体内过程

药物转运体与药物体内过程

Drug transporter and the disposition of drug in the body

~（125）碘-眼镜蛇心脏毒素在大、小白鼠体内过程

Disposition of ~ ( 125 ) 1 - cardiotoxin from cobra venom in mice and rats

阿司匹林维生素C泡腾片的体内过程及生物等效性

Relative bioavailability of effervescent tablet of aspirin-vitamin C in healthy volunteers

min。结论：灯盏细辛注射液中的总咖啡酯类成分在大鼠体内过程符合静脉注射二室模型。

Conclusion : The pharmacokinetics model of coffeic acid esters is two-compartment model after iv Erigeron injection in Sprague-Dawley rats .

目的：改进动物急性累计死亡率法（ACD法），使其适于测算口服中药体内过程。

AIM : To improve the acute cumulative death rates method ( ACD method ) in animal by oral administration .

方法：采用HPLC-MS分析对大鼠口服麦冬皂苷肠溶微球的代谢产物之一薯蓣皂苷元进行体内过程的监测。

METHODS : HPLC-MS method of determining rat 's metabolite diosgenin in vivo was established after single-dose oral Ophiopogon japonicus saponin enteric microsphere .

10名志愿者随机交叉口服单剂量100mg二种国产尼莫地平片剂后，以本法测定其体内过程符合一室模型。

The pharmacokinetics of nimodipine was determined by this GC ECD method following a single oral dose of 100 mg of two kinds of domestic nimodipine tablets given to each of 10 volunteers in an open randomized two way crossover design .

对10名健康志愿者口服azithromycin的药物动力学研究以及其干糖粉的相对生物利用度测定结果显示：空腹口服azithromycin单剂500mg后，其体内过程符合二室模型，其消除半衰期为50.39±8.87h；

The pharmacokinetics of azithromycin and the bioavailability of its dry syrup in 10 healthy volunteers were described in this paper . After a single oral dose of 500 mg azithromycin administration in fasting state , the serum concentration time curves appeared to fit a two compartment model kinetics .

固体口服制剂体内过程影响因素的分析研究

The Effects of in Vivo Process for Solid Oral Dosage Forms

以唾液样本验证对乙酰氨基酚延迟释放片体内过程

The Formulation Proof of Acetaminophen Delayed - Release Tablets in Vivo

五价葡萄糖酸锑钙在狗体内过程的初步研究

The Sojourn of Calcium Antimony ( Pentavalent ) Gluconate in Dogs

结论：受试者单剂空腹口服国产妥舒沙星片剂后体内过程和进口品相仿。

CONCLUSION : The pharmacokinetics of domestic and imported tosulfloxacin is similar .

结合文献研究表明灯盏花素的体内过程相对复杂。

Relative documents and reserches illustrated complicated process in vivo of Breviscapine .

人血清白蛋白修饰的尿激酶与天然尿激酶的家兔体内过程比较

Disposition of human serum albumin modified urokinase in rabbits

结果经3P97程序拟合处理，两者的体内过程符合一室模型。

Results Both the two domestic ciprofloxacin tablets fit to one compartment model .

氟脲嘧啶三种给药途径的体内过程研究

The investigation of disposition of 5-fluorouracil in vivo after three routes of administrations

由一个地方或阶段到另一个地方或阶段的一种体内过程。

A bodily process of passing from one place or stage to another .

重组人内抑素药物代谢动力学及体内过程研究

The Study of Pharmacokinetics of Recombine Human Endostatin and Its Process Within Body

H-咖啡酸的体内过程研究

The Fate of ~ 3H-Caffeic Acid in Vivo

乌拉地尔缓释胶囊的含量测定及其体内过程研究

Determination of Sustained - release Urapidil Capsule and Study of Its in Vivo Process

蜂毒口服包衣微丸体内过程的初步评价五个部分。

The evaluation of the OCDS in vivo .

复方甘氨酸茶碱钠的体内过程及相对生物利用度研究

Study on bioavailability of theophylline and guaifenesin from theophylline sodium glycinate-guaifenesin preparations in healthy volunteers

目的：研究泻心汤配伍沉淀物的大鼠体内过程。

Objective : To study the process in vivo of the components in the precipitation of Xiexin decoction .

结论本实验建立的无细胞凋亡体系可以高效的诱导外源细胞核凋亡，重现体内过程。

Conclusion The prepared cell-free apoptotic system can effectively induce isolated nuclei apoptosis and mimick the process in vivo .

目的：考察胸腺肽α1（Tα1）结肠释放片的体内过程。

Objective : To investigate the in vivo behavior of colon-targeted thymosin α 1 ( T α 1 ) tablets .

基于体内过程的中药有效成分和有效效应物质的发现策略

Discovery strategy for effective and active constituents of Chinese material medica based on processes of metabolism and disposition in intra-body

肠吸收动力学研究为深入研究其体内过程及新的口服给药系统提供了研究思路。

Intestinal absorption dynamics provided a method for profound study on the process in vivo and new oral druges development .

综述了聚合物胶束的自组装原理和结构、制备方法、体内过程和应用等。

The self-assemble principle and structure of polymeric micelles are reviewed as well as their preparation , in vivo process and applications .

目的建立加替沙星的反相高效液相色谱分析方法，并对其肝损害模型动物体内过程与药代动力学进行分析研究。

Objective To establish HPLC method for determination of gatifloxacin and to , analyze in vivo course and pharmacokinetics in animals model of liver damaged .

20名健康受试者随机交叉口服克拉霉素干混悬剂和片剂后，其体内过程符合一室模型，统计学结果表明两种制剂生物等效。

The results of pharmaco-kinetics study after oral administration clarithromycin preparations showed that the two formulations conformed to one compartment model and they were bio-equivalent .