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استخدام جسيمات نانوية معدلة لغرض تقدير مركبات البسفينول في نماذج الورق الحراري باستخدام مطيافية الفلورة == Use of modified nanoparticles for the determination of bisphenol compounds in thermal paper samples using fluorescence spectroscopy

اسم المؤلف: احمد سالم كامل
اسم المشرف: بسام فرعون عبد الفرحاني
الموضوع العام: علوم الكيمياء
السنة: 2023
الموضوع الدقيق: الكيمياء التحليلية
الدرجة: ماجستير
اللغة: العربية
مكان الجامعة: القادسية
الكلمات الدلالية:
  • البسفينولات
  • الفلورة
  • الاستخلاص
  • جسيمات النانو
  • الاستخلاص بhplc
  • جسيمات الحديد النانوية
  • بسفينول A
  • بسفينول F
  • بسفينول S
الصفحات الاولى:
المستخلص: تتلخص هذه الرسالة باستعمال الجسيمات النانوية المغناطبسية المعدلة لاستخلاص مركبات البيسفينولBisphenol A(BPA), Bisphenol S(BPS) ,Bisphenol F(BPF) (المواد المسببة لاضطراب الغدد الصماء) من الورق الحراري وكما ياتي : الجزء الاول :تحضير و تعديل الجسيمات المغناطيسية النانوية بواسطة حامض الغاليك لزيادة قابلية تلك الجسيمات على الاستخلاص بكفاءة اعلى وذلك بتحضير متراكب نانوي ثنائي من ( Fe3O4- GA) ثم تشخيصه بتفنية حيود الاشعة السينية والمجهر الالكتروني النافذ والمجهر الالكتروني الماسح حيث وجد ان المركب النانوي يمتلك طبيعة بلورية . الجزء الثاني : تم التحديد والكشف عن حد الكشف والحد الكمي لمركبات البيسفينول BPA, BPS ,BPF)) باستعمال تقنية التحليل الطيفي بالفلورة في درجة حرارة الغرفه وتبين النتائج ان قيم حدود الكشف كانت مقبولة في التحليل الطيفي بتقنية الفلورة المسستخدمة لتقدير هذه المركبات في المحاليل المائية . الجزء الثالث : استخلاص مركبات البيسفينول من الورق الحراري بطريقة النقع باستعمال مذيب مناسب وبدرجة حرارة الغرفة والتاكد من وجود مركبات البيسفينول في المستخلص من خلال قياس شدة التفلور للكشف عنها بطريقة الفلورة واثبتت الطريقه فعالية ممتازة بعد التاكد من وجود تلك المركبات في مستخلص الورق الحراري الجزء الرابع : استعمال الجسيمات النانويه التي تم تحضيرها مسبقا في عملية استخلاص مركبات البسفينول من الورق الحراري حيث بينت النتائج القابلية الكبيرة لهذه الجسيمات النانوية على استخلاص تلك المركبات وبنسب عالية جدا بلغت اكثر من 97%. الجزء الخامس : اجراء دراسات عملية لبعض العوامل المؤثرة على نسب الاستخلاص مثل ( وقت الرج ) ( اختلاف التراكيز ) (عرض الشق بالنسبة لجهاز الفلورة المستخدم) وكذلك تمت دراسة تاثيرواهمية تغليف الجسيمات النانوية في زيادة نسب الاستخلاص من خلال اجراء الاستخلاص بالمركب النانوي Fe3O4 بدون تغليفه ومع التغليف وقياس شدة التفلور الجزء السادس: تم تطبيق تقنية (HPLC) في تحليل مركبات البيسفينول ,BPF , BPS) BPA) في المحاليل المائية القياسية وكذلك مستخلص الاوراق الحراريه . وقد وجد ان التقنية فعالة جدا وقيم حدود الكشف جيدة ومهمة في تقدير هذه المركبات, واضهر مستخلص الورق الحراري وجود نسب عالية جدا من مركب BPS وبدرجة اقل وجود مركب BPA ولم تعطي اشارة على وجود مركب BPF
الملخص:
المصادر:

طرائق جديدة للتحليل بالحقن الجرياني المستمر لتقدير بعض الادوية == New continuous flow injection analysis methods for determination of some drugs

اسم المؤلف: منتظر محمد جبار
اسم المشرف: الهام نغيمش مزعل
الموضوع العام: علوم الكيمياء
السنة: 2023
الموضوع الدقيق: الكيمياء التحليلية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الكلمات الدلالية:
  • UV-Vis spectrophotometry
  • diphenhydramine hydrochloride
  • chlorpheniramine maleate
  • captopril
  • Ayah 6S×1-ST-2D solar cell analyser
