Comparison of two and three compartment models of phencyclidine in man.

Substance and alcohol actions/misuse Pub Date : 1982-01-01
S E Domino, L E Domino, E F Domino
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Abstract

A pharmacokinetic analysis comparing a 2 and 3 compartment model was performed on the published data of Wall et al. (12) on the kinetics of phencyclidine (PCP). These investigators gave 100 micrograms (mean 1.3 micrograms/kg) of 3H-PCP i.v. to three human volunteers and followed the plasma disappearance of PCP over 72 hr. They suggested that PCP followed a 2 compartment model with a plasma half life of 7-16 hr. In the present analysis, additional pharmacokinetic estimations from the plasma data were made and a 3 compartment model developed. The results obtained suggest complex PCP kinetics involving an initial pi half life of 5.5 min, an alpha half life of 4.6 hr, and a beta half life of 22 hr. The volume of distribution was large, varying from 2.2 to 2.4 1/kg for each compartment, suggesting binding of PCP.

苯环利定在人体内二室和三室模型的比较。
根据Wall等人(12)发表的关于苯环利定(PCP)动力学的数据,对2室和3室模型进行了药代动力学分析。这些研究人员给3名志愿者静脉注射100微克(平均1.3微克/公斤)的3H-PCP,并在72小时内观察PCP血浆消失情况。他们建议PCP遵循2室模型,血浆半衰期为7-16小时。在本分析中,根据血浆数据进行了额外的药代动力学估计,并建立了3室模型。得到的结果表明,复杂的PCP动力学涉及初始pi半衰期5.5分钟,α半衰期4.6小时,β半衰期22小时。分布体积大,每隔室2.2 ~ 2.4个/kg,提示PCP结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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