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用于测定CYP2D6活性的新型单点血浆或唾液右美沙芬方法。

Novel single-point plasma or saliva dextromethorphan method for determining CYP2D6 activity.

作者信息

Hu O Y, Tang H S, Lane H Y, Chang W H, Hu T M

机构信息

Pharmaceutical Research Institute and School of Pharmacy, Taipei and Laboratory of Biological Psychiatry, Taipei City Psychiatric Center, Taipei, Taiwan, Republic of China.

出版信息

J Pharmacol Exp Ther. 1998 Jun;285(3):955-60.

PMID:9618394
Abstract

O-Demethylation of dextromethorphan co-segregates with 4-hydroxylation of debrisoquin and is used for CYP2D6 phenotyping. In most previous studies, 8-h urinary samples were collected for determining the dextromethorphan metabolic ratio (dextromethorphan/dextrorphan molar ratio). In addition, a salivary sampling at 3 h had been suggested for the phenotyping. To evaluate the repeatability and validity of previously reported and other potential phenotyping methods, we determined the metabolic ratios from urine samples (for various intervals), or from plasma or saliva (at varying time points) after repetitive single doses of immediate-release or repetitive multiple doses of controlled-release dextromethorphan preparations. For the single-dose study, each of 12 subjects received 15 mg of immediate-release dextromethorphan in period I and period II, respectively, with a 1-week washout period. For the multiple-dose study, each of 16 subjects received 60 mg controlled-release dextromethorphan twice daily for 5 days in period I and period II, respectively, with a 2-week washout period. Dextromethorphan and dextrorphan were assayed by high-performance liquid chromatography. In the single-dose study, most metabolic ratios revealed good repeatabilities for the two periods (paired t test). The metabolic ratio from urine collected for 4 h, 6 h, 8 h or 12 h from plasma at any time between 1 h and 5 h or at 8 h, or from saliva at 2 h or 6 h, could reflect that from 0- to 24-h urine or AUCinfinity. In the multiple-dose study, all metabolic ratios revealed good repeatabilities. The plasma metabolic ratio at any time between 0.5 h and 10 h or the saliva metabolic ratio at any time between 3 h and 12 h, but not the urine metabolic ratio from any interval, could predict the metabolic ratio from ACUSStau. The 2 h, 3 h, 4 h or 5 h plasma metabolic ratio and 6 h saliva metabolic ratios after a single dose correlated significantly with their corresponding multiple-dose metabolic ratio (r > 0.8, P < .05). In conclusion, the plasma sample at 2 h, 3 h, 4 h or 5 h or the saliva sample at 6 h in either the single immediate-release (15 mg) or the multiple controlled-release dose (60 mg) procedure could be used for determining the dextromethorphan metabolic ratio.

摘要

右美沙芬的O-去甲基化与异喹胍的4-羟化共同分离,用于CYP2D6表型分析。在大多数先前的研究中,收集8小时尿液样本以测定右美沙芬代谢率(右美沙芬/右啡烷摩尔比)。此外,有人建议在3小时时采集唾液样本进行表型分析。为了评估先前报道的和其他潜在表型分析方法的重复性和有效性,我们在重复单次剂量的速释或重复多次剂量的控释右美沙芬制剂后,测定了不同时间段尿液样本、或不同时间点血浆或唾液样本的代谢率。在单剂量研究中,12名受试者在第I期和第II期分别接受15mg速释右美沙芬,洗脱期为1周。在多剂量研究中,16名受试者在第I期和第II期分别每天两次接受60mg控释右美沙芬,共5天,洗脱期为2周。采用高效液相色谱法测定右美沙芬和右啡烷。在单剂量研究中,大多数代谢率在两个时期显示出良好的重复性(配对t检验)。在1小时至5小时之间的任何时间或8小时时采集的血浆中4小时、6小时、8小时或12小时尿液样本,或2小时或6小时唾液样本的代谢率,可反映0至24小时尿液或AUC无穷大的代谢率。在多剂量研究中,所有代谢率均显示出良好的重复性。0.5小时至10小时之间任何时间的血浆代谢率或3小时至12小时之间任何时间的唾液代谢率,但不是任何时间段的尿液代谢率,可预测ACUSStau的代谢率。单剂量后2小时、3小时、4小时或5小时的血浆代谢率和6小时的唾液代谢率与其相应的多剂量代谢率显著相关(r>0.8,P<0.05)。总之,在单次速释(15mg)或多次控释剂量(60mg)程序中,2小时、3小时、4小时或5小时的血浆样本或6小时的唾液样本可用于测定右美沙芬代谢率。

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