المستخلص: This study evaluated captopril (CAP) for arterial hypertension and chlorpheniramine maleate (CPM) and diphenhydramine hydrochloride (DPH) for allergy symptoms. A homemade measuring cell (Ayah 6S×1-ST-2D Solar Cell CFI Analyzer) was utilized to analyze the precipitate from the medications under review. The study compared the new method to UV-Vis spectrophotometric to assess its efficiency, processed the results statistically, and summarized them in order: Part I: Captopril (CAP) was determined by reacting ammonium cerium(IV) sulfate (ACS) with CAP in an acidic medium to form a white, slightly yellowish precipitate, which was measured by reflecting incident light .The Ayah 6S×1-ST-2D solar cell analyzer was used to optimize physical and chemical parameters. The novel approach had a linear range of 0.07-3.0 mmol/L, a correlation coefficient of (0.9983), and a detection limit of 272.5 ng/25 μl. The RSD% was less than 0.2% for n = 8 CAP concentrations of 0.9, 1.5, and 3.0 mmol/L. The approach recovered captopril from three pharmaceutical tablets from various companies with a recovery rate of 97.1039% to 99.8200%. A comparison was done between the new and classical analysis methods. To analyze UV-Vis spectrophotometry at λmax= 207.2 nm, the standard addition method was used with F-test and paired t-test. The two methodologies showed no meaningful difference with 95% confidence in favor of a homemade tool. Part II: Determination of chlorpheniramine maleate (CPM) involved reacting ACS with CPM in an acidic medium to form a white, slightly yellowish precipitate, which was measured by incident light reflecting off the precipitated particles. Some chemical and physical variables were studied and optimized. The linear range was 0.07-5 mmol/L, with a correlation coefficient (r) of 0.9996 and a limit of detection (LOD) of 195 ng/10 μl. The RSD% was less than 0.2% for n = 8 at 1.0, 1.5, and 4.0 mmol/L CPM. The method estimated drug levels in three prescription pills from various businesses with recovery rates of 98.4625% to 99.2400%. A comparison was done between the new approach and the standard addition method for UV-Vis Sp. at λmax = 261 nm using F-test and paired t-test. The two methodologies showed no meaningful difference with 95% confidence in favor of a homemade tool. Part III: DPH Determination The method involved reacting phosphomolypidic acid (PMA) with DPH in aqueous medium to form a white, slightly yellowish precipitate, which was measured by incident light reflecting off the precipitated particles. Some physical and chemical parameters were studied and improved. The linear range was (0.07-9) mmol/L, with a correlation coefficient (r) of 0.9998, and a detection limit (L.O.D.) of 729.55 ng/50µl for the novel approach. The RSD% was less than 0.2% for n = 8 DPH concentrations of 0.1, 4.0, and 10.0 mmol/L. The procedure was successfully applied to three pharmaceutical tablets from various businesses, showing a recovery rate of 97.7437% to 99.7142%. A comparison was made. Compare the new method to UV-Vis Sp. at λmax = 258 nm using the traditional combination method, including F-test and paired t-test. The two methodologies showed no meaningful difference with 95% confidence in favor of a homemade tool.
