UV spectrophotometric method for determination of phenacetin in biological specimens
Identifieur interne : 003A90 ( Main/Exploration ); précédent : 003A89; suivant : 003A91UV spectrophotometric method for determination of phenacetin in biological specimens
Auteurs : Jack E. Wallace [États-Unis] ; John D. Biggs [États-Unis] ; Horace E. Hamilton [États-Unis] ; Lloyd L. Foster [États-Unis] ; Kenneth Blum [États-Unis]Source :
- Journal of Pharmaceutical Sciences [ 0022-3549 ] ; 1973-04.
English descriptors
- Teeft :
- Absorbance, Aerospace medicine, Axelrod, Biological specimens, Body weight, Cobaltic, Cobaltic oxide, Ether, Hydroxide, Maximum absorbance, Naoh, Oxidized, Paminophenol, Pharmacological agents, Phenacetin, Phenacetin product, Primary metabolite, Sodium chloride, Sodium hydroxide, Sodium hydroxide solution, Solvent layer, Spectrophotometric, Spectrophotometric method, Urine, Usaf school.
Abstract
A UV spectrophotometric procedure for determining phenacetin in biological specimens is described. The drug is extracted from biological material by ether and oxidized to a quinone product by cobaltic oxide. The primary metabolite of phenacetin, N‐acetyl‐p‐aminophenol, is assayed by providing a salting‐out step in the extraction process. Better than 90% of phenacetin added to urine and serum specimens in vitro at concentrations of 5–50 mcg./ml. was recovered. From homogenized tissue, 83% of added phenacetin was recovered.
Url:
DOI: 10.1002/jps.2600620411
Affiliations:
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Le document en format XML
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<series><title level="j" type="main">Journal of Pharmaceutical Sciences</title>
<title level="j" type="alt">JOURNAL OF PHARMACEUTICAL SCIENCES</title>
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<term>Axelrod</term>
<term>Biological specimens</term>
<term>Body weight</term>
<term>Cobaltic</term>
<term>Cobaltic oxide</term>
<term>Ether</term>
<term>Hydroxide</term>
<term>Maximum absorbance</term>
<term>Naoh</term>
<term>Oxidized</term>
<term>Paminophenol</term>
<term>Pharmacological agents</term>
<term>Phenacetin</term>
<term>Phenacetin product</term>
<term>Primary metabolite</term>
<term>Sodium chloride</term>
<term>Sodium hydroxide</term>
<term>Sodium hydroxide solution</term>
<term>Solvent layer</term>
<term>Spectrophotometric</term>
<term>Spectrophotometric method</term>
<term>Urine</term>
<term>Usaf school</term>
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<front><div type="abstract" xml:lang="en">A UV spectrophotometric procedure for determining phenacetin in biological specimens is described. The drug is extracted from biological material by ether and oxidized to a quinone product by cobaltic oxide. The primary metabolite of phenacetin, N‐acetyl‐p‐aminophenol, is assayed by providing a salting‐out step in the extraction process. Better than 90% of phenacetin added to urine and serum specimens in vitro at concentrations of 5–50 mcg./ml. was recovered. From homogenized tissue, 83% of added phenacetin was recovered.</div>
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<name sortKey="Biggs, John D" sort="Biggs, John D" uniqKey="Biggs J" first="John D." last="Biggs">John D. Biggs</name>
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<name sortKey="Wallace, Jack E" sort="Wallace, Jack E" uniqKey="Wallace J" first="Jack E." last="Wallace">Jack E. Wallace</name>
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