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药物置换相互作用的动力学

Kinetics of drug displacement interactions.

作者信息

Aarons L J, Rowland M

出版信息

J Pharmacokinet Biopharm. 1981 Apr;9(2):181-90. doi: 10.1007/BF01068081.

DOI:10.1007/BF01068081
PMID:7277208
Abstract

A simple model simulating the kinetics of drugs displacement kinetics is investigated. It is demonstrated that for highly bound, lowly cleared drugs, displacement interactions are transitory. Consequently, the kinetics of the interaction have to be considered as well as the in vitro interaction. It is possible to have a significant in vitro displacement interaction with no in vivo counterpart. Methods of moderating drug displacement by adjusting the rate and the timing of administration of the displacing agent are discussed.

摘要

研究了一个模拟药物置换动力学的简单模型。结果表明,对于高结合率、低清除率的药物,置换相互作用是短暂的。因此,必须考虑相互作用的动力学以及体外相互作用。有可能在体外有显著的置换相互作用,但在体内却没有相应的情况。讨论了通过调整置换剂给药速率和时间来调节药物置换的方法。

相似文献

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Kinetics of drug displacement interactions.药物置换相互作用的动力学
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2
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SULPHAPHENAZOLE-INDUCED HYPOGLYCAEMIC ATTACKS IN TOLBUTAMIDE-TREATED DIABETICS.磺胺苯吡唑诱发甲苯磺丁脲治疗的糖尿病患者低血糖发作
Lancet. 1963 Dec 21;2(7321):1298-301. doi: 10.1016/s0140-6736(63)90847-x.
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The effect of various drugs on the binding of warfarin-14C to human albumin.各种药物对华法林 -14C 与人白蛋白结合的影响。
Biochem Pharmacol. 1967 Jul 7;16(7):1219-26. doi: 10.1016/0006-2952(67)90153-0.
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Potentiation of anticoagulant effect of warfarin by phenylbutazone.保泰松对华法林抗凝作用的增强作用。
人源肝细胞和细胞色素 P450 选择性抑制剂比人源重组 P450 更能准确预测人体药物暴露的个体差异。
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Quantitative Prediction of Drug-Drug Interactions Involving Inhibitory Metabolites in Drug Development: How Can Physiologically Based Pharmacokinetic Modeling Help?药物研发中涉及抑制性代谢物的药物相互作用的定量预测:基于生理的药代动力学建模如何提供帮助?
CPT Pharmacometrics Syst Pharmacol. 2016 Oct;5(10):505-515. doi: 10.1002/psp4.12110. Epub 2016 Sep 19.
5
Pharmacological inhibition of ALDH1A in mice decreases all-trans retinoic acid concentrations in a tissue specific manner.对小鼠体内乙醛脱氢酶1A(ALDH1A)进行药理抑制会以组织特异性方式降低全反式维甲酸的浓度。
Biochem Pharmacol. 2015 Jun 1;95(3):177-92. doi: 10.1016/j.bcp.2015.03.001. Epub 2015 Mar 9.
6
Importance of multi-p450 inhibition in drug-drug interactions: evaluation of incidence, inhibition magnitude, and prediction from in vitro data.多细胞色素 P450 抑制在药物相互作用中的重要性:从体外数据评估发生率、抑制程度和预测。
Chem Res Toxicol. 2012 Nov 19;25(11):2285-300. doi: 10.1021/tx300192g. Epub 2012 Sep 27.
7
Serum protein binding of nonsteroidal antiinflammatory drugs: a comparative study.非甾体抗炎药的血清蛋白结合:一项比较研究。
J Pharmacokinet Biopharm. 1997 Feb;25(1):63-77. doi: 10.1023/a:1025719827072.
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Ceftriaxone--bilirubin-albumin interactions in the neonate: an in vivo study.头孢曲松在新生儿体内与胆红素 - 白蛋白的相互作用:一项体内研究。
Eur J Pediatr. 1993 Jun;152(6):530-4. doi: 10.1007/BF01955067.
9
Plasma protein binding displacement interactions--why are they still regarded as clinically important?血浆蛋白结合置换相互作用——为何它们仍被视为具有临床重要性?
Br J Clin Pharmacol. 1994 Feb;37(2):125-8. doi: 10.1111/j.1365-2125.1994.tb04251.x.
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What is the true clinical significance of plasma protein binding displacement interactions?
Drug Saf. 1995 Apr;12(4):227-33. doi: 10.2165/00002018-199512040-00001.
N Engl J Med. 1967 Mar 2;276(9):496-501. doi: 10.1056/NEJM196703022760904.
4
Drug displacement from protein binding: isolation of a redistributional drug interaction in vivo.药物从蛋白结合位点的置换:体内一种再分布性药物相互作用的分离
Br J Pharmacol. 1971 Oct;43(2):312-24.
5
Impact of aspirin and chlorthalidone on the pharmacodynamics of oral anticoagulant drugs in man.阿司匹林和氯噻酮对人体口服抗凝药物药效学的影响。
Ann N Y Acad Sci. 1971 Jul 6;179:173-86. doi: 10.1111/j.1749-6632.1971.tb46898.x.
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Warfarin-phenylbutazone interaction in man: a long term multiple dose study.华法林与保泰松在人体中的相互作用:一项长期多剂量研究。
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Biochem Pharmacol. 1978 Jan 1;27(1):139-44. doi: 10.1016/0006-2952(78)90275-7.