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dc.contributor.authorLaszlo, CF
dc.contributor.authorPaz Montoya, J
dc.contributor.authorShamseddin, M
dc.contributor.authorDe Martino, F
dc.contributor.authorBeguin, A
dc.contributor.authorNellen, R
dc.contributor.authorBruce, SJ
dc.contributor.authorMoniatte, M
dc.contributor.authorHenry, H
dc.contributor.authorBrisken, C
dc.date.accessioned2020-08-28T09:04:43Z
dc.date.issued2019-10-25
dc.identifier.citationJournal of pharmaceutical and biomedical analysis, 2019, 175 pp. 112756 - ?
dc.identifier.issn0731-7085
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4049
dc.identifier.eissn1873-264X
dc.identifier.doi10.1016/j.jpba.2019.07.004
dc.description.abstractIn the context of hormonal contraception and hormone replacement therapy (HRT), many women are exposed to exogenous hormones. Current use of hormonal contraception with combined ethinyl estradiol and different progestins bestows a breast cancer relative risk (RR) of 1.2- while combined HRT has a RR of 2. Although these exposures present an important public health issue, little is known about the effects of individual progestins on the breast and other tissues. Increasing availability of large scale biobanks, high throughput analyses and data management tools enable ever expanding, sophisticated population studies. In order to address the impact of distinct progestins on various health indicators, it is desirable to accurately quantify progestins in clinical samples. Here we have developed and validated a high resolution liquid chromatography mass spectrometry (LC-MS) targeted method for the simultaneous quantification of 11 synthetic progestins widely used in oral contraceptives, gestodene, levonorgestrel, etonogestrel, chlormadinone acetate, cyproterone acetate, drospirenone, desacetyl norgestimate, medroxyprogesterone acetate, norethindrone, dienogest, nomegestrol acetate, and 4 endogenous steroid hormones, progesterone, testosterone, androstenedione, and cortisol in blood samples. This highly specific quantitative analysis with high resolution Orbitrap technology detects and quantifies 15 compounds using their internal standard counterparts in a single 12 min LC-MS run. Sensitivity is attained by the use of the instrument in targeted selected ion monitoring mode. Lower limit of quantitation ranges from 2.4 pg/ml for drospirenone to 78.1 pg/ml for chlormadinone acetate. The method provides comprehensive progestin panel measurements with as little as 50 μl of murine or human plasma.
dc.formatPrint-Electronic
dc.format.extent112756 - ?
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.subjectAnimals
dc.subjectMice, Inbred NOD
dc.subjectHumans
dc.subjectMice
dc.subjectSteroids
dc.subjectContraceptive Agents
dc.subjectProgestins
dc.subjectChromatography, Liquid
dc.subjectFemale
dc.subjectTandem Mass Spectrometry
dc.titleA high resolution LC-MS targeted method for the concomitant analysis of 11 contraceptive progestins and 4 steroids.
dc.typeJournal Article
dcterms.dateAccepted2019-07-02
rioxxterms.versionofrecord10.1016/j.jpba.2019.07.004
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.licenseref.startdate2019-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfJournal of pharmaceutical and biomedical analysis
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Endocrine control mechanisms
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Endocrine control mechanisms
pubs.publication-statusPublished
pubs.volume175
pubs.embargo.termsNot known
icr.researchteamEndocrine control mechanisms
dc.contributor.icrauthorBrisken, Cathrin


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0