Source:http://linkedlifedata.com/resource/pubmed/id/17339138
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rdf:type | |
lifeskim:mentions |
umls-concept:C0028066,
umls-concept:C0032105,
umls-concept:C0037813,
umls-concept:C0086418,
umls-concept:C0185125,
umls-concept:C0205210,
umls-concept:C0302908,
umls-concept:C0439831,
umls-concept:C0521115,
umls-concept:C0680730,
umls-concept:C0764482,
umls-concept:C1148554,
umls-concept:C1257749,
umls-concept:C2603343
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pubmed:issue |
1-2
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pubmed:dateCreated |
2007-6-4
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pubmed:abstractText |
Nifedipine (NIF), a calcium channel antagonist, is metabolized primarily by cytochrome P450 (CYP3A4) to dehydronifedipine (DNIF). As such, NIF is often used as a probe drug for determining CYP3A4 activity in human studies. A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was developed and validated to simultaneously determine NIF and DNIF in human plasma using nitrendipine as the internal standard (IS). After extraction of the plasma samples by ether-n-hexane (3:1, v/v), NIF, DNIF and the IS were subjected to LC/MS/MS analysis using electro-spray ionization (ESI). Chromatographic separation was performed on a Hypersil BDS C(18) column (50 mm x 2.1 mm, i.d., 3 microm). The method had a chromatographic running time of approximately 2.5 min and linear calibration curves over the concentrations of 0.5-100 ng/mL for NIF and DNIF. The recoveries of the one-step liquid extraction method were 81.3-89.1% for NIF and 71.6-80.4% for DNIF. The lower limit of quantification (LLOQ) of the analytical method was 0.5 ng/mL for both analytes. The intra- and inter-day precision was less than 15% for all quality control samples at concentrations of 2, 10, and 50 ng/mL. The validated LC/MS/MS method has been successfully used to study pharmacokinetic interactions of NIF with the herbal antidepressant St. John's wort in healthy volunteers. These results indicated that the developed LC/MS/MS method was efficient with a significantly shorter running time (2.5 min) for NIF and DNIF compared to those methods previously reported in the literature. The presented LC/MS/MS method had acceptable accuracy, precision and sensitivity and was used in a clinical pharmacokinetic interaction study of NIF with St. John's wort, a known herbal inducer of CYP3A4. St. John's wort was shown to induce NIF metabolism with increased plasma concentrations of DNIF.
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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 |
Jun
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pubmed:issn |
1570-0232
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
852
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
534-44
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pubmed:meshHeading |
pubmed-meshheading:17339138-Calcium Channel Blockers,
pubmed-meshheading:17339138-Drug Interactions,
pubmed-meshheading:17339138-Humans,
pubmed-meshheading:17339138-Hypericum,
pubmed-meshheading:17339138-Nifedipine,
pubmed-meshheading:17339138-Reference Standards,
pubmed-meshheading:17339138-Reproducibility of Results,
pubmed-meshheading:17339138-Sensitivity and Specificity,
pubmed-meshheading:17339138-Spectrometry, Mass, Electrospray Ionization,
pubmed-meshheading:17339138-Tandem Mass Spectrometry
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pubmed:year |
2007
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pubmed:articleTitle |
Rapid and simultaneous determination of nifedipine and dehydronifedipine in human plasma by liquid chromatography-tandem mass spectrometry: Application to a clinical herb-drug interaction study.
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pubmed:affiliation |
Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Validation Studies
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