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环孢素的药代动力学及血药浓度监测。

Cyclosporine pharmacokinetics and blood level monitoring.

作者信息

Burkle W S

出版信息

Drug Intell Clin Pharm. 1985 Feb;19(2):101-5. doi: 10.1177/106002808501900203.

Abstract

Although monitoring plasma or whole blood concentrations of cyclosporine has been promoted as a means of limiting toxicity while ensuring adequate immunosuppression, no consensus has been reached with regard to the assay, the specimen to be assayed, the frequency of monitoring, the therapeutic range, or even the necessity of monitoring cyclosporine concentrations. The failure to reach such a consensus can be attributed to a great extent to the complex pharmacokinetic profile of cyclosporine and the inconsistencies in the assay methodology and results used to generate is pharmacokinetic profile. This article places the subject of monitoring cyclosporine concentrations in perspective by reviewing the pharmacokinetics of cyclosporine, the assay methodology, and the published clinical experience with blood level monitoring.

摘要

尽管监测环孢素的血浆或全血浓度已被倡导为一种在确保充分免疫抑制的同时限制毒性的方法,但在检测方法、待检测标本、监测频率、治疗范围,甚至监测环孢素浓度的必要性等方面尚未达成共识。未能达成这样的共识在很大程度上可归因于环孢素复杂的药代动力学特征以及用于生成其药代动力学特征的检测方法和结果的不一致性。本文通过回顾环孢素的药代动力学、检测方法以及已发表的血药浓度监测临床经验,对监测环孢素浓度这一主题进行了全面阐述。

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