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Validated stability indicating chromatographic method for determination of baricitinib and its degradation products in their tablet dosage form: Implementation to content uniformity and in vitro dissolution studies
Affiliation:1. Department of Analytical Chemistry, Faculty of Pharmacy, Erzincan Binali Yildirim University, 24100 Erzincan, Turkey;2. Department of Analytical Chemistry, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey;3. Department of Pharmacology, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey;1. Department of Human Physiology, University of Maiduguri, Borno State, Nigeria;2. Department of Human Anatomy, University of Maiduguri, Borno State, Nigeria;1. Université d’Angers, Faculté de Santé, Département Pharmacie, 16, Boulevard Daviers, 49045 Angers, France;2. Université d’Angers, Lab’UA, BU Belle Beille, 5, rue Le Nôtre, 49045 Angers, France;1. Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Damanhour University, Egypt;2. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Damanhour University, Egypt;1. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam-3, Andhra Pradesh, India;2. Aurobindo Pharma Limited, Bachupally, R.R District, Hyderabad-90, India
Abstract:
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Scheme 1: Graphical Abstract for the proposed method.Schéma 1 : Résumé graphique de la méthode proposée.
Keywords:Baricitinib  Content uniformity  In-vitro Dissolution  FDA  Stability-indicating RP-HPLC  baricitinib  Uniformité du contenu  dissolution in vitro  FDA  RP-HPLC indiquant la stabilité
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