大家在查： Chewco 萧万长海惟一 2008年4月8日 antimalarials 0—15千 5.377 露露面离子型 Manji

释药

网络release; drug release

释药

释药

release

药学百科--生物医药百科词典 ... preparations - 制剂 release - 释药 tablets - 片剂 ...

drug release

零级释药,zero-order sustained... ... ) zero-order release 零级释放 ) drug release 释药 ) Drug-release 释药 ...

1

2

When increasing the quantities of citric acid , there was a trend favoring the mechanism of diffusion and the dissolution rates increased .

随着枸橼酸用量的不断增加，药物释放机制更靠近扩散过程，且释药速度逐渐增加。

3

CONCLUSION Accelerated release testing could be applied to evaluate the drug release profile of huperzine A PLGA microspheres .

结论：加速释放度试验可用于快速评价石杉碱甲微球的释药特性。

4

RESULTS The release and swelling behavior of the alginate beads showed significant difference after being crosslinked with different ions .

结果不同离子交联制备的海藻酸凝胶微丸的溶胀行为和释药行为有明显差异。

5

7

8

Experimental results showed that the release speed of composite microspheres was faster than that of sodium alginate gel microspheres .

实验结果表明，复合微球释药速率比海藻酸钠凝胶微球慢。

10

Objective : To prepare gastric floating sustained-release tablets of sodium ferulate and evaluate its release characteristics in vitro .

目的：制备阿魏酸钠胃漂浮片，评价其体外释药性能。

12

The effect of the osmotic pressure difference across the membrane on release rate was studied.

药物在相同渗透压的不同溶出介质中具有相同的释药速率；

14

Objective : To prepare the dextromethorphan oral sustained-release suspensions and study the in-vitro release kinetics.

目的：制备右美沙芬树脂口服缓释混悬液，并考察其释药特性。

15

Invitro release of naltrexone microspheres prepared with the various PLGA were compared .

以其为载体制备纳曲酮微球，比较了体外释药速率。

16

Adriamycin PLGA microspheres can reach sustained-releasing requirement for treating tumors .

阿霉素 PLGA 微球能达到治疗肿瘤的长效释药的要求。

19

The pulsatile-release mechanism of the tablets was proved by the water take-up experiments .

通过吸水实验分析脉冲片的释药机制。

23

OBJECTIVE The effect of different diluents on the release rate of insoluble drug from HPMC hydrogel matrix was investigated.

目的探讨稀释剂对难溶性药物的 HPMC 骨架片释药的影响。

27

The absorbency of the drug in PBS was detected and the velocity of drug release was counted by UV -visible spectroscopy .

通过紫外分光光度计检测其释放在磷酸缓冲溶液（PBS ）中药物的吸光度，并计算其释药速率。

29

30

Objective : To prepare curcumin albumin nanosuspensions and study its release characteristics in vitro .

目的：制备姜黄素白蛋白纳米混悬剂，并考察其体外释药性能。

热词推荐

大家在看