Unique Quality by Design Approach for Developing HPLC and LC-MS Method for Estimation of Process and Degradation Impurities in Pibrentasvir, Antiviral Agent for Hepatitis C-Reference-Cited by-同舟云学术

Unique Quality by Design Approach for Developing HPLC and LC-MS Method for Estimation of Process and Degradation Impurities in Pibrentasvir, Antiviral Agent for Hepatitis C

Published:2022-12-15 Issue:51 Volume:7 Page:47650-47661
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Vemuri Divya Kumar¹,Akshinthala Parameswari²,Konduru Naresh³,Kowtharapu Leela Prasad⁴,Katari Naresh Kumar¹⁵,Jonnalagadda Sreekantha Babu⁵^ORCID,Gundla Rambabu¹^ORCID

Affiliation:

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

2. Department of Science and Humanities, MLR Institute of Technology, Dundigal, Medchal, Hyderabad 500 043, India

3. Analytical Research and Development, Zhuhai Resproly Pharmaceutical Technology Co., Ltd., Zhuhai, Guangdong province 519040, China

4. Analytical Research and Development, Wuxi STA (Wuxi app Tec) Pharmaceutical Co., Ltd., Wuxi, Jiangsu 214028, China

5. School of Chemistry & Physics, College of Agriculture, Engineering & Science, Westville Campus, University of KwaZulu-Natal, P Bag X 54001, Durban 4000, South Africa

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c04617

Reference20 articles.

1. A New Stability-Indicating RP-HPLC-Pda Method for Simultaneous Estimation of Glecaprevir and Pibrentasvir in tablet dosage form

2. Development of validated stability indicating RP-HPLC method for the estimation of glecaprevir and pibrentasvir in bulk and pharmaceutical dosage form

3. A New Force Indicating RP-HPLC Method Development and Validation for the Simultaneous Estimation of Pibrentasvir and Glecaprevir in Bulk and its Tablet Dosage Form

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