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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1989-2-22
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pubmed:abstractText |
A sensitive reversed-phase high-performance liquid chromatographic method for the determination of labetalol has been developed. A mobile phase consisting of citrate buffer (pH 6.5), acetonitrile and 2-propanol and an RP-8 column were used. The sensitivity of the fluorescence detection was enhanced to 1 ng/ml of labetalol in plasma by optimizing the emitted light. General guidelines for optimization of fluorescence detection are discussed.
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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 |
Jul
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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 |
446
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
323-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading | |
pubmed:year |
1988
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pubmed:articleTitle |
Optimization of fluorescence detection for the determination of labetalol in plasma by high-performance liquid chromatography.
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pubmed:affiliation |
Drug Research Institute, Modra, Czechoslovakia.
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pubmed:publicationType |
Journal Article
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