Source:http://linkedlifedata.com/resource/pubmed/id/10971091
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-1-10
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pubmed:abstractText |
An assay based on stable isotope dilution liquid chromatography-tandem mass spectrometry (ID/LC-MS-MS) was developed for the quantification of 17-hydroxyprogesterone, the most important indicator of 21-hydroxylase deficiency in human plasma. Plasma was extracted using ethyl acetate and Extrelut columns. LC was performed on a reversed-phase C18 column using a water/methanol gradient. A benchtop triple quadrupole mass spectrometer, operating in selected reaction monitoring mode, served as mass detector. The analytical run time was 9 min per sample. The sensitivity was high: 0.06 pmol of 17-hydroxyprogesterone yielded a signal-to-noise ratio of 13. Precision (CV) and accuracy (relative error) derived from the analyses of unspiked and spiked validation samples were 7.4-12.0% and 6.4%, respectively. When analyzing the same samples - median (range), in nanomoles per liter - from neonates and adults independently by ID/LC-MS-MS as well as by ID/gas chromatography (GC)-MS, corresponding results were obtained: neonates (n = 10), ID/LC-MS-MS 3.99 (0.48-16.05), ID/GC-MS 5.39 (1.57-13.02); adults (n = 10), ID/LC-MS-MS 2.66 (1.39-6.15), ID/GC-MS 2.54 (0.51-5.12). The technique permitted reliable detection of classical and nonclassical forms of 21- hydroxylase deficiency. The much simpler sample preparation, the faster analytical run time and the operational ease possible with ID/LC-MS-MS permit a considerable increase of sample testing per day without compromising on analytical sensitivity and specificity. We expect that benchtop tandem mass spectrometry will open new avenues in clinical steroid analysis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0301-0163
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2000 S. Karger AG, Basel
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pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
68-71
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10971091-17-alpha-Hydroxyprogesterone,
pubmed-meshheading:10971091-Adrenal Hyperplasia, Congenital,
pubmed-meshheading:10971091-Adult,
pubmed-meshheading:10971091-Chromatography, Liquid,
pubmed-meshheading:10971091-Deuterium,
pubmed-meshheading:10971091-Female,
pubmed-meshheading:10971091-Humans,
pubmed-meshheading:10971091-Indicator Dilution Techniques,
pubmed-meshheading:10971091-Infant, Newborn,
pubmed-meshheading:10971091-Male,
pubmed-meshheading:10971091-Mass Spectrometry,
pubmed-meshheading:10971091-Reference Values,
pubmed-meshheading:10971091-Sensitivity and Specificity
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pubmed:year |
2000
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pubmed:articleTitle |
Determination of 17-hydroxyprogesterone in plasma by stable isotope dilution/benchtop liquid chromatography-tandem mass spectrometry.
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pubmed:affiliation |
Steroid Laboratory, Department of Pediatrics, University of Ulm, Germany. stefan.wudy@medizin.uni-ulm.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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