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in vivo intestine absorption 在体肠吸收
Intestinal absorption dynamics provided a method for profound study on the process in vivo and new oral druges development. 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。
Adl2 ElB 55kDa binds hDaxx in vivo or in vitro. 共免疫沉淀反应和Western blot结果证实Ad12 E1B 55KD能在细胞内外与hDaxx直接结合。
Keywords Hup-A;Intestinal Absorption in situ;Hydrophilic Matrix Sustained Release Tablet;HPLC;Orthogonal design;Bioequivalence;in vivo and in vitro correlativity; 石杉碱甲;在体小肠吸收;亲水凝胶缓释骨架片;高效液相色谱法;正交设计;生物利用度;体内外相关性;
The expression product shows activity of antitumor in vivo. 表达产物在体内具有一定的抗肿瘤活性。
Result Nicardipine can induce rat mesangial cell apoptosis in vivo. 结论尼卡地平在体内有诱导大鼠系膜细胞凋亡的作用。
Methods Using the in vivo micropuncture technique in SD r ats. 方法利用活体微穿刺技术。
CONCLUSION Survivin T34A might inhibit A549 tumors growing in vivo. 结论 Survivin T34A在体内可明显抑制A549肺癌生长。
At last, tumorigenesis assay was undertaken in nude mice in vivo. 进行黑素瘤细胞体外克隆形成实验观察,计算各组细胞的克隆形成率;
The embryos from the in vivo fertilization develop best. 体内受精胚胎的体外发育最佳。
And, these monkeys were injected in vivo dose must SIV virus. 然后，这些猴子体内均被注入一定剂量的SIV病毒。
Conclusion The VH containing extra-sequence may exist in vivo. 结论提示这段异常序列在体内可能存在于该VH之中。
AIM: To study the correlation between the release rate in vitro and the absorption in vivo of Shenshen sustained-release Capsule(SSRC phenylethanoid glycosides). 目的:考察肾参缓释胶囊(苯乙醇苷)的体外释放度与体内吸收的相关性。
CONCLUSION:A good correlativity was showed between in vivo absorption and in vitro release of theophylline sustained release tablets. 结论：茶碱缓释片的体内吸收百分率与体外释放百分率间存在良好的相关关系。
METHODS: Using invivo rat intestinal absorption model and HPLC, the apparent small intestine absorption rate of protocatechualdehyde was mea-sured. 方法:利用大鼠在体肠吸收模型,以高效液相色谱法测定原儿茶醛的表观小肠吸收速率。
OBJECTIVE：To evaluate the correlativity between in vitro release and in vivo absorption of theophylline sustained release tablets. 目的：评价茶碱缓释片的体外释放与体内吸收的相关性，为其质量控制提供实验依据。
With the increasing exploitation of new medicaments, absorption, distribution, metabolism, excretion and toxicity (ADME/T) of drugs in vivo have been attached importance to. 随着新药的不断开发,药物在生物体内的吸收、分布、代谢、排泄和毒性(ADME/T)等性质已经引起了人们的高度重视。
Conclusions There is a significant correlation between the absorption in vivo and the dissolution in vitro of a compound extended-release dipyridamole/aspirin capsules. 结论阿司匹林双嘧达莫缓释胶囊体外释放质量百分率和体内吸收质量百分率呈显著相关。
The sufficient absorption of drug in gastrointestinal tract is a prerequisite for its activity in vivo by oral,and determines the distribution,metabolism and excretion of itself. 药物于胃肠道的吸收是口服给药产生体内活性的先决条件,决定着药物的分布、代谢和排泄。
Method: The gastric emptying of rat, small intestinal vermiculation and the movement of vivo intestinal smooth muscle of rabbit were observed. 方法：分别采用小鼠胃排空和小肠推进及兔在体肠蠕动实验，研究莱菔子不同炮制品对消化系统的药理作用。