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Liquid Chromatography-Tandem Mass Spectrometric Analysis of Octaethylene Glycol Monodecyl Ether in Rat Plasma and its Application to Pharmacokinetic Studies

Authors
Kim, HyeonKim, Hyeong JunChoi, Min SunKim, In SookGye, Myung ChanYoo, Hye Hyun
Issue Date
May-2017
Publisher
Perston Publications, Inc.
Keywords
FATTY ALCOHOL ETHOXYLATES; NONIONIC SURFACTANTS; BIODEGRADATION; NONYLPHENOL; TOXICITY; PATHWAYS; HUMANS
Citation
Journal of Analytical Toxicology, v.41, no.4, pp 334 - 339
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
Journal of Analytical Toxicology
Volume
41
Number
4
Start Page
334
End Page
339
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/9653
DOI
10.1093/jat/bkw134
ISSN
0146-4760
1945-2403
Abstract
Alcohol ethoxylates (AEs) are a major class of non-ionic surfactants, which are widely used in household, institutional and industrial cleaners, and they are considered as an alternative of nonylphenol. In this study, a rapid, sensitive and reliable bioanalytical method was developed for the determination of octaethylene glycol monodecyl ether (C10E8, an AE) in rat plasma using liquid chromatography-tandem mass spectrometry (LC-MS-MS). Chromatographic separation was performed on a reversed-phase C18 column (2.1 mm x 50 mm, 2.1 mu m). The mobile phase consisted of 0.1% formic acid in distilled water and 0.1% formic acid in acetonitrile (40:60% v/v). The flow rate was 0.3 mL/min. For mass spectrometric detection, the multiple reaction monitoring (MRM) mode was used; the MRM transitions were m/z 511.5 -> m/z 133.1 for C10E8 and m/z 423.3 -> m/z 133.1 for hexaethylene glycol monodecyl ether (internal standard) in the positive ion mode. A calibration curve was constructed within the range of 2-2,000 ng/mL; the intra- (n = 5) and inter-day (n = 3) precision and accuracy were within 10%. The LC-MS-MS method was specific, accurate and reproducible, and this method was successfully applied in a pharmacokinetic study of C10E8 in rats. C10E8 was intravenously (1 mg/kg, n = 6) and orally (10 mg/kg, n = 7) administered to rats. The kinetic parameters were analyzed based on a noncompartmental statistical model using the pharmacokinetic modeling software (WinNonlin). The oral bioavailability of C10E8 was 34.4%.
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