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A methodological investigation on the estimation of the S-mephenytoin hydroxylation phenotype using the urinary S/R ratio.

作者信息

Tybring G, Bertilsson L

机构信息

Department of Clinical Pharmacology, Karolinska Institute, Huddinge University Hospital, Sweden.

出版信息

Pharmacogenetics. 1992 Oct;2(5):241-3. doi: 10.1097/00008571-199210000-00007.

DOI:10.1097/00008571-199210000-00007
PMID:1306124
Abstract

After a single oral dose of racemic mephenytoin the S/R ratio in urine can be used to phenotype extensive (EM) and poor metabolizers (PM) of S-mephenytoin. We confirmed the increased S/R ratio by storage time in EM because of the hydrolysis of a conjugate of S-mephenytoin excreted in EM, but not in PM. The S/R ratio in the 0-8 h urine increased 8- to 127-fold (from 0.22 +/- 0.16 to 9.9 +/- 11.3) after acid treatment of urine from 30 EM, but there was no effect of acid in that of 12 PM. We suggest that the phenotype of mephenytoin in combination with debrisoquine can be determined in the 0-8 h urine by estimating the mephenytoin S/R ratio before and after acid treatment.

摘要

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