Document Detail


Control and analysis of alkyl and benzyl halides and other related reactive organohalides as potential genotoxic impurities in active pharmaceutical ingredients (APIs).
MedLine Citation:
PMID:  18657926     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This paper continues the review of the relevant scientific literature associated with the control and analysis of potential genotoxic impurities (PGIs) in active pharmaceutical ingredients (APIs). The initial review [D.P. Elder, A. Teasdale, A.M. Lipczynski, J. Pharm. Biomed. Anal. 46 (2008) 1-8.] focused on the specific class of sulfonate esters but in this instance reference is made to the analysis of alkyl and benzyl halides and other related reactive organohalide alkylating agents. Such reactive materials are commonly employed in pharmaceutical research and development as raw materials, reagents and intermediates in the chemical synthesis of new drug substances. Consequently a great deal of attention and effort is extended by the innovative and ethical pharmaceutical industry to ensure that appropriate and practicable control strategies are established during drug development to ensure residues of such agents, as potential impurities in new drug substances, are either eliminated or minimized to such an extent so as to not present a significant safety risk to volunteers and patients in clinical trials and beyond. The reliable trace analysis of such reactive organohalides is central to such control strategies and invariably involves a state-of-the-art combination of high-resolution separation science techniques coupled to sensitive and selective modes of detection. This article reports on the most recent developments in the regulatory environment, overall strategies for the control of alkylating agents and the latest developments in analysis culminating in a literature review of analytical approaches. The literature is sub-categorized by separation technique (gas chromatography (GC), high-performance liquid chromatography (HPLC), thin layer chromatography (TLC) and capillary zone electrophoresis (CZE)) and further tabulated by API type and impurity with brief method details and references. As part of this exercise, a selection of relevant pharmacopoeial monographs was also reviewed. The continued reliance on relatively non-specific and insensitive TLC methodologies in several monographs was noteworthy.
Authors:
D P Elder; A M Lipczynski; A Teasdale
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Publication Detail:
Type:  Journal Article; Review     Date:  2008-06-25
Journal Detail:
Title:  Journal of pharmaceutical and biomedical analysis     Volume:  48     ISSN:  0731-7085     ISO Abbreviation:  J Pharm Biomed Anal     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-10-20     Completed Date:  2009-02-26     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8309336     Medline TA:  J Pharm Biomed Anal     Country:  England    
Other Details:
Languages:  eng     Pagination:  497-507     Citation Subset:  IM    
Affiliation:
GlaxoSmithKline R&D, Park Road, Ware SG12 0DP, UK. David.P.Elder@gsk.com
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MeSH Terms
Descriptor/Qualifier:
Alkylating Agents / analysis*
Chemistry, Pharmaceutical*
Drug Contamination*
Halogens / analysis*,  chemistry
Mutagens / analysis*,  chemistry
Pharmaceutical Preparations / analysis*,  chemical synthesis,  chemistry
Salts
Chemical
Reg. No./Substance:
0/Alkylating Agents; 0/Halogens; 0/Mutagens; 0/Pharmaceutical Preparations; 0/Salts

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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