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العنوان
Analysis of certain cardiovascular drugs in pharmaceutical preparations and biological fluids /
المؤلف
Bakr, Norhane Attaa Mahfouz Mohamed.
هيئة الاعداد
باحث / نورهان عطاء محفوظ محمد بكر
مشرف / منال محمد عيد
مشرف / ياسر الشبراوي السيد
مشرف / سمر سعد السيد
مناقش / ناهد العناني
مناقش / غادة مكاوي حداد
الموضوع
Pharmacy. Drug Toxicity. Cardiovascular Diseases.
تاريخ النشر
2021.
عدد الصفحات
197 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الصيدلة ، علم السموم والصيدلانيات (المتنوعة)
تاريخ الإجازة
1/4/2021
مكان الإجازة
جامعة المنصورة - كلية الصيدلة - قسم الكيمياء التحليلية الصيدلية
الفهرس
Only 14 pages are availabe for public view

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from 191

Abstract

The present thesis is devoted for developing new methods for the analysis of some drugs used for treatment of cardiovascular diseases, namely: either in pure form, in pharmaceutical preparations or in human plasma , namely: Ezetimibe (EZT), atorvastatin calcium (ATR), losartan potassium (LOS), rosuvastatin calcium (ROSU), furosemide (FURO), torsemide (TSM). Different analytical techniques were applied for determination of the studied compounds. The thesis comprises five main parts: Part I: Included a general introduction about cardiovascular diseases drugs, their classification, and their pharmacological actions. Part II: This part involved the development of Simultaneous RP-HPLC method for determination of Ezetimibe and Atorvastatin calcium in pharmaceutical dosage forms and human plasma. Part III: In this part a first derivative synchronous spectrofluorimetric method was developped for estimation of losartan potassium and atorvastatin calcium in pure form and tablets. Part IV: A validated synchronous spectrofluorimetric method was developed for estimation of ezetimibe and rosuvastatin calcium in bulk and pharmaceutical tablets. Part V: In this part two analytical methods including spectrophotometric and spectrofluorimetric methods were developed for determination of furosemide and torsemide in pure form and pharmaceutical formulations using 1, 10 phenanthroline-Fe III reagent.