Source:http://linkedlifedata.com/resource/pubmed/id/16934427
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-12-26
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pubmed:abstractText |
A sensitive and selective high-performance liquid chromatography-electrospray ionisation-tandem mass spectrometry (HPLC-ESI-MS-MS) method for determination of rosiglitazone in human plasma has been developed. After the addition of the internal standard, plasma samples were precipitated by acetonitrile. The compounds were separated on a proC18 column using a mixture of ammonium acetate buffer (0.02 M, pH 6.5) and acetonitrile (in the ratio of 47:53, v/v) as mobile phase. A Finnigan LCQdeca plus ion trap mass spectrometer connected to a Finnigan Surveyor HPLC was used to develop and validate the method. Linearity was established for the range of concentrations 1-1000 ng/ml with a coefficient of determination (r(2)) of 0.999. The intra-day accuracy for rosiglitazone ranged from 110.0 to 99.2% at low, medium and high levels. The inter-day accuracy was less than 15%. The lower limit of quantitation (LLOQ) was identified reproducible at 1.0 ng/ml with a precision of 5.7%. After validation, the method was used to study the pharmacokinetic profile of rosiglitazone in five healthy volunteers after administration of a single oral dose (4.0mg). The proposed method enabled the unambiguous evaluation and quantitation of rosiglitazone for pharmacokinetic, bioavailability or drug-drug interaction studies. A possible chromatography peak (m/z 121, its parent ion m/z 344) of N-demethyl rosiglitazone was observed at 3.49 min during determining rosiglitazone. This may be also a potential method for simultaneous determination of rosiglitazone and its metabolite N-demethyl rosiglitazone concentrations in plasma.
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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:month |
Jan
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pubmed:issn |
0731-7085
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
580-5
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pubmed:meshHeading |
pubmed-meshheading:16934427-Administration, Oral,
pubmed-meshheading:16934427-Adult,
pubmed-meshheading:16934427-Biological Availability,
pubmed-meshheading:16934427-Chromatography, High Pressure Liquid,
pubmed-meshheading:16934427-Drug Monitoring,
pubmed-meshheading:16934427-Humans,
pubmed-meshheading:16934427-Hypoglycemic Agents,
pubmed-meshheading:16934427-Male,
pubmed-meshheading:16934427-Reference Standards,
pubmed-meshheading:16934427-Reference Values,
pubmed-meshheading:16934427-Reproducibility of Results,
pubmed-meshheading:16934427-Sensitivity and Specificity,
pubmed-meshheading:16934427-Spectrometry, Mass, Electrospray Ionization,
pubmed-meshheading:16934427-Tandem Mass Spectrometry,
pubmed-meshheading:16934427-Thiazolidinediones
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pubmed:year |
2007
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pubmed:articleTitle |
Sensitive and selective liquid chromatography-mass spectrometry method for the quantification of rosiglitazone in human plasma.
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pubmed:affiliation |
Pharmacogenetics Research Institute, Institute of Clinical Pharmacology, Central South University, 110 Xiang Ya Road, Changsha, Hunan 410078, China.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Validation Studies
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