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哌替啶与分离出的α1-酸性糖蛋白及白蛋白的结合。

Meperidine binding to isolated alpha 1-acid glycoprotein and albumin.

作者信息

Julius H C, Levine H L, Williams W D

机构信息

Department of Pharmacy Services, Harbor-UCLA Medical Center, Torrance 90509.

出版信息

DICP. 1989 Jul-Aug;23(7-8):568-72. doi: 10.1177/1060028089023007-807.

Abstract

Interpatient variability in response to a given dose of meperidine, a synthetic opiate analgesic, may be partially explained by variability in plasma protein binding. Alpha 1-acid glycoprotein (AAG), a plasma protein that primarily binds basic drugs, has been shown to increase in patients during stress such as trauma or surgery. The objective of this study was to determine the extent of meperidine binding to AAG and albumin as a function of both protein and meperidine concentrations. We performed a simple extraction procedure and a highly sensitive gas chromatograph analytical procedure. The results indicated that meperidine binding did not vary significantly with meperidine concentration at a given AAG concentration. However, meperidine binding increased significantly (p less than 0.01) as AAG concentration increased. Conversely, meperidine binding to albumin appeared to be independent of concentration of either meperidine or albumin. In conclusion, alpha 1-acid glycoprotein is a major plasma protein which binds meperidine in patients during stress. Further studies are suggested to elucidate the role of AAG on the pharmacologic effects of meperidine.

摘要

对于给定剂量的合成阿片类镇痛药哌替啶,患者间的反应差异可能部分归因于血浆蛋白结合的差异。α1-酸性糖蛋白(AAG)是一种主要结合碱性药物的血浆蛋白,在创伤或手术等应激状态下,患者体内的AAG会升高。本研究的目的是确定哌替啶与AAG和白蛋白的结合程度与蛋白及哌替啶浓度的关系。我们采用了简单的萃取程序和高灵敏度的气相色谱分析程序。结果表明,在给定的AAG浓度下,哌替啶结合率不会随哌替啶浓度的变化而显著改变。然而,随着AAG浓度升高,哌替啶结合率显著增加(p<0.01)。相反,哌替啶与白蛋白的结合似乎与哌替啶或白蛋白的浓度无关。总之,α1-酸性糖蛋白是应激状态下患者体内结合哌替啶的主要血浆蛋白。建议开展进一步研究以阐明AAG在哌替啶药理作用中的作用。

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