LC, MS n and LC–MS/MS studies for the characterization of degradation products of amlodipine

Author:

Tiwari Ravi N.,Shah Nishit,Bhalani Vikas,Mahajan Anand

Publisher

Elsevier BV

Subject

Analytical Chemistry,Electrochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Pharmacy

Reference29 articles.

1. ICH, Stability testing of new drug substances and products Q1A(R2), in: Proceedings of the International Conference on Harmonisation, IFPMA, Geneva, 2003.

2. Stability Testing of Active Pharmaceutical Ingredients and Pharmaceutical Products;WHO,2007

3. Development of validated stability-indicating assay methods critical review;Bakshi;J. Pharm. Biomed. Anal.,2002

4. The importance and the challenges of impurity profiling in modern pharmaceutical analysis;Görög;TrAC,2006

5. Application of liquid chromatography-two-dimensional nuclear magnetic resonance spectroscopy using pre-concentration column trapping and liquid chromatography–mass spectrometry for the identification of degradation products in stressed commercial amlodipine maleate tablets

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