Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry

Analysis of catechol estrogens (2 & 4 hydroxy-estrone and estradiol) has proven troublesome by liquid chromatography tandem mass spectrometry due to their low concentrations, short half-lives and temperature-labile nature. Derivatization to methyl piperazine analogues has been reported for a pan...

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Main Authors: Nina Denver, Shazia Khan, Ioannis Stasinopoulos, Colin Church, Natalie Z.M. Homer, Margaret R. MacLean, Ruth Andrew
Format: Article
Language:English
Published: Elsevier 2019-04-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340919300897
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author Nina Denver
Shazia Khan
Ioannis Stasinopoulos
Colin Church
Natalie Z.M. Homer
Margaret R. MacLean
Ruth Andrew
author_facet Nina Denver
Shazia Khan
Ioannis Stasinopoulos
Colin Church
Natalie Z.M. Homer
Margaret R. MacLean
Ruth Andrew
author_sort Nina Denver
collection DOAJ
description Analysis of catechol estrogens (2 & 4 hydroxy-estrone and estradiol) has proven troublesome by liquid chromatography tandem mass spectrometry due to their low concentrations, short half-lives and temperature-labile nature. Derivatization to methyl piperazine analogues has been reported for a panel of 9 estrogens in, “Derivatization enhances analysis of estrogens and their bioactive metabolites in human plasma by liquid chromatography tandem mass spectrometry” (Denver et al., 2019). Data show alteration of the base catalyst in this method was required to allow detection of catechol estrogens to low levels. Data also highlight the challenges faced in chromatographic separation of isomers and isotopologues, which were partially overcome by employing an extended column length and reduced oven temperature. In addition, data analysis displayed significant matrix effects during quantitation in plasma, following solid-phase extraction, despite efficient recoveries.
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spelling doaj.art-2d75ca2bfc4040fd898baa7771185ed12022-12-22T00:50:39ZengElsevierData in Brief2352-34092019-04-0123Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometryNina Denver0Shazia Khan1Ioannis Stasinopoulos2Colin Church3Natalie Z.M. Homer4Margaret R. MacLean5Ruth Andrew6Mass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh, EH16 4TJ, United Kingdom; Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, University Avenue, Glasgow, G12 8QQ, United KingdomMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh, EH16 4TJ, United KingdomMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh, EH16 4TJ, United KingdomScottish Pulmonary Vascular Unit, Golden Jubilee National Hospital, Agamemnon St, Clydebank, G81 4DY, United KingdomMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh, EH16 4TJ, United KingdomStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral Street, Glasgow, G4 0RE, United KingdomMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh, EH16 4TJ, United Kingdom; Corresponding author.Analysis of catechol estrogens (2 & 4 hydroxy-estrone and estradiol) has proven troublesome by liquid chromatography tandem mass spectrometry due to their low concentrations, short half-lives and temperature-labile nature. Derivatization to methyl piperazine analogues has been reported for a panel of 9 estrogens in, “Derivatization enhances analysis of estrogens and their bioactive metabolites in human plasma by liquid chromatography tandem mass spectrometry” (Denver et al., 2019). Data show alteration of the base catalyst in this method was required to allow detection of catechol estrogens to low levels. Data also highlight the challenges faced in chromatographic separation of isomers and isotopologues, which were partially overcome by employing an extended column length and reduced oven temperature. In addition, data analysis displayed significant matrix effects during quantitation in plasma, following solid-phase extraction, despite efficient recoveries.http://www.sciencedirect.com/science/article/pii/S2352340919300897
spellingShingle Nina Denver
Shazia Khan
Ioannis Stasinopoulos
Colin Church
Natalie Z.M. Homer
Margaret R. MacLean
Ruth Andrew
Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
Data in Brief
title Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
title_full Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
title_fullStr Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
title_full_unstemmed Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
title_short Data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
title_sort data for analysis of catechol estrogen metabolites in human plasma by liquid chromatography tandem mass spectrometry
url http://www.sciencedirect.com/science/article/pii/S2352340919300897
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