Application of analytical quality by design (AQbD) for stability-indicating method development for quantification of nevirapine and its degradation products-Reference-Cited by-同舟云学术

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Application of analytical quality by design (AQbD) for stability-indicating method development for quantification of nevirapine and its degradation products

Published:2024-04 Issue: Volume:199 Page:109939
ISSN:0026-265X
Container-title:Microchemical Journal
language:en
Short-container-title:Microchemical Journal

Author:

Jesus do Nascimento Lopes Ivone de,Kazumasa Fujimori Sérgio,de Carvalho Mendes Thamara,Adrielle Dias de Almeida Rayza,Furtado de Mendonça de Sousa Flávia,Areias de Oliveira Camila,Dibo do Nascimento Diogo,Rebello Lourenço Felipe,Isabel Rodrigues Maria,Deris Prado Livia

Funder

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Publisher

Elsevier BV

Reference47 articles.

1. ICH, Analytical Procedure Development, Q8(R2), 2009.

2. Efficient drug development of oseltamivir capsules based on process control, bioequivalence and PBPK modeling;Medeiros;Drug Dev. Ind. Pharm.,2022

3. Dissolution method evaluation for carvedilol tablets;Alves;Dissolution Technol.,2020

4. A novel stability-indicating HPLC-DAD method for determination of favipiravir, a potential antiviral drug for COVID-19 treatment; application to degradation kinetic studies and in-vitro dissolution profiling;Marzouk;Microchem. J.,2022

5. Quality by design based development and validation of HPLC method for simultaneous estimation of paclitaxel and vinorelbine tartrate in dual drug loaded liposomes;Bonde;Microchem. J.,2019

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