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1)  drug absorption pharmacokinetics
药物吸收动力学
2)  Uptake kinetics
吸收动力学
1.
NH_4~+ and NO_3~- uptake kinetics of three aquatic macrophytes;
三种水生植物对不同形态氮素吸收动力学研究
2.
Studies on Uptake kinetics of Soluble Reactive Phosphorus(SRP) by Microplankton in Xiamen Harbor;
厦门港浮游生物对可溶性活性磷(SRP)吸收动力学的研究
3.
The characteristics of K+ uptake kinetics of four flue-cured tobacco genotypes were studied and their whole cell transmembrane inward K+ current of root cortex protoplast were recorded.
对4个烤烟基因型进行了根系钾吸收动力学特性研究,并对其根皮层细胞质膜内向跨膜钾电流进行了全细胞记录。
3)  pharmacokinetics [英][,fɑ:məkəu,kai'netiks]  [美][,fɑrməkokɪ'nɛtɪks, -kaɪ-]
吸收动力学
1.
Gender difference of nimodipine pharmacokinetics in rats;
大鼠口服尼莫地平吸收动力学性别差异研究
4)  Absorption kinetics
吸收动力学
1.
Studies on absorption kinetics of paeonol and paeonol-β-CD in rat s intestines;
丹皮酚与丹皮酚-β环糊精包合物大鼠在体小肠吸收动力学对照
2.
Absorption kinetics of Cepharanthine in the intestines of rats;
千金藤素在大鼠肠道内的吸收动力学
3.
Study on the absorption kinetics of simvastatin in rat small intestine;
辛伐他汀大鼠在体小肠吸收动力学
5)  Drug absorption
药物吸收
1.
Study on in vitro models of drug absorption;
药物吸收体外研究方法的概述
2.
Caco-2 cell model——an effective tool for the research of drug absorption;
Caco-2细胞模型——药物吸收研究的有效“工具”
3.
Methods Based on 32 papers published from 1974 to 2004,the different routes of drug transport in Caco2 cell monolayers are compared with those seen in vivo and the prediction of drug absorption in vivo from transport experiments in cell monolayers is discussed for different classes of drug.
方法在引用了自1974~2004年的32篇文献的基础上,通过介绍并比较体外Caco 2模型和体内药物吸收转运的不同途径,讨论Caco 2单层细胞模型在预测不同类药物体内吸收中的作用。
6)  pharmacokinetics [英][,fɑ:məkəu,kai'netiks]  [美][,fɑrməkokɪ'nɛtɪks, -kaɪ-]
药物动力学
1.
Determination of Ambroxol in Human Plasma by HPLC and Its Pharmacokinetics Study;
高效液相色谱法测定人血浆中氨溴素及药物动力学研究
2.
Determination of flunarizine in plasma by HPLC and its pharmacokinetics study;
高效液相色谱法测定盐酸氟桂利嗪血浆浓度及其药物动力学
3.
Studies on Paracetamol Liquid and Its Pharmacokinetics in Healthy Volunteers;
对乙酰氨基酚溶液剂及其药物动力学研究
补充资料:药物吸收动力学
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性质:口服或肌注给药后,药物在到达系统循环之前要涉及许多过程,包括药物制剂的分解,活性成分的溶出,药物向吸收部位转运和药物真正被吸收,药物一旦进入系统循环后就分布到各组织中并经肾脏和肝脏消除,这些过程同时发生。药物的吸收通常服从一级动力学,即吸收速率与吸收部位的药量成正比。

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