Source:http://linkedlifedata.com/resource/pubmed/id/17803058
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2007-9-6
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pubmed:abstractText |
A rapid and validated liquid chromatography coupled to tandem mass spectrometric method (LC-MS-MS) has been developed and applied to pharmacokinetic and bioequivalence studies in 24 healthy male Korean volunteers. The procedure involves a liquid-liquid extraction of paroxetine (CAS 61869-08-7) and fluoxetine (internal standard, CAS 54910-89-3) with ether/methyl chloride (7:3, v/v) and separated by LC equipped with C18 column using acetonitrile: 5 mmol/L ammonium formate (4:3, v/v) as mobile phase. Detection is carried out on an API 2000 MS system by multiple reactions monitoring mode. The ionization was optimized using ESI(+) and selectivity was achieved by MS-MS analysis, mlz 330.0-->192.0 and m/ z 310-->148 for paroxetine and fluoxetine, respectively. The method has a total run time of 1.5 min and was linear over a working range of 0.05-20 ng/mL and the lower limit of quantification was 0.05 ng/ mL. No endogenous compounds were found to interfere with the analysis. The inter-day and intra-day accuracy was in the ranges of 102.69-107.79% and 102.07-109.57%, respectively and precision of inter-day and intra-day expressed as relative standard deviation were 1.86-9.99% and 1.52-6.28%, respectively. The validation of this method on linearity, specificity, accuracy, precision as well as applicability to pharmacokinetic and bioequivalence studies by analysis of blood samples taken up to 72 h after oral administration of 20 mg of paroxetine in 24 healthy volunteers were found to be good performance.
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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:issn |
0004-4172
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pubmed:author |
pubmed-author:HurYeonY,
pubmed-author:JeonYong CheolYC,
pubmed-author:JheeOk HwaOH,
pubmed-author:KangJu SeopJS,
pubmed-author:KimKwang-HyunKH,
pubmed-author:LeeHeon-SooHS,
pubmed-author:LeeMin HoMH,
pubmed-author:LeeSeo EunSE,
pubmed-author:LeeSeung HoonSH,
pubmed-author:SeoHee KyoungHK,
pubmed-author:ShawLeslie MLM
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pubmed:issnType |
Print
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
455-61
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pubmed:meshHeading |
pubmed-meshheading:17803058-Antidepressive Agents, Second-Generation,
pubmed-meshheading:17803058-Area Under Curve,
pubmed-meshheading:17803058-Calibration,
pubmed-meshheading:17803058-Chromatography, High Pressure Liquid,
pubmed-meshheading:17803058-Chromatography, Liquid,
pubmed-meshheading:17803058-Cross-Over Studies,
pubmed-meshheading:17803058-Humans,
pubmed-meshheading:17803058-Paroxetine,
pubmed-meshheading:17803058-Reference Standards,
pubmed-meshheading:17803058-Reproducibility of Results,
pubmed-meshheading:17803058-Solutions,
pubmed-meshheading:17803058-Tablets,
pubmed-meshheading:17803058-Tandem Mass Spectrometry,
pubmed-meshheading:17803058-Therapeutic Equivalency
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pubmed:year |
2007
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pubmed:articleTitle |
Determination of paroxetine in plasma by liquid chromatography coupled to tandem mass spectrometry for pharmacokinetic and bioequivalence studies.
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pubmed:affiliation |
Department of Practical Arts Education, Gongju National University of Education, Gongju, Chungnam, South Korea.
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pubmed:publicationType |
Journal Article,
Randomized Controlled Trial
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