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Microsomal prediction of in vivo clearance of CYP2C9 substrates in humans.人体中CYP2C9底物体内清除率的微粒体预测
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本文引用的文献

1
The effect of sulphinpyrazone on oxidative drug metabolism in man: inhibition of tolbutamide elimination.磺吡酮对人体氧化药物代谢的影响:对甲苯磺丁脲消除的抑制作用。
Eur J Clin Pharmacol. 1982;22(4):321-6. doi: 10.1007/BF00548400.
2
Pharmacogenetics of mephenytoin: a new drug hydroxylation polymorphism in man.美芬妥英的药物遗传学:人类一种新的药物羟基化多态性
Eur J Clin Pharmacol. 1984;26(6):753-9. doi: 10.1007/BF00541938.
3
Drug absorption, metabolism, and excretion. IX. Some new aspects of pharmacokinetics on tolbutamide in rabbits.药物吸收、代谢及排泄。IX. 家兔甲苯磺丁脲药代动力学的一些新进展。
Chem Pharm Bull (Tokyo). 1973 Aug;21(8):1754-63. doi: 10.1248/cpb.21.1754.
4
Normal metabolism of debrisoquine and theophylline in a slow tolbutamide metaboliser.在一名甲苯磺丁脲代谢缓慢者中去甲丙咪嗪和茶碱的正常代谢
Aust N Z J Med. 1985 Jun;15(3):348-9. doi: 10.1111/j.1445-5994.1985.tb04052.x.
5
Polymorphic drug oxidation: pharmacokinetic basis and comparison of experimental indices.多态性药物氧化:药代动力学基础及实验指标比较
Br J Clin Pharmacol. 1986 Nov;22(5):541-50. doi: 10.1111/j.1365-2125.1986.tb02933.x.
6
Hepatic metabolism of tolbutamide: characterization of the form of cytochrome P-450 involved in methyl hydroxylation and relationship to in vivo disposition.甲苯磺丁脲的肝脏代谢:参与甲基羟基化的细胞色素P-450形式的特征及其与体内处置的关系。
J Pharmacol Exp Ther. 1987 Jun;241(3):1112-9.
7
Lack of relationship between tolbutamide metabolism and debrisoquine oxidation phenotype.甲苯磺丁脲代谢与异喹胍氧化表型之间缺乏相关性。
Eur J Clin Pharmacol. 1987;33(4):397-402. doi: 10.1007/BF00637637.
8
Selective inhibition of drug oxidation after simultaneous administration of two probe drugs, antipyrine and tolbutamide.同时给予两种探针药物安替比林和甲苯磺丁脲后对药物氧化的选择性抑制作用。
Eur J Clin Pharmacol. 1988;34(2):157-63. doi: 10.1007/BF00614553.
9
Characterization of the common genetic defect in humans deficient in debrisoquine metabolism.异喹胍代谢缺陷人类常见遗传缺陷的特征分析。
Nature. 1988 Feb 4;331(6155):442-6. doi: 10.1038/331442a0.
10
Expression of a human liver cytochrome P-450 protein with tolbutamide hydroxylase activity in Saccharomyces cerevisiae.具有甲苯磺丁脲羟化酶活性的人肝细胞色素P-450蛋白在酿酒酵母中的表达
Biochemistry. 1989 Jun 13;28(12):4993-9. doi: 10.1021/bi00438a014.

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.

DOI:10.1111/j.1365-2125.1991.tb05587.x
PMID:1867959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1368574/
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。