Forced degradation study of racecadotril: Effect of co-solvent, characterization of degradation products by UHPLC-Q-TOF-MS/MS, NMR and cytotoxicity assay-Reference-Cited by-同舟云学术

Forced degradation study of racecadotril: Effect of co-solvent, characterization of degradation products by UHPLC-Q-TOF-MS/MS, NMR and cytotoxicity assay

Published:2016-09 Issue: Volume:128 Page:9-17
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Chiguru Vishnuvardhan,Lingesh Allakonda,R. Srinivas,N. Satheeshkumar

Funder

Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Govt. of India

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference22 articles.

1. An overview of clinical studies with racecadotril in adults;Lecomte;Int. J. Antimicrob. Agents,2000

2. Racecadotril: a new approach to the treatment of diarrhea;Schwartz;Int. J. Antimicrob. Agents,2000

3. A blind, randomized comparison of racecadotril and loperamide for stopping acute diarrhea in adults;Wang;World J. Gastroenterol.,2005

4. A critical review on the use of modern sophisticated hyphenated tools in the characterization of impurities and degradation products;Singh;J. Pharm. Biomed. Anal.,2012

5. Stability-indicating methods for the determination of racecadotril in the presence of its degradation products;Mohamed;Biosci. Trend.,2009

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