• 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

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.

DOI:10.1007/BF01062193
PMID:2023110
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。

相似文献

1
Analysis of arterial-venous blood concentration difference of drugs based on recirculatory theory with fast inverse Laplace transform (FILT).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。
J Pharmacokinet Biopharm. 1991 Feb;19(1):71-85. doi: 10.1007/BF01062193.
2
Analysis of enterohepatic circulation of cefixime in rat by fast inverse Laplace transform (FILT).通过快速拉普拉斯逆变换(FILT)分析大鼠体内头孢克肟的肠肝循环。
J Pharmacokinet Biopharm. 1990 Dec;18(6):545-59. doi: 10.1007/BF01073938.
3
A nonlinear least squares program, MULTI(FILT), based on fast inverse Laplace transform for microcomputers.一种基于快速拉普拉斯逆变换的用于微型计算机的非线性最小二乘程序MULTI(FILT)。
Chem Pharm Bull (Tokyo). 1989 Apr;37(4):1035-8. doi: 10.1248/cpb.37.1035.
4
Implementing PRED Subroutine of NONMEM for Versatile Pharmacokinetic Analysis Using Fast Inversion of Laplace Transform (FILT).使用快速拉普拉斯变换逆变换(FILT)实现 NONMEM 的 PRED 子例程进行通用药代动力学分析。
Chem Pharm Bull (Tokyo). 2020 Sep 1;68(9):891-894. doi: 10.1248/cpb.c20-00236. Epub 2020 Jul 1.
5
A recirculatory model with enterohepatic circulation by measuring portal and systemic blood concentration difference.一种通过测量门静脉和体循环血液浓度差异来建立肝肠循环的再循环模型。
J Pharmacokinet Pharmacodyn. 2003 Apr;30(2):119-44. doi: 10.1023/a:1024415730100.
6
Introduction of recirculatory analysis into portal and systemic concentration difference method.
Biol Pharm Bull. 2001 Nov;24(11):1298-304. doi: 10.1248/bpb.24.1298.
7
Alternative continuous infusion method for analysis of enterohepatic circulation and biliary excretion of cefixime in the rat.用于分析大鼠体内头孢克肟肝肠循环和胆汁排泄的交替连续输注法
J Pharm Sci. 1994 Jun;83(6):819-23. doi: 10.1002/jps.2600830612.
8
[Disposition analysis by fast inverse Laplace transform (FILT)].[通过快速逆拉普拉斯变换(FILT)进行处置分析]
Yakugaku Zasshi. 1992 Aug;112(8):503-15. doi: 10.1248/yakushi1947.112.8_503.
9
Two-compartment dispersion model for analysis of organ perfusion system of drugs by fast inverse Laplace transform (FILT).用于通过快速拉普拉斯逆变换(FILT)分析药物器官灌注系统的双室弥散模型。
J Pharmacokinet Biopharm. 1989 Apr;17(2):179-202. doi: 10.1007/BF01059027.
10
Short-period double-dosing for simultaneous evaluation of intestinal absorption and hepatic disposition in a single conscious rat using cephalexin as test drug.以头孢氨苄为受试药物,在清醒大鼠个体中采用短周期双倍给药法同时评估肠道吸收和肝脏处置情况。
J Pharm Pharmacol. 1997 Dec;49(12):1189-94. doi: 10.1111/j.2042-7158.1997.tb06068.x.

引用本文的文献

1
A recirculatory model with enterohepatic circulation by measuring portal and systemic blood concentration difference.一种通过测量门静脉和体循环血液浓度差异来建立肝肠循环的再循环模型。
J Pharmacokinet Pharmacodyn. 2003 Apr;30(2):119-44. doi: 10.1023/a:1024415730100.
2
Evaluation of intestinal absorption into the portal system in enterohepatic circulation by measuring the difference in portal-venous blood concentrations of diclofenac.通过测量双氯芬酸门静脉血浓度差异评估肠肝循环中肠道对门静脉系统的吸收情况。
Pharm Res. 1995 Jun;12(6):880-3. doi: 10.1023/a:1016217221977.

本文引用的文献

1
Determination of renal clearance using arterial and venous plasma: procainamide in rabbits.
J Pharm Sci. 1981 Dec;70(12):1373-5. doi: 10.1002/jps.2600701223.
2
Arterial-venous plasma concentration differences of six drugs in the dog and rabbit after intravenous administration.
Res Commun Chem Pathol Pharmacol. 1981 Apr;32(1):27-39.
3
Arterial and venous blood sampling in pharmacokinetic studies: propranolol in rabbits and dogs.
Res Commun Chem Pathol Pharmacol. 1981 Jul;33(1):33-48.
4
Moments of physiological transit time distributions and the time course of drug disposition in the body.生理转运时间分布的时刻以及药物在体内处置的时间进程。
J Math Biol. 1982;15(3):305-18. doi: 10.1007/BF00275690.
5
Effect of arterial-venous plasma concentration differences on the determination of mean residence time of drugs in the body.
Res Commun Chem Pathol Pharmacol. 1982 Jan;35(1):17-26.
6
Hemodynamic influences upon the variance of disposition residence time distribution of drugs.血流动力学对药物处置停留时间分布方差的影响。
J Pharmacokinet Biopharm. 1983 Feb;11(1):63-75. doi: 10.1007/BF01061768.
7
Modelling of initial distribution of drugs following intravenous bolus injection.
Eur J Clin Pharmacol. 1983;24(1):121-6. doi: 10.1007/BF00613938.
8
Pharmacokinetics of methotrexate and 7-hydroxy-methotrexate in rabbits after intravenous administration.静脉注射后甲氨蝶呤和7-羟基甲氨蝶呤在兔体内的药代动力学
J Pharmacokinet Biopharm. 1983 Oct;11(5):499-513. doi: 10.1007/BF01062208.
9
Determination of metoprolol in human blood plasma using high-performance liquid chromatography.
J Chromatogr. 1983 Nov 11;278(1):204-8. doi: 10.1016/s0378-4347(00)84776-3.
10
Binding of beta-adrenoceptor antagonists to rat and rabbit lung: special reference to levobunolol.β-肾上腺素能受体拮抗剂与大鼠和兔肺的结合:特别提及左布诺洛尔。
Arzneimittelforschung. 1984;34(5):579-84.