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甲苯磺丁脲慢代谢者的筛查试验。

A screening test for slow metabolisers of tolbutamide.

作者信息

Page M A, Boutagy J S, Shenfield G M

机构信息

Department of Clinical Pharmacology, Royal North Shore Hospital, NSW, Australia.

出版信息

Br J Clin Pharmacol. 1991 Jun;31(6):649-54. doi: 10.1111/j.1365-2125.1991.tb05587.x.

Abstract
  1. Six subjects participated in a detailed pharmacokinetic study of tolbutamide (pilot study). Using parameters based on these data, sixty-three non-diabetic volunteers underwent a simple screening test designed to identify slow metabolisers of tolbutamide. 2. The screening test was an estimate of tolbutamide plasma elimination half-life from plasma concentrations at 8 and 24 h after 500 mg tolbutamide orally, and urinary recovery of the hydroxy- and carboxytolbutamide metabolites over the 4-8 h post-dose period. 3. The mean tolbutamide half-life for 61 of the screened subjects was 7.5 +/- 1.5 h (range 5.2-12.2 h). Two subjects had half-lives of 21.6 and 16.1 h. Their urinary metabolite recoveries were within the range of those in the screening test but lower than those in the pilot study. 4. The subject with the 21.6 h half-life was restudied with intensive serial sampling for 72 h post-dose. She was confirmed as a 'slow' metaboliser of tolbutamide since her terminal half-life was 25.9 h but plasma Cmax and tmax were within the range of those in the detailed study. This subject's 24 h urinary recoveries of both hydroxytolbutamide and carboxytolbutamide were clearly different from the mean values for the pilot study subjects implicating hydroxylation of tolbutamide as the metabolic defect. 5. The two point plasma half-life is therefore a discriminatory screening test but a 4-8 h urinary recovery is not. 6. A partial family study did not provide conclusive evidence of the inheritance of slow tolbutamide metabolism but the screening test should allow simple identification of slow metabolisers for further study.
摘要
  1. 六名受试者参与了甲苯磺丁脲的详细药代动力学研究(初步研究)。基于这些数据得出参数,63名非糖尿病志愿者接受了一项简单的筛查试验,旨在识别甲苯磺丁脲的慢代谢者。2. 筛查试验是根据口服500mg甲苯磺丁脲后8小时和24小时的血浆浓度估算甲苯磺丁脲的血浆消除半衰期,以及给药后4 - 8小时内羟基甲苯磺丁脲和羧基甲苯磺丁脲代谢物的尿回收率。3. 61名经筛查受试者的甲苯磺丁脲平均半衰期为7.5±1.5小时(范围5.2 - 12.2小时)。两名受试者的半衰期分别为21.6小时和16.1小时。他们的尿代谢物回收率在筛查试验范围内,但低于初步研究中的回收率。4. 对半衰期为21.6小时的受试者在给药后进行了72小时的密集连续采样重新研究。她被确认为甲苯磺丁脲的“慢”代谢者,因为其终末半衰期为25.9小时,但血浆Cmax和tmax在详细研究范围内。该受试者24小时尿中羟基甲苯磺丁脲和羧基甲苯磺丁脲的回收率与初步研究受试者的平均值明显不同,提示甲苯磺丁脲的羟基化是代谢缺陷。5. 因此,两点血浆半衰期是一种有鉴别力的筛查试验,但4 - 8小时尿回收率不是。6. 一项部分家系研究未提供甲苯磺丁脲慢代谢遗传的确凿证据,但筛查试验应能简单识别慢代谢者以便进一步研究。

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A screening test for slow metabolisers of tolbutamide.甲苯磺丁脲慢代谢者的筛查试验。
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Pharmacokinetics of tolbutamide in ethnic Chinese.甲苯磺丁脲在中国汉族人群中的药代动力学。
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