Determination and characterization of degradation products of Anastrozole by LC–MS/MS and NMR spectroscopy
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference15 articles.
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3. Isolation and characterization of process related impurities in anastrozole active pharmaceutical ingredient;Hiriyanna;J. Braz. Chem. Soc.,2008
4. LC and LC–MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets;Ramachandra Reddy;J. Pharm. Biomed. Anal.,2009
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1. Mini Review on Forced Degradation Studies on Anti-Epileptic Drugs and Beyond;Journal of Chromatographic Science;2022-08-18
2. Degradation Kinetics Study of Anastrozole in Different Conditions by Reverse-Phase High-Performance Liquid Chromatography and Confirmation of its Major Degradation Product by Ultra-Performance Liquid Chromatography with Tandem Mass Spectrometry;Current Pharmaceutical Analysis;2019-02-11
3. Forced Degradation Studies;Journal of Analytical & Pharmaceutical Research;2016-12-14
4. Understanding unconventional routes to impurities from drugs in hydrolytic conditions;Indian Journal of Pharmaceutical Education and Research;2016-08-01
5. A Review of Chromatographic Methods Used in the Determination of Anastrozole Levels;Indian Journal of Pharmaceutical Sciences;2016
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