Characterization of imatinib mesylate formulations distributed in South American countries: Determination of genotoxic impurities by UHPLC-MS/MS and dissolution profile-Reference-Cited by-同舟云学术

Characterization of imatinib mesylate formulations distributed in South American countries: Determination of genotoxic impurities by UHPLC-MS/MS and dissolution profile

Published:2018-04-06 Issue:7 Volume:32 Page:e4222
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Wolff Fernanda Caroline¹,Dillenburg Thaís Luise¹,Venzon Antunes Marina²,Linden Rafael²,Comparsi Wagner Sandrine³,Verza Simone G.¹^ORCID

Affiliation:

1. Bioanalysis Laboratory, Instituto de Ciências da Saúde; Universidade Feevale; Novo Hamburgo RS Brazil

2. Toxicological Analysis Laboratory, Instituto de Ciências da Saúde; Universidade Feevale; Novo Hamburgo RS Brazil

3. Diagnostics Methods Department; Fundação Universidade Federal de Ciências da Saúde de Porto Alegre; Porto Alegre RS Brazil

Funder

Feevale University

Publisher

Wiley

Subject

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

Reference27 articles.

1. ANVISA 2010 Resolução-RDC no. 31, de 11 de Agosto de 2010

2. Quantification of potential genotoxic impurity in imatinib mesylate by LC-MS/MS;Bhatt;Acta Chimica Pharmaceutica Indica,2013

3. Recent innovations in dissolution testing;Dressmann;Journal of Pharmacy and Pharmacology,2012

4. Centrosome aberrations after nilotinib and imatinib treatment in vitro are associated with mitotic spindle defects and genetic instability;Fabarius;British Journal of Haematology,2007

5. Fundamental and molecular mechanisms of mutagenesis: The influence of the extent of target organs on sensitivities of methods for screening rodent carcinogens;Fu;Mutation Research,1995

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2. Detection of Two Genotoxic Impurities in Drug Substance and Preparation of Imatinib Mesylate by LC–MS/MS;Chromatographia;2020-05-12