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Dose-dependence of drug plasma level decline in dogs.

作者信息

Dayton P G, Cucinell S A, Weiss M, Perel J M

出版信息

J Pharmacol Exp Ther. 1967 Nov;158(2):305-16.

PMID:4169043
Abstract
摘要

相似文献

1
Dose-dependence of drug plasma level decline in dogs.犬类药物血浆水平下降的剂量依赖性。
J Pharmacol Exp Ther. 1967 Nov;158(2):305-16.
2
Physiological and physicochemical bases of drug interactions in man.人体中药物相互作用的生理和物理化学基础。
Ann N Y Acad Sci. 1971 Jul 6;179:67-87. doi: 10.1111/j.1749-6632.1971.tb46891.x.
3
An experimental model in dogs for studying interactions of drugs with bishydroxycoumarin.一种用于研究药物与双羟香豆素相互作用的犬类实验模型。
Clin Pharmacol Ther. 1969 Nov-Dec;10(6):817-25. doi: 10.1002/cpt1969106817.
4
Effects of phenobarbital or SKF 525A pretreatment on diphenylhydantoin disposition in pregnant mice.
Toxicol Appl Pharmacol. 1971 Dec;20(4):573-81. doi: 10.1016/0041-008x(71)90262-6.
5
Effect of phenylbutazone on the distribution, elimination and anticoagulant action of dicumarol in rats.保泰松对双香豆素在大鼠体内分布、消除及抗凝作用的影响。
J Pharmacol Exp Ther. 1973 Oct;187(1):176-84.
6
IV. Pharmacogenetics and drug toxicity. Variation of drug metabolism in animals and the prediction of drug action in man.
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7
Effect of phenobarbital on bishydroxycoumarin plasma concentrations and hypoprothrombinemic responses in sheep.苯巴比妥对绵羊双香豆素血浆浓度及低凝血酶原血症反应的影响。
Am J Vet Res. 1972 Apr;33(4):825-34.
8
Inhibition of drug metabolism by chloramphenicol.氯霉素对药物代谢的抑制作用。
Lancet. 1969 Dec 27;2(7635):1397-9. doi: 10.1016/s0140-6736(69)90937-4.
9
Drug interactions involving oral anticoagulants.
Cardiovasc Clin. 1974;6(2):23-41.
10
Pharmacokinetics of drugs in rabbits with experimental acute renal failure.
Pharmacology. 1978;17(6):307-14. doi: 10.1159/000136871.

引用本文的文献

1
Rate of elimination of tracer doses of phenytoin at different steady-state serum phenytoin concentrations in epileptic patients.不同稳态血清苯妥英浓度下癫痫患者示踪剂量苯妥英消除率。
Br J Clin Pharmacol. 1974 Apr;1(2):155-61. doi: 10.1111/j.1365-2125.1974.tb00225.x.
2
The Bateman function revisited: a critical reevaluation of the quantitative expressions to characterize concentrations in the one compartment body model as a function of time with first-order invasion and first-order elimination.重新审视贝特曼函数:对单室体内模型中作为时间函数的浓度进行定量表达的批判性重新评估,该模型具有一级侵入和一级消除过程。
J Pharmacokinet Biopharm. 1994 Apr;22(2):103-28. doi: 10.1007/BF02353538.
3
Quantitation of CSF concentrations and biological activity of probenecid metabolites.
丙磺舒代谢物脑脊液浓度及生物活性的定量分析。
Eur J Clin Pharmacol. 1980;17(3):223-6. doi: 10.1007/BF00561904.
4
The unsteady model. An alternative approach to nonlinear pharmacokinetics.非稳态模型。非线性药代动力学的另一种方法。
Eur J Clin Pharmacol. 1981;20(5):387-98. doi: 10.1007/BF00615410.
5
Clinical pharmacokinetics of probenecid.丙磺舒的临床药代动力学。
Clin Pharmacokinet. 1981 Mar-Apr;6(2):135-51. doi: 10.2165/00003088-198106020-00004.
6
Interspecies variation in liver weight, hepatic blood flow, and antipyrine intrinsic clearance: extrapolation of data to benzodiazepines and phenytoin.
J Pharmacokinet Biopharm. 1980 Apr;8(2):165-76. doi: 10.1007/BF01065191.
7
Genetic control of the phenobarbital-induced shortening of plasma antipyrine half-lives in man.苯巴比妥诱导人体血浆安替比林半衰期缩短的遗传控制。
J Clin Invest. 1969 Dec;48(12):2202-9. doi: 10.1172/JCI106186.
8
Pharmacokinetics of single and multiple doses of phenytoin in man.苯妥英钠单剂量及多剂量在人体中的药代动力学。
Eur J Clin Pharmacol. 1974;7(2):81-6. doi: 10.1007/BF00561319.
9
Kinetics of diphenylhydantoin elimination in rats.
J Pharmacokinet Biopharm. 1973 Apr;1(2):99-102. doi: 10.1007/BF01059624.
10
A modern view of pharmacokinetics.药物动力学的现代观点。
J Pharmacokinet Biopharm. 1973 Oct;1(5):363-401. doi: 10.1007/BF01059664.