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Derivation of general equations for linear mammillary models when the drug is administered by different routes.

作者信息

Vaughan D P, Trainor A

出版信息

J Pharmacokinet Biopharm. 1975 Jun;3(3):203-18. doi: 10.1007/BF01067909.

DOI:10.1007/BF01067909
PMID:1159624
Abstract
摘要

相似文献

1
Derivation of general equations for linear mammillary models when the drug is administered by different routes.
J Pharmacokinet Biopharm. 1975 Jun;3(3):203-18. doi: 10.1007/BF01067909.
2
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.
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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.
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Model independent derivation of general equations for the "first-pass" effect and extra-hepatic drug elimination.“首过”效应和肝外药物消除通用方程的模型无关推导。
Eur J Clin Pharmacol. 1977;11(1):57-64. doi: 10.1007/BF00561789.
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[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.
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Linear pharmacokinetic equations allowing direct calculation of many needed pharmacokinetic parameters from the coefficients and exponents of polyexponential equations which have been fitted to the data.线性药代动力学方程允许根据已拟合数据的多指数方程的系数和指数直接计算许多所需的药代动力学参数。
J Pharmacokinet Biopharm. 1976 Oct;4(5):443-67. doi: 10.1007/BF01062831.
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Number of exponential terms describing the solution of an N-compartmental mammillary model: vanishing exponentials.描述 N 房室乳头状模型解的指数项数量：消失的指数项。
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[Sampling design of linear one compartment open model for drug administered via non-blood-vessel way (author's transl)].
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General theory for rapidly establishing steady state drug concentrations using two consecutive constant rate intravenous infusions.
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[Model building in pharmacokinetics/Part IV: Derivation of microconstants in linear compartment models (author's transl)].
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引用本文的文献

1
Understanding the dose-effect relationship: clinical application of pharmacokinetic-pharmacodynamic models.理解剂量-效应关系：药代动力学-药效学模型的临床应用
Clin Pharmacokinet. 1981 Nov-Dec;6(6):429-53. doi: 10.2165/00003088-198106060-00002.
2
Linear pharmacokinetic models and vanishing exponential terms: implications in pharmacokinetics.线性药代动力学模型与消失指数项：对药代动力学的影响
J Pharmacokinet Biopharm. 1976 Oct;4(5):395-425. doi: 10.1007/BF01062829.
3
Model independent derivation of general equations for the "first-pass" effect and extra-hepatic drug elimination.

本文引用的文献

1
Multicompartment pharmacokinetic models and pharmacologic effects.多房室药代动力学模型与药理效应。
J Pharm Sci. 1969 Apr;58(4):422-4. doi: 10.1002/jps.2600580406.
2
Digoxin metabolism in the elderly.老年人地高辛的代谢
Circulation. 1969 Apr;39(4):449-53. doi: 10.1161/01.cir.39.4.449.
3
Some pharmacokinetic aspects of 5-(dimethylriazeno)-imidazole-4-carboxamide in the dog.5-（二甲基三氮烯基）-咪唑-4-甲酰胺在犬体内的一些药代动力学方面
“首过”效应和肝外药物消除通用方程的模型无关推导。
Eur J Clin Pharmacol. 1977;11(1):57-64. doi: 10.1007/BF00561789.
4
Number of exponential terms describing the solution of an N-compartmental mammillary model: vanishing exponentials.描述 N 房室乳头状模型解的指数项数量：消失的指数项。
J Pharmacokinet Biopharm. 1979 Oct;7(5):511-25. doi: 10.1007/BF01062392.
J Pharm Sci. 1968 Dec;57(12):2126-31. doi: 10.1002/jps.2600571221.
4
Pharmacokinetic basis for the influence of route of administration on the area under the plasma concentration-time curve.给药途径对血浆浓度-时间曲线下面积影响的药代动力学基础。
J Pharm Sci. 1969 Dec;58(12):1477-80. doi: 10.1002/jps.2600581211.
5
Use of general partial fraction theorem for obtaining inverse laplace transforms in pharmacokinetic analysis.在药代动力学分析中使用一般部分分式定理来获取拉普拉斯逆变换。
J Pharm Sci. 1971 Oct;60(10):1593-4. doi: 10.1002/jps.2600601041.
6
General treatment of linear mammillary models with elimination from any compartment as used in pharmacokinetics.线性乳突模型的一般处理方法，即如药代动力学中所使用的那样，从任何隔室中消除。
J Pharm Sci. 1972 Apr;61(4):536-41. doi: 10.1002/jps.2600610408.
7
Pharmacokinetics of trichloroethanol and metabolites and interconversions among variously referenced pharmacokinetic parameters.三氯乙醇及其代谢产物的药代动力学以及各种引用的药代动力学参数之间的相互转化。
J Pharm Sci. 1973 Apr;62(4):550-72. doi: 10.1002/jps.2600620404.
8
Pharmacokinetics of absorption, distribution and elimination of fenfluramine and its main metabolite in man.
J Pharm Pharmacol. 1972 Feb;24(2):108-14. doi: 10.1111/j.2042-7158.1972.tb08942.x.
9
Pharmacokinetics of pentazocine in the rhesus monkey.
J Pharm Sci. 1974 Jan;63(1):84-8. doi: 10.1002/jps.2600630121.
10
Comparative pharmacokinetics of coumarin anticoagulants. IV. Application of a three-compartmental model to the analysis of the dose-dependent kinetics of bishydroxycoumarin elimination.香豆素类抗凝剂的比较药代动力学。IV. 三室模型在双香豆素消除剂量依赖性动力学分析中的应用。
J Pharm Sci. 1968 Nov;57(11):1888-95. doi: 10.1002/jps.2600571113.