Development and validation of GC–MS method for the determination of methyl methanesulfonate and ethyl methanesulfonate in imatinib mesylate-Reference-Cited by-同舟云学术

Development and validation of GC–MS method for the determination of methyl methanesulfonate and ethyl methanesulfonate in imatinib mesylate

Published:2008-03 Issue:4 Volume:46 Page:780-783
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Ramakrishna K.,Raman N.V.V.S.S.,Rao K.M.V. Narayana,Prasad A.V.S.S.,Reddy K. Subhaschander

Publisher

Elsevier BV

Subject

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

Reference11 articles.

1. IARC Monographs Program on the Evaluation of Carcinogenic Risks to Humans for Methyl Methanesulfonate, 71 (1999) 1059.

2. IARC Monographs Program on the Evaluation of Carcinogenic Risks to Humans for Ethyl Methanesulfonate, 7 (1974) 245.

3. Low level determination of p-toluenesulfonate and benzenesulfonate esters in drug substance by high performance liquid chromatography/mass spectrometry

4. The European Agency for the Evaluation of Medicinal Products, ICH Topic S1B, Note for Guidance on Carcinogenicity: Testing for Carcinogenicity of Pharmaceuticals, CPMP/ICH/299/95, 1998.

5. European Medicines Agency, Evaluation of Medicines for Human Use, Guideline on the Limits of Genotoxic Impurities, CPMP/SWP/5199/02, EMEA/CHMP/QWP/251344/2006, 2007.

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