Abstract
Six slow acetylators (SAs) and six rapid acetylators (RAs), as determined by sulfamethazine (SMZ) phenotyping, were each given a 2-mg oral dose of clonazepam. Ninety-six-hour urine collections from these subjects were analyzed for clonazepam, 7-amino clonazepam (7-AM, clonazepam nitroreduced metabolite), and 7-acetamido clonazepam (7-ACT, N -acetylated 7-AM). The SA group excreted more 7-AM and less 7-ACT than the RA group; mean (±SD) recovered as 7-AM was 22.7 ± 5.0% for the SA group and 13.6 ± 4.1% for the RA group and mean (±SD) recovered as 7-ACT was 1.5 ± 0.4% for the SA group and 3.9 ± 1.8% for the RA group. Both differences were substantial (p < 0.02 by unpaired t test) and indicate that the rate of acetylation of 7-AM to 7-ACT in the biotransformation of clonazepam is determined by the acetylator phenotype.
Original language | American English |
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Journal | Clinical Pharmacology & Therapeutics |
Volume | 30 |
DOIs | |
State | Published - Sep 1 1981 |
Disciplines
- Medical Specialties
- Medicine and Health Sciences
- Pediatrics