Development and validation of a stability‐indicating UPLC method for the determination of olmesartan medoxomil, amlodipine and hydrochlorothiazide degradation impurities in their triple‐combination dosage form using factorial design of experiments-Reference-Cited by-同舟云学术

Development and validation of a stability‐indicating UPLC method for the determination of olmesartan medoxomil, amlodipine and hydrochlorothiazide degradation impurities in their triple‐combination dosage form using factorial design of experiments

Published:2021-06-28 Issue:11 Volume:35 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Marisetti Vishnu Murthy¹²^ORCID,Katakam Prakash¹²,Siddhani Vijaya Krishna²³,Katari Naresh Kumar²

Affiliation:

1. Analytical Research and Development ScieGen Pharmaceuticals Inc. Hauppauge NY USA

2. Department of Chemistry GITAM University Hyderabad Telangana India

3. Regulatory Affairs, ScieGen Pharmaceuticals Inc. Hauppauge NY USA

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bmc.5194

Reference31 articles.

1. A QBD WITH DESIGN-OF-EXPERIMENTS APPROACH FOR DEVELOPMENT OF A STATE-OF-THE-ART UPLC PURITY METHOD FOR CARBAMAZEPINE

2. Simultaneous estimation of olmesartan medoxomil and hydrochlorothiazide by RP‐HPLC method from combined dosage forms;Ashok Kumar J.;International Journal of Research in Pharmaceutical Sciences,2010

3. Validated HPTLC method for simultaneous determination of quinapril hydrochloride and hydrochlorothiazide in a tablet dosage form

4. Derivative and Q-analysis spectrophotometric methods for estimation of hydrochlorothiazide and olmesartan medoxomil in tablets

5. Development of forced degradation and stability indicating studies of drugs—A review

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