| Literature DB >> 25128875 |
Lien Taevernier1, Lieselotte Veryser1, Kirsten Vandercruyssen1, Matthias D'Hondt1, Stijn Vansteelandt2, Sarah De Saeger3, Bart De Spiegeleer4.
Abstract
Currently, dermal exposure data of cyclic depsipeptide mycotoxins beauvericin and enniatins are completely absent with a lack of local skin and systemic kinetics, despite their widespread skin contact and intrinsic hazard. Therefore a sensitive and specific bioanalytical high-throughput UHPLC-MS/MS method was developed for the quantitative and simultaneous determination of cyclic depsipeptide mycotoxins beauvericin and enniatins (A, A1, B, B1, D, E, C/F) in human skin Franz diffusion cell samples. The limits of detection ranged between 10 and 17pg/ml, while the total run time was only 4.5min. There was no significant effect of endogenous skin compounds on the mycotoxin MS signal observed, and the accuracy (0.68-24.68% bias) and precision (0.57-10.70% RSD) were considered acceptable for our purposes. Moreover, it was demonstrated that these cyclic depsipeptides are stable for at least 7 days when formulated in different organic or aqueous mixtures. Finally, adsorption to glass did occur: at least 50% ethanol or acetonitrile is required to prevent significant adsorption effects, which could be as high as 45%.Entities:
Keywords: Adsorption; Beauvericin; Bioanalytical UHPLC-MS/MS method; Cyclic depsipeptide mycotoxins; Enniatins; Transdermal Franz diffusion cell
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Year: 2014 PMID: 25128875 DOI: 10.1016/j.jpba.2014.07.021
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935