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蛋白质结合动力学决定药物进入大脑的摄取速率。

Kinetics of protein binding determine rates of uptake of drugs by brain.

作者信息

Robinson P J, Rapoport S I

出版信息

Am J Physiol. 1986 Dec;251(6 Pt 2):R1212-20. doi: 10.1152/ajpregu.1986.251.6.R1212.

Abstract

A mathematical model describing the kinetics of binding and release of substances by plasma proteins is presented. The effects of protein binding on the uptake of substances such as drugs from the capillary network of the brain are discussed. The model assumes equilibration between bound and free forms of drug in arterial blood and incorporates the on-off rate constants for the drug-protein complex and rate constants for passage of free drug across the blood-brain barrier and for drug metabolism in the brain. Regional cerebral blood flow and the related capillary transit time are important parameters in the model. Analytical expressions for bound and free drug concentrations and for the net extraction of drug are derived where practicable, and numerical solutions also are presented. Effects of changes in the total drug and protein concentrations in the plasma are discussed with special reference to the uptake of bilirubin by the brain.

摘要

本文提出了一个描述血浆蛋白结合和释放物质动力学的数学模型。讨论了蛋白质结合对从脑毛细血管网络摄取药物等物质的影响。该模型假设动脉血中药物的结合态和游离态之间达到平衡,并纳入了药物 - 蛋白质复合物的结合和解离速率常数,以及游离药物穿过血脑屏障的速率常数和脑中药物代谢的速率常数。局部脑血流量和相关的毛细血管通过时间是该模型中的重要参数。在可行的情况下,推导了结合态和游离态药物浓度以及药物净提取率的解析表达式,并给出了数值解。特别参考脑对胆红素的摄取,讨论了血浆中总药物浓度和蛋白质浓度变化的影响。

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