Development and Validation of a Stability-indicating RP-HPLC Method for the Simultaneous Determination of Telmisartan and its Related Substances in Telmisartan Bulk Drug Substance-Reference-Cited by-同舟云学术

Development and Validation of a Stability-indicating RP-HPLC Method for the Simultaneous Determination of Telmisartan and its Related Substances in Telmisartan Bulk Drug Substance

Published:2020-09-02 Issue:5 Volume:10 Page:577-589
ISSN:2229-7928
Container-title:Analytical Chemistry Letters
language:en
Short-container-title:Analytical Chemistry Letters

Author:

Gholave Jayram V.¹,Gadhari Nayan S.²,Patil Suyog S.³,Upadyay Sharad S.²,Patil Vishwanath R.²,Shelke Kiran F.⁴

Affiliation:

1. Department of Applied Chemistry, Sardar Patel College of Engineering, Andheri (W), Mumbai-400058 (MS), India

2. Department of Chemistry, University of Mumbai Mumbai (MS), India

3. Forensic Science Laboratory, Aurangabad (MS), India

4. Late Pushpadevi Patil Arts and Science College, Risod, Dist. Washim (MS), India

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/22297928.2020.1850348

Reference22 articles.

1. Definition of Metabolic Syndrome

2. WHO/NCD/NCS/99.2, Geneva, Switzerland, (1999). Definition, diagnosis and classification of diabetes mellitus and its complications, Department of Noncommunicable Disease Surveillance.

3. Quantitative bio-analysis of pitavastatin and candesartan in rat plasma by HPLC-UV: Assessment of pharmacokinetic drug-drug interaction

4. Telmisartan

5. Validated specific densitometric method for simultaneous estimation of telmisartan and atorvastatin in presence of degradation products formed under ICH-recommended stress conditions

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