النص الكامل:
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تقدير بعض المركبات الدوائية باستخدام طر ائق طيفية مختلفة == Determination of some pharmaceutical compounds via different spectrophotometric methods

اسم المؤلف: اوس مسير نجرس خليل الجوعاني
اسم المشرف: معاذ عبد الله نجم الحجار
الموضوع العام: علوم الكيمياء
السنة: 2023
الموضوع الدقيق: الكيمياء التحليلية
الدرجة: دكتوراه
الجامعة: جامعة الموصل
اللغة: العربية
مكان الجامعة: الموصل
الكلمات الدلالية:
  • lisinopril
  • spectrophotometric methods
  • F test
  • t test
  • dopamine
  • mesalazine
  • British Pharmacopeia
الصفحات الاولى:
المستخلص: The thesis included four chapters: Chapter One: It included a general introduction for pharmaceutical compounds (lisinopril dihydrate, mesalazine, and dopamine dihydrochloride), the extent of their importance, their therapeutic role, and the scientific name. It also explained the chemical form and their physical and chemical properties, in addition to the aim of the research. Chapter Two: The second chapter reviewed previous studies on the pharmaceutical compounds under study for four main methods. The standard methods were intended for comparison with the proposed method, in addition to spectroscopic methods, chromatographic methods, and electrochemical methods, which were reviewed according to the chronological order of the studies obtained. Chapter Three: It includes the practical part, which shows the purity of materials and methods of preparing solutions for the chemical compounds used, in addition to showing the place of obtaining pharmaceutical preparations and methods of preparing their solutions for the purpose of study, and the devices used in the preparation, measurement and determination processes. Chapter Four: It included a review of the results obtained from determining the optimal conditions and their application to pharmaceutical preparations and their discussion. The chapter was divided into three parts. The first part included two sides, the first of which reviewed the results of the indirect spectroscopic determination of lisinopril dihydrate by means of bleaching dye reaction resulting from the reaction of lisinopril dihydrate with N. - Bromosuccinimide as an oxidizing agent in an acidic medium, then reacting the excess of the oxidizing agent with the indigo-carmine dye, which works to bleaching dye. All the factors that affected the reaction were studied, namely: the amount and type of acid used to provide the acidic medium, as well as the optimal amount of dye for use. The times required for complete oxidation and the time required for the color of the dye to fade were also studied. After establishing this, the determination range was determined based on Beer’s law, and it was 5-60 µg.ml-1. The value of the Molar absorptivity was 0.18 x 104 L.mol-1.cm-1 and the Sandell's sensitivity was 0.232 µg.cm-2, which indicates that the method has good sensitivity. The average percentage of recovery and the relative standard deviation were 99.75% and 1.527, respectively, which It indicates that the method had good accuracy and precision. The second side, determination of lisinopril was through the relative derivation of the lisinopril pharmaceutical preparation combined with the amlodipine compound, using the fourth derivative spectrum method, and by determining the appropriate wavelengths in estimating the pharmaceutical preparations incorporated into the pharmaceutical preparation at the same time. It gave flexibility in estimating the two compounds simultaneously by providing three longer wavelengths for lisinopril dihydrate (203, 207, 231 nm) and three longer wavelengths for amlodipine (215, 254, 277 nm). Good accuracy and compatibility were available at each wavelength, in addition to being unaffected by the presence of Excipients and additives for the pharmaceutical preparation. The second part refers to the part of the mesalazine drug compound. The first side was based on the determination of mesalazine using the nitration and coupling reactions with DHNP through the formation of the diazonium salt of mesalazine by taking equal concentrations of the mesalazine compound and sodium nitrite (6.530×10-4 mol.L-1) and adding 3 ml of concentrated hydrochloric acid (11.8M) gradually, stirring continuously, and cooling in an ice bath. Then studied the times required to reach a complete reaction of dizonium salt, The value of the Molar absorptivity was 1.58×104 L.mol-1.cm-1 and the Sandell's sensitivity was 0.0082 µg.cm-2. The average percentage of recovery and the relative standard deviation were 99.2% and 0.029 respectively, As for the second side of the determination of the mesalazine compound, it relied on the reaction of complex formation with one of the iron salts, represented by iron(III) sulphate , it gave linearity Between 2.5-30 µg.ml-1, accuracy represented by average recovery which was at 99.33%, and precision represented by the relative standard deviation, which was 3.29, and the Molar absorptivity value and Sandell's sensitivity were solved as follows: 2.78×103 Lmol-1.cm-1 and 0.054 µg.cm-2, which represent sensitivity method. The third part was about the determination of dopamine hydrochloride and was estimated in two ways. The first relied on the oxidation reaction and coupling with 5-amino salicylic acid (mesalazine) as a coupling agent in a basic medium of sodium hydroxide in the presence of sodium persulfate (Na2S2O8) as an oxidizing agent. The method gave good results in terms of extent The estimate was 2.5-31.25 µg.ml-1. With good sensitivity, by finding the value of the Molar absorptivity and Sandell's sensitivity were solved as follows: 0.55×104 l.mol-1.cm-1 and 0.034 µg.cm-2. In addition to the average recovery of 100.93% and the relative standard deviation of 1.13, which represent the accuracy and precision of the method. As for the second method, which relied on indirect determination through a redox reaction, using yttrium ion as an oxidizing agent and 1.10-phenanthroline as a reagent. The reaction was conducted in an acidic medium provided by hydrochloric acid. The method was successfully applied for determination within a linear range between 0.5-10 µg.ml-1 and good sensitivity was determined by calculating the values of the Molar absorptivity and the Sandell's sensitivity which were 1.44 ×104 lmol-1.cm-1 and 0.0131 µg.cm-2, with an average recovery of 99.58% and a relative standard deviation of 0.83, which represent accuracy and precision , which it was good .
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