The results show that the water uptake ability, the water maintenance ability, drug release efficiency and degradable behavior are related to the proportion of components in the sponge.
海绵的吸水率和保水率、药物缓释性能以及酶降解性能随聚乙烯醇与壳聚糖、明胶混合比例的改变而改变。
The effect of the size, surface area and porosity of particles, the property and content of drugs, as well as the properties of polymer on the drug release behavior of microcapsules are elucidated.
阐述了高分子包囊的粒径、表面积、孔度、药物性能和药含量，以及高分子包囊材料的性能对药物释放行为的影响。
At the same time, the influences of the drug-fed amount on PMT and release behavior in vitro of PMT were investigated.
同时，还研究了投药量对PMT的影响及PMT的体外药物释放行为。
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 Clarithromycin floating beads and investigate its buoyancy, entrapment efficiency and drug release behavior in vitro.
目的制备克拉霉素胃漂浮小丸，考察其漂浮性，包封率和体外释药行为。
The factors which affect the lag time and drug release behavior were investigated, such as the type and thickness of the inner and outer layers, the type and amount of the plasticizer, etc.
本文考察了溶胀层种类和厚度、控释层包衣液类型和包衣层厚度、增塑剂种类和用量等因素对时滞及药物释放速率的影响。
The vitro release result which used theophylline as model drug showed, the release behavior can divide to sharp release , relaxedly release and equilibrium release periods.
以茶碱为模型药物，模拟体外释放的结果表明，共聚物胶束对茶碱的体外释药可分为突释、缓慢释放、平衡释放三个阶段。
The release behavior of the drug from liposome was studied by the third method for dissolution.
用溶出度第三法考察了脂质体的释放规律。
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。
CONCLUSION the adhesive property of the tablets and the release behavior of drug are relevant. Also, the formulation of buccal adhesive tablets is optimized by adjusting the composition.
结论口颊黏附片的生物黏附性与体外释药行为具有一定的相关性，通过调整处方可筛选出生物黏附性和体外释药均较理想的处方。
Amphiphilic copolymer micelles play an important role in the field of drug delivery and their drug release behavior is strongly influenced by size and morphology of micelles.
两亲性共聚物胶束在药物控释方面有着重要应用，而胶束的尺寸形态与其药物传递行为密切相关。
Effects of formulation of drug layer, push layer and membrane on the release behavior of controlled release tablets were investigated and the optimal formulation was obtained.
考察含药层促渗聚合物、乳糖用量、助推层聚氧乙烯用量、助推层氯化钠用量及包衣液中含水量、醋酸纤维素浓度对释放度的影响，并对处方进行优化。
The factors which affect the lag time and drug release behavior were investigated, such as the thickness of the inner and outer layers, the amount of PVPP and other excipients, etc.
单因素考察发现，影响释药时滞和释药速率的主要因素为溶胀层中高效崩解剂比例、溶胀层增重及控释层增重。
The factors which affect the lag time and drug release behavior were investigated, such as the thickness of the inner and outer layers, the amount of PVPP and other excipients, etc.
单因素考察发现，影响释药时滞和释药速率的主要因素为溶胀层中高效崩解剂比例、溶胀层增重及控释层增重。
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