Document Detail


The utility of sulfonate salts in drug development.
MedLine Citation:
PMID:  20112423     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The issue of controlling genotoxic impurities in novel active pharmaceutical ingredients (APIs) is a significant challenge. Much of the current regulatory concern, has been focused on the formation and control of genotoxic sulfonate esters. This is linked with the withdrawal of Viracept (Nefinavir mesilate) from European markets in mid-2007, over concerns about elevated levels of ethyl methanesulfonate (EMS). This issue has resulted in calls from European regulators to assess risk mitigation strategies for all marketed products employing a sulfonic acid counter-ion to ensure that the sulfonate esters that could be potentially formed are controlled to threshold of toxicological concern (TTC)-based limits. This has even led to calls to avoid sulfonic acids as salt counter-ions. However, sulfonic acid salts possess a range of properties that are useful to both synthetic and formulation chemists. Whilst sulfonate salts are not a universal panacea to some of the problems of salt formation they do offer significant advantages as alternatives to other salt forming moieties under certain circumstances. This review thus sets out to define some of the advantages provided through utilization of sulfonic acids, explaining the importance of their retention as part of a thorough salt selection process.
Authors:
David P Elder; Ed Delaney; Andrew Teasdale; Steve Eyley; Van D Reif; Karine Jacq; Kevin L Facchine; Rolf Schulte Oestrich; Patrick Sandra; Frank David
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Journal of pharmaceutical sciences     Volume:  99     ISSN:  1520-6017     ISO Abbreviation:  J Pharm Sci     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-04-30     Completed Date:  2010-08-02     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985195R     Medline TA:  J Pharm Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2948-61     Citation Subset:  IM    
Copyright Information:
(c) 2010 Wiley-Liss, Inc. and the American Pharmacists Association
Affiliation:
GlaxoSmithKline Research and Development, Park Road, Ware, Hertfordshire SG12 0DP, United Kingdom. david.p.elder@gsk.com
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MeSH Terms
Descriptor/Qualifier:
Animals
Drug Discovery*
Humans
Salts / chemistry*,  pharmacology
Sulfonic Acids / chemistry*,  pharmacology
Chemical
Reg. No./Substance:
0/Salts; 0/Sulfonic Acids

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