drug entrapment efficiency

基本解释

Aim To prepare integerrimine (INT ) liposomes with high drug entrapment efficiency ( DEE ) and good stability and then make them into liposomal gel.
目的制备具有高包封率和良好稳定性的全缘千里光碱（INT）脂质体，并将其制成凝胶剂。
The results indicated that the microspheres had poor drug loading and entrapment efficiency abilities due to residual impurities contained in polymer.
初步分析表明，因聚合物中残留的微小杂质的影响，造成了所制备的载药微球过低的载药量及包封率。
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The drug loading, entrapment efficiency, diameter of nanoparticles and particle diameter distribution, shape and release curve of nanoparticles were investigated in vitro.
对纳米粒的载药量、大小及分布、形态及体外释放等进行了研究。
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药物包封率
The NLC exhibited improved drug entrapment efficiency and drug loading capacity by increasing OA content. The in vitro drug release rates were enhanced with the increasing of OA content.
随着油酸含量的增加,NLC的药物包封率、载药量、药物释放速率随之增加。
化学
药物包封率
To overcome the disadvantages such as lower drug entrapment efficiency (EE) and loading (DL) of lipid nanospheres prepared by conventional solvent diffusion method, a solvent diffusion method in drug saturated aqueous system was developed.
为了克服采用传统溶剂扩散法制备脂质纳米粒存在的药物包封率与载药量较低等缺点,研究出一种新的溶剂扩散法。新的溶剂扩散法采用外相为药物饱和溶液系统。