A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood. / Monosik, Rastislav; Dragsted, Lars Ove.

I: Analytical Methods, Bind 8, Nr. 38, 2016, s. 6865-6871.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Monosik, R & Dragsted, LO 2016, 'A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood', Analytical Methods, bind 8, nr. 38, s. 6865-6871. https://doi.org/10.1039/C6AY01908K

APA

Monosik, R., & Dragsted, L. O. (2016). A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood. Analytical Methods, 8(38), 6865-6871. https://doi.org/10.1039/C6AY01908K

Vancouver

Monosik R, Dragsted LO. A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood. Analytical Methods. 2016;8(38):6865-6871. https://doi.org/10.1039/C6AY01908K

Author

Monosik, Rastislav ; Dragsted, Lars Ove. / A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood. I: Analytical Methods. 2016 ; Bind 8, Nr. 38. s. 6865-6871.

Bibtex

@article{43b8d62145ce41d4b7d0c440673cee42,
title = "A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood",
abstract = "Alcohol intake has been associated with preventive as well as negative effects on health. However, the intake estimates are often based on subjective reporting and therefore biased and the types of beverages consumed are often inaccurately reported. Accurate and specific quantification of alcohol related compounds in biological samples may help to understand dietary exposure and metabolic kinetics. The aim of this study was to develop a simple, rapid and versatileUHPLC–MSMS method able of quantifying various alcohol derived compounds or potential effect markers. The method was thoroughly validated for L–tartaric acid, ethyl sulphate, ethyl–β–D–glucuronide, indoxyl sulphate, p–cresol sulphate,resveratrol, estrone sulphate and dihydroepiandrosterone sulphate. Isocohumulone and isoxanthohumol related to beer intake were also evaluated and the former found to be detectable but no standards were available for final analytical validation. All selected analytes were analyzed within 6 minutes using negative ionization mode and multiple reaction monitoring.",
author = "Rastislav Monosik and Dragsted, {Lars Ove}",
note = "CURIS 2016 NEXS 248",
year = "2016",
doi = "10.1039/C6AY01908K",
language = "English",
volume = "8",
pages = "6865--6871",
journal = "Analytical Methods",
issn = "1759-9660",
publisher = "Royal Society of Chemistry",
number = "38",

}

RIS

TY - JOUR

T1 - A versatile UHPLC–MSMS method for simultaneous quantification of various alcohol intake related compounds in human urine and blood

AU - Monosik, Rastislav

AU - Dragsted, Lars Ove

N1 - CURIS 2016 NEXS 248

PY - 2016

Y1 - 2016

N2 - Alcohol intake has been associated with preventive as well as negative effects on health. However, the intake estimates are often based on subjective reporting and therefore biased and the types of beverages consumed are often inaccurately reported. Accurate and specific quantification of alcohol related compounds in biological samples may help to understand dietary exposure and metabolic kinetics. The aim of this study was to develop a simple, rapid and versatileUHPLC–MSMS method able of quantifying various alcohol derived compounds or potential effect markers. The method was thoroughly validated for L–tartaric acid, ethyl sulphate, ethyl–β–D–glucuronide, indoxyl sulphate, p–cresol sulphate,resveratrol, estrone sulphate and dihydroepiandrosterone sulphate. Isocohumulone and isoxanthohumol related to beer intake were also evaluated and the former found to be detectable but no standards were available for final analytical validation. All selected analytes were analyzed within 6 minutes using negative ionization mode and multiple reaction monitoring.

AB - Alcohol intake has been associated with preventive as well as negative effects on health. However, the intake estimates are often based on subjective reporting and therefore biased and the types of beverages consumed are often inaccurately reported. Accurate and specific quantification of alcohol related compounds in biological samples may help to understand dietary exposure and metabolic kinetics. The aim of this study was to develop a simple, rapid and versatileUHPLC–MSMS method able of quantifying various alcohol derived compounds or potential effect markers. The method was thoroughly validated for L–tartaric acid, ethyl sulphate, ethyl–β–D–glucuronide, indoxyl sulphate, p–cresol sulphate,resveratrol, estrone sulphate and dihydroepiandrosterone sulphate. Isocohumulone and isoxanthohumol related to beer intake were also evaluated and the former found to be detectable but no standards were available for final analytical validation. All selected analytes were analyzed within 6 minutes using negative ionization mode and multiple reaction monitoring.

U2 - 10.1039/C6AY01908K

DO - 10.1039/C6AY01908K

M3 - Journal article

VL - 8

SP - 6865

EP - 6871

JO - Analytical Methods

JF - Analytical Methods

SN - 1759-9660

IS - 38

ER -

ID: 164573100