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A REVIEW ON METHOD DEVELOPMENT AND VALIDATION OF LC-MS/MS FOR ANALYZING POTENTIAL GENOTOXIC IMPURITIES IN GLIFLOZINS

descriptionPublicationkeyboard_double_arrow_right Article 26 Aug 2023Publisher:Zenodo
Authors: B. Akhila*, B.V. Ramana;

doi: 10.5281/zenodo.8285484 , 10.5281/zenodo.8285485

A REVIEW ON METHOD DEVELOPMENT AND VALIDATION OF LC-MS/MS FOR ANALYZING POTENTIAL GENOTOXIC IMPURITIES IN GLIFLOZINS

Abstract

The objective of this paper is to review the method development, optimize and validation of the method for the potential genotoxic impurities in gliflozins. The purpose of this validation is to show that processes involved in the development and manufacture of drug, production and analytical testing can be performed in an effective and reproducible manner. This review article provides guidance on how to perform validation characteristics for the analytical method which are utilized in pharmaceutical analysis. Key words: Analytical method development, Genotoxic impurities, Pharmaceutical analysis, Validation

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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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