Source:http://linkedlifedata.com/resource/pubmed/id/20116351
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5-6
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pubmed:dateCreated |
2010-2-15
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pubmed:abstractText |
An assay to quantify several possible breast cancer peptide biomarkers in human serum has been developed and validated, using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). The peptides include bradykinin, Hyp(3)-bradykinin, des-Arg(9)-bradykinin and fragments of fibrinogen alpha-chain (Fib-alpha([605-629])), inter-alpha-trypsin inhibitor heavy chain 4 (ITIH(4[666-687])) and complement component 4a (C4a([1337-1350])). Ile(13)-ITIH(4[666-687]), d20-C4a([1337-1350]) and Sar-D-Phe(8)-des-Arg(9)-bradykinin were used as internal standards. Bovine plasma, with 2 mM captopril and 2 mM D-L-mercaptoethanol-3-guanidino-ethylthiopropanoic acid (MEGETPA) to prevent rapid degradation of the bradykinins, was used as analyte-free matrix. Recoveries for solid-phase extraction (SPE) on mixed-mode weak cation exchange sorbents were between 62 and 90%. Multiple reaction monitoring (MRM) on a triple quadrupole mass spectrometer equipped with a heated electrospray source (H-ESI), operating in the positive ion-mode, was used for detection. The assay was fully validated and stabilities of the peptides were extensively explored. Bradykinin (10-500 ng/ml), Hyp(3)-bradykinin (4-200 ng/ml), des-Arg(9)-bradykinin (2-100 ng/ml), Fib-alpha([605-629]) (120-3000 ng/ml), ITIH(4[666-687]) (0.4-10 ng/ml) and C4a([1337-1350]) (1-25 ng/ml) were simultaneously quantified with deviations from the nominal concentrations below 22% and intra- and inter-assay precisions below 15 and 20%, respectively, for all peptides at all concentrations. The method has been successfully applied to several serum samples from breast cancer patients and matched controls.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alpha-Globulins,
http://linkedlifedata.com/resource/pubmed/chemical/Bradykinin,
http://linkedlifedata.com/resource/pubmed/chemical/Complement C4a,
http://linkedlifedata.com/resource/pubmed/chemical/Fibrinogen,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological,
http://linkedlifedata.com/resource/pubmed/chemical/fibrinogen Aalpha,
http://linkedlifedata.com/resource/pubmed/chemical/inter-alpha-inhibitor
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1873-376X
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
878
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
590-602
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pubmed:meshHeading |
pubmed-meshheading:20116351-Alpha-Globulins,
pubmed-meshheading:20116351-Animals,
pubmed-meshheading:20116351-Bradykinin,
pubmed-meshheading:20116351-Breast Neoplasms,
pubmed-meshheading:20116351-Cattle,
pubmed-meshheading:20116351-Chromatography, Liquid,
pubmed-meshheading:20116351-Complement C4a,
pubmed-meshheading:20116351-Female,
pubmed-meshheading:20116351-Fibrinogen,
pubmed-meshheading:20116351-Humans,
pubmed-meshheading:20116351-Linear Models,
pubmed-meshheading:20116351-Plasma,
pubmed-meshheading:20116351-Sensitivity and Specificity,
pubmed-meshheading:20116351-Tandem Mass Spectrometry,
pubmed-meshheading:20116351-Tumor Markers, Biological
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pubmed:year |
2010
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pubmed:articleTitle |
Quantitative assay for six potential breast cancer biomarker peptides in human serum by liquid chromatography coupled to tandem mass spectrometry.
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pubmed:affiliation |
Utrecht University, Faculty of Science, Department of Pharmaceutical Sciences, Section of Biomedical Analysis, Division of Drug Toxicology, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands. I.vandenbroek@uu.nl
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pubmed:publicationType |
Journal Article,
Validation Studies
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