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华法林对映体的药代动力学:寻找个体内相关性。

Pharmacokinetics of warfarin enantiomers: a search for intrasubject correlations.

作者信息

Wingard L B, O'Reilly R A, Levy G

出版信息

Clin Pharmacol Ther. 1978 Feb;23(2):212-7. doi: 10.1002/cpt1978232212.

Abstract

The total body clearance of single doses of R(+)-, S(-)-, and racemic warfarin and the plasma concentration-anticoagulant effect curves for these drugs were determined in 10 healthy men, 21 to 51 yr old. This information was used to calculate the steady-state dose required to decrease prothrombin complex activity to about 30% of normal. This dose (mean +/- SD in mg/70 kg/day) is 17.8 +/- 9.3 for R(+)-warfarin, 6.63 +/- 2.19 for S(-)-warfarin, and 9.4 +/- 1.7 for racemic warfarin. There is a correlation between the maintenance doses of racemic and S(-)-warfarin (r = 0.89, p less than 0.01) but not between those of racemic and R(+)-warfarin (r = 0.30, NS). According to these calculations, the maintenance dose of racemic warfarin required by an individual patient may be a useful predictor of maintenance dose of S(-)-warfarin which will produce a comparable degree of anticoagulation. No such predictability is evident with respect to R(+)-warfarin. The slopes of the log plasma concentration-anticoagulant effect curves for R(+)-and S(-)-warfarin differ significantly. Therefore, the potency ratio of these enantiomers is dose-and concentration-dependent.

摘要

在10名年龄为21至51岁的健康男性中,测定了单剂量R(+)-、S(-)-和消旋华法林的全身清除率以及这些药物的血浆浓度-抗凝效应曲线。利用这些信息计算出使凝血酶原复合物活性降至正常水平约30%所需的稳态剂量。该剂量(以mg/70 kg/天计,均值±标准差),R(+)-华法林为17.8±9.3,S(-)-华法林为6.63±2.19,消旋华法林为9.4±1.7。消旋华法林与S(-)-华法林的维持剂量之间存在相关性(r = 0.89,p<0.01),但消旋华法林与R(+)-华法林的维持剂量之间不存在相关性(r = 0.30,无显著性差异)。根据这些计算结果,个体患者所需的消旋华法林维持剂量可能是产生相当抗凝程度的S(-)-华法林维持剂量的有用预测指标。对于R(+)-华法林,不存在这种可预测性。R(+)-和S(-)-华法林的对数血浆浓度-抗凝效应曲线斜率有显著差异。因此,这些对映体的效价比是剂量和浓度依赖性的。

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