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UV spectrophotometric method for determination of phenacetin in biological specimens

Identifieur interne : 003A90 ( Main/Exploration ); précédent : 003A89; suivant : 003A91

UV 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 :

RBID : ISTEX:B84F057C704B92267D7F13AC148CC9326E429575

English descriptors

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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<term>Cobaltic</term>
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<term>Hydroxide</term>
<term>Maximum absorbance</term>
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<term>Sodium chloride</term>
<term>Sodium hydroxide</term>
<term>Sodium hydroxide solution</term>
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<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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