A simple high‐performance liquid chromatography method development for Carbidopa and Levodopa impurities: Evaluation of risk assessment before method validation by Quality by Design approach-Reference-Cited by-同舟云学术

A simple high‐performance liquid chromatography method development for Carbidopa and Levodopa impurities: Evaluation of risk assessment before method validation by Quality by Design approach

Published:2020-10-26 Issue:11-12 Volume:3 Page:530-539
ISSN:2573-1815
Container-title:SEPARATION SCIENCE PLUS
language:en
Short-container-title:Sep Sci plus

Author:

Subramanian Velusamy B.¹,Konduru Naresh²,Katari Naresh Kumar¹^ORCID,Dongala Thirupathi¹³^ORCID,Gundla Rambabu¹

Affiliation:

1. Department of Chemistry, School of Science GITAM (Deemed to be University) Hyderabad, Rudraram Sangareddy India

2. Quality Research and Development Zhejiang Xianju Pharmaceutical Co., Ltd. Zhejiang P. R. China

3. Department of Quality control Aurex Laboratories LLC East Windsor New Jersey USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/sscp.202000029

Reference33 articles.

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2. Development and validation of stability – indication RP‐HPLC assay method for Entacapone in entacapone tablets;Raj Kumar D;Int J Pharm Sci Res,2013

3. Stability indicating method for the determination of Levodopa – carbidopa and related impurity;Johan BK;J Chromat A,1994

4. Simultaneous estimation of Levodopa, carbidopa and Entacapone in pharmaceutical dosage by validated reverse phase high‐performance liquid chromatography;Maitreyi Z;Int J Instit Pharm Lif Sci,2012

5. Development and validation of RP‐HPLC method for simultaneous estimation of Levodopa and carbidopa in pharmaceutical dosage forms;Suresh Kumar S;J Pharm Rese,2011

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