CLINICAL PHARMACOKINETICS OF PROCAINAMIDE INFUSIONS IN RELATION TO ACETYLATOR PHENOTYPE

被引:33
作者
LIMA, JJ
CONTI, DR
GOLDFARB, AL
TILSTONE, WJ
GOLDEN, LH
JUSKO, WJ
机构
[1] SUNY BUFFALO, SCH PHARM, DEPT PHARMACEUT, AMHERST, NY 14260 USA
[2] SUNY BUFFALO, SCH MED, DEPT MED, BUFFALO, NY 14214 USA
来源
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS | 1979年 / 7卷 / 01期
关键词
acetylator phenotype; constant-rate infusion; pharmacogenetics; pharmacokinetics; procainamide; renal impairment;
D O I
10.1007/BF01059442
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics of procainamide was determined in 21 lidocaine-resistant patients who received the drug according to a pharmacokinetically designed double-infusion technique. Thirteen patients were phenotyped as slow acetylators, seven as fast, and one as intermediate. The total body clearances (ClT) of PA in slow and fast acetylators were 22.6 and 34.8 liters/hr, respectively. The fraction of PA cleared by the formation of NAPA in the corresponding acetylator group was 0.2 and 0.4. Renal impairment affected the pharmacokinetics of PA more profoundly as the ClTs of PA in patients with and without renal impairment were 17.9 and 31.2 liters/hr, respectively. None of the calculated volumes of distribution was affected by acetylator phenotype or renal impairment. These data identify the contribution of at least two of the major factors accounting for variability in PA disposition in patients undergoing therapy. © 1979 Plenum Publishing Corporation.
引用
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页码:69 / 85
页数:17
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