Quantification of Oxidized and Unsaturated Bile Alcohols in Sea Lamprey Tissues by Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

Quantification of Oxidized and Unsaturated Bile Alcohols in Sea Lamprey Tissues by Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

A sensitive and reliable method was developed and validated for the determination of unsaturated bile alcohols in sea lamprey tissues using liquid-liquid extraction and ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The liver, kidney, and intestine samples were...

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Bibliographic Details
Published in:Molecules (Basel, Switzerland) Vol. 21; no. 9; p. 1119
Main Authors: Li, Ke, Scott, Anne M, Chung-Davidson, Yu-Wen, Bussy, Ugo, Patel, Trinkal, Middleton, Zoe E, Li, Weiming
Format: Journal Article
Language:English
Published: Switzerland MDPI 24-08-2016
MDPI AG
Subjects:
Animals
Cholestanols - chemistry
Cholestanols - metabolism
Chromatography, High Pressure Liquid
fish
Lampreys - metabolism
Mass Spectrometry
metabolites
Oxidation-Reduction
sulfated bile alcohol
UPLC-MS/MS
UPLC-MS/MS
metabolites
fish
sulfated bile alcohol
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Summary:A sensitive and reliable method was developed and validated for the determination of unsaturated bile alcohols in sea lamprey tissues using liquid-liquid extraction and ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The liver, kidney, and intestine samples were extracted with acetonitrile and defatted by n-hexane. Gradient UHPLC separation was performed using an Acquity BEH C18 column with a mobile phase of water and methanol containing 20 mM triethylamine. Multiple reaction monitoring modes of precursor-product ion transitions for each analyte was used. This method displayed good linearity, with correlation coefficients greater than 0.99, and was validated. Precision and accuracy (RSD %) were in the range of 0.31%-5.28%, while mean recoveries were between 84.3%-96.3%. With this technique, sea lamprey tissue samples were analyzed for unsaturated bile alcohol analytes. This method is practical and particularly suitable for widespread putative pheromone residue analysis.
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ISSN:1420-3049
1420-3049
DOI:10.3390/molecules21091119