Determination and quantification of related substances and degradation products in bictegravir by full factorial design evaluated HPLC and mass spectrometry-Reference-Cited by-同舟云学术

Determination and quantification of related substances and degradation products in bictegravir by full factorial design evaluated HPLC and mass spectrometry

Published:2023 Issue:10 Volume:15 Page:1274-1285
ISSN:1759-9660
Container-title:Analytical Methods
language:en
Short-container-title:Anal. Methods

Author:

Kumar S. R. Jythesh¹²^ORCID,Rao Vandavasi Koteswara¹^ORCID,Katari Naresh Kumar¹^ORCID,Jyothi Narreddy Siva²,Kowtharapu Leela Prasad¹^ORCID

Affiliation:

1. Department of Chemistry, GITAM School of Science, Rudraram, Hyderabad, Telangana 502329, India

2. Department of Analytical Research, Aurobindo Pharma Limited Research Centre-II, Indrakaran (V), Kandi (M), Sangareddy-502329, Telangana, India

Abstract

Determining and quantifying novel impurities and degraded impurities of a drug product is always a continuous challenge to enhancing the drug quality for patients' safety.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Engineering,General Chemical Engineering,Analytical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/AY/D2AY02106D

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4. H.Lee , Pharmaceutical Industry Practices on Genotoxic Impurities , CRC Press , Boca Raton, FL, USA , 2014 , 10.1201/b17350

5. Drug impurity profiling strategies*1

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