• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

线性药代动力学的一般处理方法。

General treatment of linear pharmacokinetics.

作者信息

Pedersen P V

出版信息

J Pharm Sci. 1978 Feb;67(2):187-91. doi: 10.1002/jps.2600670216.

DOI:10.1002/jps.2600670216
PMID:621634
Abstract

A general treatment of linear pharmacokinetics that enables equations to be obtained simply for all linear compartmental models, with input in one or more compartments, is presented. Two approaches are described: one based on a full Laplace transformation and one that avoids transformation of the input functions and the use of convolution integrals. The latter approach is of particular interest when dealing with complex input functions not having a simple Laplace transform. The concept of acceptor and donor subsystems is introduced. It is demonstrated that disposition in certain models may be simplified and analyzed in terms of disposition in subsystems of simpler composition. The treatment presented is illustrated with several examples.

摘要

本文提出了一种线性药代动力学的通用处理方法,该方法能够简单地获得适用于所有线性房室模型的方程,这些模型的输入可以在一个或多个房室中。文中描述了两种方法:一种基于完全拉普拉斯变换,另一种则避免了输入函数的变换以及卷积积分的使用。当处理没有简单拉普拉斯变换的复杂输入函数时,后一种方法特别有用。文中引入了受体和供体子系统的概念。结果表明,某些模型中的处置情况可以根据组成更简单的子系统中的处置情况进行简化和分析。文中通过几个例子说明了所提出的处理方法。

相似文献

1
General treatment of linear pharmacokinetics.线性药代动力学的一般处理方法。
J Pharm Sci. 1978 Feb;67(2):187-91. doi: 10.1002/jps.2600670216.
2
Derivation of Laplace transform for the general disposition deconvolution equation in drug metabolism kinetics.药物代谢动力学中一般处置反卷积方程的拉普拉斯变换推导。
Exp Toxicol Pathol. 1999 Jul;51(4-5):409-11. doi: 10.1016/S0940-2993(99)80030-X.
3
General pharmacokinetic equations for linear mammillary models with drug absorption into peripheral compartments.具有药物吸收进入外周室的线性乳头状模型的一般药代动力学方程。
Eur J Clin Pharmacol. 1975 Feb 28;8(2):141-8. doi: 10.1007/BF00561564.
4
[Model building in pharmacokinetics/Part II: Generalized theoretical presentation of complete integration of linear compartment models of optional structure (author's transl)].[药代动力学中的模型构建/第二部分:可选结构线性房室模型完全整合的广义理论阐述(作者译)]
Arzneimittelforschung. 1977;27(4a):900-4.
5
The deterministic identifiability of nonlinear pharmacokinetic models.非线性药代动力学模型的确定性可识别性
J Pharmacokinet Biopharm. 1984 Apr;12(2):177-91. doi: 10.1007/BF01059277.
6
[Model building in pharmacokinetics/Part III: Simplified rules for the deduction of analytical solutions for linear compartment models (author's transl)].[药代动力学中的模型构建/第三部分:线性房室模型解析解推导的简化规则(作者译)]
Arzneimittelforschung. 1977;27(4a):904-11.
7
An integrated approach to pharmacokinetic analysis for linear mammillary systems in which input and exit may occur in/from any compartment.一种针对线性乳腺系统的药代动力学分析的综合方法,其中输入和输出可能发生在任何隔室中/从任何隔室输出。
J Pharmacokinet Biopharm. 1989 Dec;17(6):673-86. doi: 10.1007/BF01062124.
8
Model-independent method of analyzing input in linear pharmacokinetic systems having polyexponential impulse response I: Theoretical analysis.具有多指数脉冲响应的线性药代动力学系统中输入分析的非模型依赖方法I:理论分析
J Pharm Sci. 1980 Mar;69(3):298-305. doi: 10.1002/jps.2600690314.
9
Physicochemical interpretation of the pharmacokinetics of percutaneous absorption.经皮吸收药代动力学的物理化学解释
J Pharmacokinet Biopharm. 1983 Apr;11(2):189-203. doi: 10.1007/BF01061849.
10
Derivation and presentation of formulas for drug concentrations in two-, three- and four-compartment pharmacokinetic models.二室、三室和四室药代动力学模型中药物浓度公式的推导与呈现。
J Pharmacol Toxicol Methods. 2019 Nov-Dec;100:106621. doi: 10.1016/j.vascn.2019.106621. Epub 2019 Jul 26.

引用本文的文献

1
Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration.用于预测亲脂性药物口服给药后血浆特征的生物相关性溶出度测试。
Pharm Res. 2001 Mar;18(3):380-8. doi: 10.1023/a:1011071401306.
2
Chemical substance kinetics in the case of chronobiological variations of elimination rate.消除速率发生生物钟学变化时的化学物质动力学
Eur J Drug Metab Pharmacokinet. 1999 Oct-Dec;24(4):293-7. doi: 10.1007/BF03190035.
3
An approach for determination of chronopharmacokinetic parameters of methotrexate.一种测定甲氨蝶呤时辰药代动力学参数的方法。
Eur J Drug Metab Pharmacokinet. 1997 Jan-Mar;22(1):41-5. doi: 10.1007/BF03189783.
4
Theorems and implications of a model independent elimination/distribution function decomposition of linear and some nonlinear drug dispositions. I. Derivations and theoretical analysis.线性及部分非线性药物处置的模型无关消除/分布函数分解的定理与推论。I. 推导与理论分析。
J Pharmacokinet Biopharm. 1984 Dec;12(6):627-48. doi: 10.1007/BF01059557.
5
Linear and nonlinear system approaches in pharmacokinetics: how much do they have to offer? II. The response mapping operator (RMO) approach.药代动力学中的线性和非线性系统方法:它们能提供多少价值?II. 响应映射算子(RMO)方法。
J Pharmacokinet Biopharm. 1988 Oct;16(5):543-71. doi: 10.1007/BF01062384.
6
Mean time parameters in pharmacokinetics. Definition, computation and clinical implications (Part II).药代动力学中的平均时间参数。定义、计算及临床意义(第二部分)
Clin Pharmacokinet. 1989 Dec;17(6):424-40. doi: 10.2165/00003088-198917060-00005.
7
Pharmacokinetics of haemoperfusion for drug overdose.药物过量血液灌流的药代动力学
Clin Pharmacokinet. 1979 Sep-Oct;4(5):329-54. doi: 10.2165/00003088-197904050-00001.