A simple, selective, and sensitive gas chromatography-mass spectrometry method for the analysis of five process-related impurities in atenolol bulk drug and capsule formulations-Reference-Cited by-同舟云学术

A simple, selective, and sensitive gas chromatography-mass spectrometry method for the analysis of five process-related impurities in atenolol bulk drug and capsule formulations

Published:2017-06-28 Issue:15 Volume:40 Page:3086-3093
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Sci.

Author:

Reddy Ambavaram Vijaya Bhaskar¹²,Yusop Zulkifli¹,Jaafar Jafariah²^ORCID,Bin Aris Azmi¹³,Abdul Majid Zaiton²

Affiliation:

1. Centre for Environmental Sustainability and Water Security (IPASA), Research Institute for Sustainable Environment; Universiti Teknologi Malaysia; Johor Bahru Malaysia

2. Department of Chemistry, Faculty of Science; Universiti Teknologi Malaysia; Johor Bahru Malaysia

3. Department of Environmental Engineering, Faculty of Civil Engineering; Universiti Teknologi Malaysia; Johor Bahru Malaysia

Funder

Ministry of Higher Education Malaysia

Universiti Teknologi Malaysia

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Reference23 articles.

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2. Recent advances in analysis of hazardous genotoxic impurities in pharmaceuticals by HPLC, GC and CE;Azzam;J. Liq. Chromatogr. Relat. Technol.,2016

3. Genotoxic impurities in pharmaceutical manufacturing: Sources, regulations, and mitigation;Gyorgy;Chem. Rev.,2015

4. Modern approaches to estimating the content of genotoxic impurities in drugs: A review;Matveeva;Pharm. Chem. J.,2016

5. Committee for medicinal products for human use (CHMP), Guideline on the limits of genotoxic impurities(EMEA/CHMP/QWP/251344/2006), Final version released in London on 28 June 2006

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