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基于快速拉普拉斯逆变换(FILT)循环理论的药物动静脉血药浓度差分析。

Analysis of arterial-venous blood concentration difference of drugs based on recirculatory theory with fast inverse Laplace transform (FILT).

作者信息

Yano Y, Yamaoka K, Yasui H, Nakagawa T

机构信息

Faculty of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

J Pharmacokinet Biopharm. 1991 Feb;19(1):71-85. doi: 10.1007/BF01062193.

Abstract

An arterial and venous blood (or plasma) concentration difference of drugs across the lung of rats was evaluated based on the recirculatory concept. The recirculatory system is given by the combination of the transfer functions for the pulmonary and the systemic circulations and is described by a Laplace-transformed equation, i.e., an image equation. For the manipulation of the image equations, the fast inverse Laplace transform (FILT) was adopted and MULTI(FILT) was used for the simultaneous curve fitting to estimate the pharmacokinetic parameters in the recirculatory model. Metoprolol as a test drug and cephalexin as a control drug were infused respectively into the femoral vein for 30 min, and arterial and venous blood samples were collected simultaneously through the cannula at the femoral artery and at right atrium during and after the infusion. Exponential functions were assumed for the weight functions through both the pulmonary and systemic circulations. Results of the curve fitting showed that the single-pass extraction ratio through the pulmonary circulation (Ep) of metoprolol was about 0.2, whereas that of cephalexin was negligible. The mean transit times through the pulmonary circulation (tp) of metoprolol and cephalexin were both about 0.5 min, which is small. The single-pass extraction ratios through the systemic circulation (Es) of metoprolol and cephalexin were both about 0.1, and the mean transit times through the systemic circulation (ts) were 11.5 min and 8.2 min, respectively.

摘要

基于再循环概念评估了大鼠肺部药物的动静脉血(或血浆)浓度差。再循环系统由肺循环和体循环的传递函数组合给出,并由拉普拉斯变换方程描述,即像方程。为了处理像方程,采用了快速逆拉普拉斯变换(FILT),并使用MULTI(FILT)进行同时曲线拟合,以估计再循环模型中的药代动力学参数。分别将美托洛尔作为受试药物和头孢氨苄作为对照药物注入股静脉30分钟,并在输注期间和之后通过股动脉插管和右心房插管同时采集动脉和静脉血样。假设肺循环和体循环的权重函数均为指数函数。曲线拟合结果表明,美托洛尔通过肺循环的单通道提取率(Ep)约为0.2,而头孢氨苄的提取率可忽略不计。美托洛尔和头孢氨苄通过肺循环的平均转运时间(tp)均约为0.5分钟,较短。美托洛尔和头孢氨苄通过体循环的单通道提取率(Es)均约为0.1,通过体循环的平均转运时间(ts)分别为11.5分钟和8.2分钟。

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