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兔眼环孢素药代动力学的房室模型

A compartmental model for the ocular pharmacokinetics of cyclosporine in rabbits.

作者信息

Oh C, Saville B A, Cheng Y L, Rootman D S

机构信息

Department of Chemical Engineering and Applied Chemistry, University of Toronto, Ontario, Canada.

出版信息

Pharm Res. 1995 Mar;12(3):433-7. doi: 10.1023/a:1016268922035.

Abstract

Studies were conducted in rabbits to determine the ocular distribution and elimination of cyclosporine, with the objective of developing a comprehensive pharmacokinetic model. Following a bolus dose into the anterior chamber, drug levels were measured in the aqueous humor, cornea, iris/ciliary body, lens, sclera, and conjunctiva. Cyclosporine was rapidly eliminated from the aqueous, but drug levels in ocular tissues persisted for in excess of 48 hours, particularly in the cornea and iris/ciliary body. The terminal elimination half life from these tissues was 45 hr and 30 hr, respectively, providing evidence that these tissues could act as a reservoir for the drug. It was found that a compartmental model accurately described the experimental data. A single compartment was used for each of the tissues and fluids sampled, except for the cornea, which was subdivided into two compartments, representing its tissue and aqueous regions.

摘要

为了建立一个全面的药代动力学模型,对兔子进行了研究,以确定环孢素在眼部的分布和消除情况。在前房给予一次大剂量药物后,测量了房水、角膜、虹膜/睫状体、晶状体、巩膜和结膜中的药物水平。环孢素迅速从房水中消除,但眼部组织中的药物水平持续超过48小时,特别是在角膜和虹膜/睫状体中。这些组织的终末消除半衰期分别为45小时和30小时,这表明这些组织可以作为药物的储存库。研究发现,房室模型能够准确描述实验数据。除角膜外,对每个采样的组织和液体都使用一个房室,角膜被细分为两个房室,分别代表其组织和房水区域。

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