Development of an efficient stability‐indicating LC–MS/MS method for the analysis of selexipag and characterization of its degradation products

Author:

Amara Babu Namburi L. A.1,Koganti Kalyani1,Palakeeti Babji2,Srinivas Koduri S. V.3,Rao Koya Prabhakara1ORCID

Affiliation:

1. New Generation Materials Lab (NGML), Department of Science and Humanities Vignan's Foundation for Science, Technology and Research (VFSTR) (Deemed to be University), Vadlamudi Guntur Andhra Pradesh India

2. Department of Chemistry National Institute of Technology Warangal Telangana India

3. Syngene International LTD, Bommasandra Bangalore Karnataka India

Publisher

Wiley

Subject

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

Reference23 articles.

1. Stability indicating assay method development and validation for selexipag in pharmaceutical dosage form;Aashka Joshi M. S.;World Journal of Pharmaceutical Research,2020

2. Bioanalytical LC-MS/MS method for Determination and comparison of Selexipag Assay in various Biological materials and its Application to Pharmacokinetics Studies in Rat plasma

3. Hyperthyroidism and other causes of thyrotoxicosis: Management guideline of the American thyroid association and American association of clinical endoclinologists;Bahn C. R. S.;Thyroid,2010

4. Development and validation of bioanalytical method for the quantitative estimation of Selexipag in biological matrices using LC‐MS/MS;Bhadru B.;Journal of Pharmaceutical Sciences and Research,2019

5. Mechanisms and modifiers of reflex induced cutaneous vasodilation and vasoconstriction in humans

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