The factors on drug release were investigated.
体外考察影响药物释放的因素。
Conclusion the drug release mainly depends on the gel erosion.
结论药物释放主要取决于凝胶溶蚀。
Drug release was influenced by the method and the release medium.
药物释放受释放方法和递质的影响。
CONCLUSIONS the rate of drug release is proportional to the ionic strength.
结论：释药速率与离子强度之间存在较好的线性负相关关系。
The drug release and permeation were observed to be dependent on some factors.
药物的体外释放和渗透受到多种处方因素的调节。
The path led him to be a pioneer of controlled drug release and tissue regeneration.
这条路引领着他成为药物控制释放和组织工程的先锋人物。
The materials are suitable for making soft contact lens and drug release matrix.
用本法合成的材料是制作较接触镜及药物慢释放基质的理想材料。
Results: Drug release rate of the tablets did not change with the change of medium.
结果：渗透泵的释药不随释药环境的改变而改变。
Taking Ib as a model drug, the drug release behaviors of the capsules were studied.
以布洛芬为模型药物，初步研究了微囊载体的缓释行为。
OBJECTIVE To predict drug release from the extended formulations by grey maths model.
目的运用灰色数学理论预测长效缓释蛋白微球的体外释药过程。
OBJECTIVE: To prepare sustained release tablets and evaluate its drug release property.
目的：制备美沙拉嗪缓释片剂，并评价其体外释放特性。
OBJECTIVE To prepare thymopentin microspheres and investigate the drug release in vitro.
目的制备胸腺五肽微球并对其体外释放进行考察。
This paper summarizes the progress of research on liposomes for controlled drug release.
综述了药物控释用脂质体的研究进展情况。
This study focuses on mathematical modeling of drug release from PLGA cylindrical millirods.
这项研究集中在药物从PLGA圆筒型微囊中释放的数学模型。
This so-called intelligent drug release is also used to treat heart disease and other diseases.
这种所谓的智能药物释放系统还可用于心脏及其他疾病的治疗。
Methods the influencing factors on the drug release were investigated by use of similarity factor method.
方法采用相似因子法考察影响药物释放速率的因素，并考察了其释药机理。
Objective To prepare aciclovir sustained-release pellets and investigate the drug release mechanism in vitro.
目的制备阿昔洛韦缓释微丸，并对其体外释药情况进行研究。
Results the gel erosion and drug release were increased with the increase of surface area and shaking frequency.
结果凝胶溶蚀和药物释放随着振荡频率和释放面积的增加而加快。
The results showed that the drug release from MTX liposomes was in conformity with the first-order dynamic equation.
结果表明：甲氨喋呤脂质体的药物释放速率符合一级动力学方程。
Objective To study the preparation technique and in vitro drug release of adriamycin gelatin microspheres (ADM-GMS).
目的对阿霉素明胶微球（ADM-GMS）的制备工艺及体外释药特性进行研究。
Methods Coating prescription was optimized by uniform design and the drug release characteristic was tested in vitro.
方法采用均匀设计优化包衣处方，对度米芬渗透泵片进行体外释放度试验。
OBJECTIVE To prepare sustained-release Hippophae rhamnoides(TFH) tablet and evaluate the rule of drug release property.
目的评价醋柳黄酮缓释片的缓释效果并考察其体外释放规律。
OBJECTIVE To study the preparation process, assay and in vitro drug release of adriamycin polylactic acid microspheres.
目的：对阿霉素聚乳酸微球的制备工艺、含量测定及体外释药特性进行初步研究。
The results showed that the lag time before drug release was lengthened with the increase of the viscosity grade of HPMC.
结果表明，HPMC粘度增加使药物释放滞后时间延长，但高粘度HPMC会导致药物释放无明显突跃点；
Aim to prepare the micelles of stearic acid grafted chitosan oligosaccharide and investigate the drug release from micelles.
目的考察阳离子型壳寡糖硬脂酸嫁接物胶团的理化性质及载药胶团的体外药物释放。
The injectable hydrogel for its unique phase transition behavior is expected to be widely used in the field of drug release.
其中，可注射水凝胶因其独特的溶胶-凝胶相转变性质，在药物控制释放领域有着广泛应用。
Aim To prepare ondansetron hydrochloride osmotic pump tablets (OND-OPT) and investigate their in vitro drug release behavior.
目的制备盐酸昂丹司琼渗透泵型控释片剂(OND - OPT)并考察体外释药特性。
OBJECTIVE To evaluate drug release properties in vitro of the hydrogel films made of cross-linked hyaluronic acid derivatives.
目的对交联透明质酸衍生物制备的载药水凝胶膜进行体外药物释放研究。
The formalation design for oral DDS or GIDS is essential to achieveprolonging stomach residence time and improving drug release.
经口给药的DDS大多以延长药剂在胃内滞留时间和改善药物释放为其设计出发声点。
CONCLUSION The TFH tablet has sustained release property in vitro. The drug release pattern is in accord with Weibull distribution.
结论醋柳黄酮缓释片缓释效果显著，体外释放符合威布尔分布模型。
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