Characterization, in vitro dissolution, and pharmacokinetics of different batches of efavirenz raw materials-Reference-Cited by-同舟云学术

Characterization, in vitro dissolution, and pharmacokinetics of different batches of efavirenz raw materials

Published:2021-05-04 Issue:5 Volume:47 Page:725-734
ISSN:0363-9045
Container-title:Drug Development and Industrial Pharmacy
language:en
Short-container-title:Drug Development and Industrial Pharmacy

Author:

Bedor Danilo César Galindo¹,Bedor Noely Camila Tavares Cavalcanti¹,Neto João Gomes Pontes¹,José de Alencar Danda Lucas¹^ORCID,de Oliveira Flávio Martins²,de Oliveira Guilherme Henrique Onório²,Soares Sobrinho José Lamartine¹,Beyssac Eric³,Castro Whocely Victor de²,Santana Davi Pereira de¹

Affiliation:

1. Department of Pharmaceutical Sciences, Federal University of Pernambuco, Recife, Brazil

2. Graduate Program in Pharmaceutical Sciences, Federal University of São João del-Rei, Divinópolis Brazil

3. Biopharmaceutical Department, Faculty of Pharmacy, Université Clermont-Auvergne, Clermont, France

Publisher

Informa UK Limited

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03639045.2021.1934860

Reference57 articles.

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2. FDA. Susvita. In: Research CfDEa, editor. Silver Spring (MD): U.S. Department of Health and Human Services; 2019.

3. Dissolution enhancement of efavirenz by solid dispersion and PEGylation techniques

4. An improved kinetics approach to describe the physical stability of amorphous solid dispersions

5. Pharmacokinetic variability of antiretroviral drugs and correlation with virological outcome: 2 years of experience in routine clinical practice

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