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العنوان
Determination of antimicrobials in dosage forms and biological fluids /
المؤلف
El-Gamal, Rania Mohamed Abdel-Naby.
هيئة الاعداد
باحث / رانيا محمد عبد النبى الجمل
مشرف / فتح الله فتح الله بلال
مشرف / محى خالد شرف الدين
مشرف / منال محمد عيد
الموضوع
Anti-infective agents.
تاريخ النشر
2013.
عدد الصفحات
337 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
Analytical Chemistry
تاريخ الإجازة
01/01/2013
مكان الإجازة
جامعة المنصورة - كلية الصيدلة - Department of Analytical Chemistry
الفهرس
Only 14 pages are availabe for public view

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Abstract

Antimicrobials are among the most commonly used of all drugs. The thesis is devoted to the development of new methods for the analysis of some antimicrobial drugs, namely: ribavirin (RBV), fluconazole (FLZ), tinidazole (TNZ), linezolid (LNZ), rifampicin (RIF) and terbinafine hydrochloride (TRH) in pharmaceutical preparations and/or in biological fluids.This thesis comprises six main parts.The first one included a general introduction about antimicrobials and their lassification.astability-indicating liquid chromatographic method for the determination of ribavirin (RBV) in presence of its degradation products.Two analytical methods including; derivative spectrophotometry and micellar liquid chromatography were developed for the analysis of fluconazole (FLZ) and tinidazole (TNZ) in their co-formulated tablet. The micellar HPLC method was extended to the analysis of the drugs in biological fluids.Micellar HPLC method using monolithic column was developed for the simultaneous determination of linezolid (LNZ) and rifampicin (RIF) in their single dosage forms, this in addition to their simultaneous determination in spiked human plasma and the determination of RIF individually in spiked human urine. A micellar liquid chromatographic method with fluorimetric detection was applied for the determination of terbinafine (TRH) in pharmaceutical formulations and spiked human plasma. A spectrofluorimetric method was developed for the determination of terbinafine HCl (TRH) and linezolid (LNZ) in their pharmaceutical formulations and spiked human plasma. The principles of the proposed procedures as well as the experimental parameters were investigated. Also, the validation criteria of the developed methods were intensively studied. All the results were statistically analyzed and compared with those obtained by official or comparison methods.