Academic Journal

Development and validation of HPLC and CE methods for simultaneous determination of amlodipine and atorvastatin in the presence of their acidic degradation products in tablets

التفاصيل البيبلوغرافية
العنوان: Development and validation of HPLC and CE methods for simultaneous determination of amlodipine and atorvastatin in the presence of their acidic degradation products in tablets
المؤلفون: Hassan Said A., Elzanfaly Eman S., El-Zeany Salem Badr A., Salem Maissa Y.
المصدر: Acta Pharmaceutica, Vol 66, Iss 4, Pp 479-490 (2016)
بيانات النشر: Sciendo
سنة النشر: 2016
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: atorvastatin, amlodipine, capillary zone electrophoresis, hplc, stability, acidic degradation, Pharmaceutical industry, HD9665-9675
الوصف: Two methods were developed for separation and quantitation of amlodipine (AML) and atorvastatin (ATV) in the presence of their acidic degradation products. The first method was a simple isocratic RP-HPLC method while the second was capillary electrophoresis (CE). Degradation products were obtained by acidic hydrolysis of the two drugs and their structures were elucidated for the first time by IR and MS spectra. Degradation products did not interfere with the determination of either drug and the assays were therefore stability-indicating. The linearity of the proposed methods was established over the ranges 1-50 μg mL-1 for AML and ATV in the HPLC method and in the range of 3-50 and 4-50 μg mL-1 for AML and ATV, respectively, in the CE method. The proposed methods were validated according to ICH guidelines. The methods were successfully applied to estimation of AML and ATV in combined tablets.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1846-9558
Relation: https://doi.org/10.1515/acph-2016-0040; https://doaj.org/toc/1846-9558; https://doaj.org/article/f8f5771aa4d5482585e6722707aa56d2
DOI: 10.1515/acph-2016-0040
الاتاحة: https://doi.org/10.1515/acph-2016-0040
https://doaj.org/article/f8f5771aa4d5482585e6722707aa56d2
رقم الانضمام: edsbas.5FDBF95
قاعدة البيانات: BASE
الوصف
تدمد:18469558
DOI:10.1515/acph-2016-0040