Lipid Profile in Elderly Patients With Atrial Fibrillation in Thi - Qar Governorate/Iraq

اسم المؤلف: سارة عاشور ساير
اسم المشرف: رائد معلك حنون الصالح عدنان الطعان الخفاجي
الموضوع العام: علوم الكيمياء
السنة: 2017
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: ذي قار
الصفحات الاولى:
المستخلص: Atrial fibrillation (AF) is the most common cardiac arrhythmia in the general population, and a major cause of morbidity and mortality. Lifetime risk for development of AF has been estimated to 1 in 4 in individuals aged 40 years or more.The present study is designed to determine the levels of oxidative stress by measuring lipid peroxidation product (malondialdehyde MDA), antioxidant state by measuring some antioxidants such as (ceruloplasmin Cp, Transferrin Tf, albumin Alb ,uric acid Ua) ,in addition to lipid profile (cholesterol TC, triglyceride TG, high density lipoprotein cholesterol HDL - C, low density lipoprotein cholesterol LDL - C and very low density lipoprotein cholesterol VLDL - C) in atrial fibrillation patients .The study included (150) subjects; (75) normal subjects (control) and (75) patients with atrial fibrillation. The patients are divided into two groups according to the age : (39) elderly patients [the age range (60 - 80) years] and (36) others patients [the age range (20 - 59) years], also patients are divided in to two groups according to the age with one or more risk factor (Hypertention (HTN), Ischemic Heart Disease(IHD), Heart Hailure (HF)) : elderly which included (18) patients (lone AF) , (21) patients (AF with HTN, IHD, HF) and others which included (17) patients (lone AF), (19) patients (AF with HTN, IHD, HF).The normal subjects (control) also divided into two groups according to the age : elderly [the age range (60 - 80) years] and others [the age range (20 - 59) years] .According to age, the results shown significant increase in the concentration of serum (MDA, Cp, uric acid, TC, TG, VLDL - C, LDL - C ) in elderly and other groups in comparison with their control groups (p≤0.05). It was found significant increase in the concentration of serum MDA in elderly group in comparison with other group, also it was found significant increase in the concentration of serum uric acid in control elderly group in comparison withXIVcontrol other group (p≤0.05). The results also showed non significant differences in the concentration of serum (Cp, uric acid, TC,TG, LDL - C, VLDL - C) between elderly and other groups. It was also found non significant differences in the concentration of serum ( Cp, TC, TG, LDL - C, VLDL - C) between control elderly and control other groups (p≤0.05). While serum Alb , serum Tf and serum HDL - C concentrations show a significant decrease in elderly and other groups in comparison with their control groups (p≤0.05). The results showed significant decrease in the concentration of serum HDL - C in control elderly group in comparison with control other group. Also there were no significant differences in the concentration of serum Alb serum Tf and serum HDL - C between elderly and others groups (p≤0.05).According to the age with one or more risk factor (HTN, IHD, HF) the results show a significant increase in the concentration of serum (MDA, Cp , uric acid, TC, TG, VLDL - C , LDL - C ) in elderly and other groups in comparison with their control groups (p≤0.05). It was found a significant increase in the concentration of serum MDA in the groups AF and AF with HTN, IHD, HF ( in elderly groups) in comparison with groups AF and AF with HTN, IHD, HF (in other groups) respectively (p≤0.05). It was also found a significant increase in the concentration of serum uric acid in control elderly groups in comparison with control other groups , also there were no significant differences in the concentration of serum (CP ,TC , TG ,VLDL - C, LDL - C) between elderly and other groups (p≤0.05). serum Alb ,serum Tf and serum HDL - C show a significant decrease in elderly and other groups in comparison with their control groups, also there was significant decrease in the concentration of serum HDL - C in control elderly groups in comparison with control other groups (p≤0.05). It was also found non significant differences in the concentration of serum Alb and serum Tf between elderly and other groups (p≤0.05).
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