Source:http://linkedlifedata.com/resource/pubmed/id/21036678
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rdf:type | |
lifeskim:mentions |
umls-concept:C0001554,
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umls-concept:C0023884,
umls-concept:C0025663,
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umls-concept:C0068154,
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umls-concept:C0524527,
umls-concept:C0680730,
umls-concept:C1148554,
umls-concept:C1553879,
umls-concept:C1709915,
umls-concept:C2603343,
umls-concept:C2936292
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pubmed:issue |
31
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pubmed:dateCreated |
2010-11-24
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pubmed:abstractText |
A hydrophilic interaction high-performance liquid chromatography coupled with tandem mass spectrometry method for determination of N-methyl-2-pyrrolidinone in swine liver was developed and validated. After the fortification of N-methyl-d(3)-2-pyrrolidinone-d(6) as the deuterium-labeled internal standard, N-methyl-2-pyrrolidinone in swine liver was extracted by acetonitrile and the supernatant was led through a C18+WAX mixed-mode SPE cartridge for removal of the matrix interferences. The final eluate was acidified by formic acid and then injected onto a 3?m 15cm×2.1mm TX column for hydrophilic interaction chromatographic analysis. Mass spectrometry detection was carried on a PE Sciex API 4000 triple quadrupole mass spectrometer using positive turbo-ion spray ionization mode. The MRM transitions were 100?58 for N-methyl-2-pyrrolidinone and 109?62 for N-methyl-d(3)-2-pyrrolidinone-d(6). Solvent calibration standards could be readily used for quantitative analysis of N-methyl-2-pyrrolidinone with excellent precision and accuracy, although there are endogenous levels of N-methyl-2-pyrrolidinone in many blank matrices. The true recovery was nearly 100% and the MRM signal of N-methyl-2-pyrrolidinone was suppressed about 30% because of the matrix effect. Nevertheless, N-methyl-d(3)-2-pyrrolidinone-d(6) completely compensated the ion-suppression effect and the injection-to-injection variation. The detection limit was 5ngg(-1) swine liver. The validated method was applied to a depletion study of N-methyl-2-pyrrolidinone in swine liver following intramuscular administration of a drug N-methyl-2-pyrrolidinone formulation.
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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/Acetonitriles,
http://linkedlifedata.com/resource/pubmed/chemical/Deuterium,
http://linkedlifedata.com/resource/pubmed/chemical/N-methylpyrrolidone,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrrolidinones,
http://linkedlifedata.com/resource/pubmed/chemical/acetonitrile
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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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 |
1
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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 |
3283-9
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pubmed:meshHeading |
pubmed-meshheading:21036678-Acetonitriles,
pubmed-meshheading:21036678-Animals,
pubmed-meshheading:21036678-Chromatography, High Pressure Liquid,
pubmed-meshheading:21036678-Deuterium,
pubmed-meshheading:21036678-Hydrophobic and Hydrophilic Interactions,
pubmed-meshheading:21036678-Injections, Intramuscular,
pubmed-meshheading:21036678-Liver,
pubmed-meshheading:21036678-Pyrrolidinones,
pubmed-meshheading:21036678-Reproducibility of Results,
pubmed-meshheading:21036678-Sensitivity and Specificity,
pubmed-meshheading:21036678-Swine,
pubmed-meshheading:21036678-Tandem Mass Spectrometry
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pubmed:year |
2010
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pubmed:articleTitle |
Validated hydrophilic interaction LC-MS/MS method for determination of N-methyl-2-pyrrolidinone residue: Applied to a depletion study of N-methyl-2-pyrrolidinone in swine liver following intramuscular administration of drug N-methyl-2-pyrrolidinone formulation.
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pubmed:affiliation |
State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Animal Virology of Ministry of Agriculture, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, PR China. liuyh@gsstc.gov.cn
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pubmed:publicationType |
Journal Article
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