Stress degradation of edaravone: Separation, isolation and characterization of major degradation products

Author:

Baghel Madhuri1,Rajput Sadhana J.1

Affiliation:

1. Centre of Relevance and Excellence in Novel Drug Delivery Systems, Faculty of Pharmacy, G.H. Patel Building; The Maharaja Sayajirao University of Baroda; Vadodara Gujarat India

Funder

UGC-BSR (RFSMS)

Publisher

Wiley

Subject

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

Reference20 articles.

1. Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patients;Abe;Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration,2014

2. Fresh from the designation pipeline: Orphan drugs designated in the European Union;Antoniu;Expert Opinion on Orphan Drugs,2015

3. Development of stability indicating TLC-densitometry method of edaravone using QbD approach: Degradation kinetic study;Baghel;Indian Journal of Pharmaceutical Education and Research,2017

4. Development and validation of a simple UV spectrophotometric and isocratic RP-HPLC method for estimation of edaravone in bulk and it's injection formulation;Fanse;Indo American Journal of Pharmaceutical Research,2015

5. RP-HPTLC method for the in vitro estimation of edaravone in human plasma;Gandhimathi;Indian Journal of Pharmaceutical Science,2010

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