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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1992-8-14
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pubmed:abstractText |
Two methods for the determination of the enantiomeric ratio of verapamil in plasma by high-performance liquid chromatography have been developed. On an alpha 1-acid glycoprotein chiral stationary phase (Chiral-AGP) verapamil was separated after the acetylation of the main metabolite norverapamil, which interferes with the resolution of verapamil. On an amylose tris-3,5-dimethylphenylcarbamate column (Chiralpak AD) verapamil and norverapamil were determined simultaneously without prior derivatization. Gallopamil was separated on both columns under similar conditions.
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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 |
Mar
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pubmed:issn |
0021-9673
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
575
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
255-60
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1629301-Animals,
pubmed-meshheading:1629301-Chromatography, High Pressure Liquid,
pubmed-meshheading:1629301-Gallopamil,
pubmed-meshheading:1629301-Humans,
pubmed-meshheading:1629301-Male,
pubmed-meshheading:1629301-Microsomes, Liver,
pubmed-meshheading:1629301-Rats,
pubmed-meshheading:1629301-Rats, Inbred Strains,
pubmed-meshheading:1629301-Reproducibility of Results,
pubmed-meshheading:1629301-Stereoisomerism,
pubmed-meshheading:1629301-Verapamil
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pubmed:year |
1992
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pubmed:articleTitle |
Direct determination of the enantiomeric ratio of verapamil, its major metabolite norverapamil and gallopamil in plasma by chiral high-performance liquid chromatography.
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pubmed:affiliation |
Institute of Pharmaceutical Chemistry, University of Münster, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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