Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method-Reference-Cited by-同舟云学术

Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method

Published:2017-12-29 Issue:3 Volume:56 Page:270-284
ISSN:0021-9665
Container-title:Journal of Chromatographic Science
language:en
Short-container-title:

Author:

Mantripragada Murali Krishna V V N¹,Rao Sumathi V¹,Nutulapati Venugopal V S²,Mantena Bhaskara P V¹

Affiliation:

1. APL Research Centre (A Division of Aurobindo Pharma Limited), Survey No. 313, Bachupally, Quthubullapur Mandal, Rangareddy District, Hyderabad 500072, Telangana, India

2. GITAM University, Gandhi Nagar, Rushikonda, Visakhapatnam 530045, Andhra Pradesh, India

Funder

Aurobindo Pharma Research centre

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

Link

http://academic.oup.com/chromsci/article-pdf/56/3/270/24021378/bmx110.pdf

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3. Gradient RP-HPLC method for the determination of potential impurities in Atazanavir sulphate;Sreenivasa Rao;Journal of Pharmaceutical and Biomedical Analysis,2011

4. Determination of Atazanavir in the presence of its degradation products by a stability-indicating LC method;Seshachalam;Chromatographia,2007

5. Development and validation of a simple, sensitive, selective and stability-indicating RP-UPLC method for the quantitative determination of ritonavir and its related compounds;Srinivasarao;Journal of Chromatographic Science,2015

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