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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1977-9-29
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pubmed:abstractText |
Acenocoumarol, to which a 14C-labeled internal standard has been added, is extracted at pH 4 into ethyl acetate-heptane (20:80 v/v), back-extracted into aqueous sodium hydroxide solution after solvent washing with a pH 7 buffer, and reextracted after acidification in the solvent mixture. It is then acetylated with 3H-acetic anhydride. The acenocoumarol acetyl derivative is separated from the metabolite derivatives by TLC, and its radioactivity is measured. The method is specific and sensitive to a concentration of 8 ng/ml.
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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 |
0022-3549
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
997-1000
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pubmed:dateRevised |
2000-12-18
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pubmed:meshHeading |
pubmed-meshheading:18595-Acenocoumarol,
pubmed-meshheading:18595-Acetylation,
pubmed-meshheading:18595-Carbon Radioisotopes,
pubmed-meshheading:18595-Chromatography, Thin Layer,
pubmed-meshheading:18595-Hydrogen-Ion Concentration,
pubmed-meshheading:18595-Isotope Labeling,
pubmed-meshheading:18595-Kinetics,
pubmed-meshheading:18595-Methods,
pubmed-meshheading:18595-Tritium
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pubmed:year |
1977
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pubmed:articleTitle |
Determination of acenocoumarol in plasma and urine by double radioisotope derivative analysis.
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pubmed:publicationType |
Journal Article
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