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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1995-7-7
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pubmed:abstractText |
We report a new gas chromatography-mass spectrometry (GC-MS) method of measurement of red blood cell folates utilizing a stable isotope-labeled bacterial synthesized folate internal standard. The GC-MS method exploits the fact that the common feature of all folate molecules is a p-aminobenzoic acid moiety sandwiched between a pteridine ring and a polyglutamate chain of varying length. In this method, red blood cell folates together with a folate internal standard are specifically purified using bovine folate binding protein and the folates are subsequently chemically cleaved to p-aminobenzoic acid, pteridines, and glutamic acids. Since all six carbon atoms of the benzene ring in the p-aminobenzoic acid moiety of the folate internal standard are labeled with [13C], it is possible to use selected ion monitoring and stable isotope dilution GC-MS to quantitate folates. The method appears to be sensitive, specific, and accurate. The method has been applied to generate a reference range of red blood cell folates based on assay of 25 normal individuals.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4-Aminobenzoic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Carbon Isotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Folate Receptors, GPI-Anchored,
http://linkedlifedata.com/resource/pubmed/chemical/Folic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0003-2697
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
225
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:7778757-4-Aminobenzoic Acid,
pubmed-meshheading:7778757-Animals,
pubmed-meshheading:7778757-Carbon Isotopes,
pubmed-meshheading:7778757-Carrier Proteins,
pubmed-meshheading:7778757-Cattle,
pubmed-meshheading:7778757-Erythrocytes,
pubmed-meshheading:7778757-Folate Receptors, GPI-Anchored,
pubmed-meshheading:7778757-Folic Acid,
pubmed-meshheading:7778757-Gas Chromatography-Mass Spectrometry,
pubmed-meshheading:7778757-Humans,
pubmed-meshheading:7778757-Isotope Labeling,
pubmed-meshheading:7778757-Lactobacillus,
pubmed-meshheading:7778757-Receptors, Cell Surface,
pubmed-meshheading:7778757-Reference Standards,
pubmed-meshheading:7778757-Reproducibility of Results,
pubmed-meshheading:7778757-Sensitivity and Specificity
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pubmed:year |
1995
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pubmed:articleTitle |
Quantitation of red blood cell folates by stable isotope dilution gas chromatography-mass spectrometry utilizing a folate internal standard.
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pubmed:affiliation |
Division of Hematology, University of Colorado Health Sciences Center, Denver, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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