Literature DB >> 15497690

Assessment of the potential skin irritation of lysine-derivative anionic surfactants using mouse fibroblasts and human keratinocytes as an alternative to animal testing.

L Sanchez1, M Mitjans, M R Infante, M P Vinardell.   

Abstract

PURPOSE: The aim of this study was to identify new surfactants with low skin irritant properties for use in pharmaceutical and cosmetic formulations, employing cell culture as an alternative method to in vivo testing. In addition, we sought to establish whether potential cytotoxic properties were related to the size of the counterions bound to the surfactants.
METHODS: Cytotoxicity was assessed in the mouse fibroblast cell line 3T6 and the human keratinocyte cell line NCTC 2544 using the MTT assay and uptake of the vital dye neutral red 24 h after dosing (NRU).
RESULTS: Lysine-derivative surfactants showed higher IC50s than did commercial anionic irritant compounds such as sodium dodecyl sulfate, proving to be no more harmful than amphoteric betaines. The aggressiveness of the surfactants depended on the size of their constituent counterions: surfactants associated with lighter counterions showed a proportionally higher aggressivity than those with heavier ones.
CONCLUSIONS: Synthetic lysine-derivative anionic surfactants are less irritant than commercial surfactants such as sodium dodecyl sulfate and hexadecyltrimethylammonium bromide and are similar to betaines. These surfactants may offer promising applications in pharmaceutical and cosmetic preparations, representing a potential alternative to commercial anionic surfactants as a result of their low irritancy potential.

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Year:  2004        PMID: 15497690     DOI: 10.1023/b:pham.0000041459.63362.6f

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  20 in total

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4.  Possible effects of counterions on biological activities of anionic surfactants.

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Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2001-04       Impact factor: 3.228

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Authors:  Montserrat Mitjans; Verónica Martínez; Pere Clapés; Lourdes Pérez; M Rosa Infante; M Pilar Vinardell
Journal:  Pharm Res       Date:  2003-10       Impact factor: 4.200

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