solid dispersion

The pharmacokinetic study showed that the both serum iron concentration in rats rose obviously after the administration of enteric-coated APIC solid dispersion and Niferex and the AUC of both drugs increased accordingly as the accrescence of the dosage in the dosage range chose in this experiment.

药动实验结果显示APIC肠溶固体分散体与力蜚能给药后大鼠体内血铁浓度均有显著升高，且两种药物在本实验所选剂量范围内AUC都随给药剂量增大而增加。

TESTING Experimental Study on Explosive Dispersion of Solid-Liquid Fuels For FAE Devices with a Special Charge Structure

固液装药结构的FAE爆炸抛撒试验研究

Considering the reflection inside the solid immersion lens, and using vector diffraction theory, the influences of dispersion to the transmitted field characters of hemisphere SIL ( h-SIL) are analyzed.

在考虑了半球型固体浸没透镜（h-SIL）内部的反射，应用矢量衍射理论分析了色散对h-SIL的透射场特性的影响。

OBJECTIVE To prepare etoposide solid dispersion to enhance the dissolution rate.

目的制备依托泊苷固体分散体,改善依托泊苷的溶出度.

Study on the solid dispersion of ACV preparation

无环鸟苷固体分散体的研究

Conclusion: Solid dispersion improved the stability and dissolution of compound hawthorn dropping pills.

结论: 复方山楂滴丸固体分散体提高了药物稳定性和溶解性.

Objective: To enhance the dissolution rate of Curcumin ( Cur) by solid dispersion technique.

目的：利用固体分散技术提高难溶性药物姜黄素的体外溶出速率。

Objective To investigate the stability of Nitrendipine solid dispersion pellets.

目的考察尼群地平固体分散体微丸的稳定性.

Objective To optimize the method of preparing Dragon's blood solid dispersion.

目的确定制备龙血竭固体分散体的最佳方法.

CONCLUSION Itraconazole solid dispersion can significantly increase it's solubility and dissolution rate.

结论：伊曲康唑固体分散体能明显提高伊曲康唑的溶解度及体外溶出速率。

Conclusion Solid dispersion is able to release rapidly as an ameliorated technic.

结论固体分散体有速释作用,可考虑用固体分散技术改进降酶灵胶囊的制备工艺.

So we prepared enteric-coated APIC solid dispersion and investigated its properties in vivo and in vitro and the feasibility of APIC absorbed mainly in the form of polysaccharide-iron molecule in enteric-coated preparation.

因此本文将APIC制备成肠溶固体分散体，并对其体内外性能和肠溶性制剂中APIC绝大部分以多糖铁分子形式吸收的可行性进行考察。

Method: The solid dispersion method was used , dissolution was determined in vitro.

方法: 采用固体分散体制备头孢克肟口含片, 测定其体外溶出度进行评价.

OBJECTIVE To study the formation and solubilization mechanism of cefuroxime axetil solid dispersion.

目的探讨头孢呋辛酯聚维酮固态分散体形成和改善溶出的机制.

Solid lipid nanoparticles aqueous dispersion loaded ethyl acetate extract of Tripterygium wilfordii Hook.

制备雷公藤乙酸乙酯提取物固体脂质纳米粒水分散体,并初步研究了体外透皮行为.

CONCLUSION: The types of carriers and drug-carrier ratio had great effect on the characteristics of in vitro dissolution and enthalpy change of lornoxicam solid dispersion.

结论：载体类型及药物载体比例影响氯诺昔康固体分散体的体外溶出特性及热焓变化。

Dissolution rate of Aciclovir solid dispersion and its relative bioavailability in human

固体分散无环鸟苷胶囊剂溶出度及人体内生物利用度

Studies on formation and solubilizing mechanism of oleanolic acid solid dispersion

齐墩果酸固体分散体形成和增溶机制研究

Objective To enhance the dissolution rate of ketoprofen ( KPF ) by adopting the solid dispersion method.

目的提高难溶性药物酮洛芬体外溶出速度.