However, the use of nanoparticles for small molecular weight, water-soluble drugs has been limited by poor drug encapsulation efficiency and rapid release of the encapsulated drug.
然而，使用纳米粒包裹小分子量的水溶性药物，会受药物包囊效率低及包囊药物快速释放差的限制。
The process enables the preparation of microspheres having high drug encapsulation efficiency, almost not having a toxicity problem due to the residual solvent, and having good syringeability.
所述方法能够制备这样的微球：其具有高药物封装效率、几乎没有由于残余溶剂引起的毒性问 题并具有良好的可注射性。
The encapsulation efficiency and drug loading of triptolide-loaded poly (d, L-lactic acid) nanoparticles were analyzed by RP-HPLC and ultracentrifuge method in this study.
本文研究了反相高效液相色谱和超速冷冻离心测定雷公藤甲素聚乳酸纳米粒包封率和载药量的方法。
The solubility of CH331 in outer aqueous phase played a significant role in encapsulation efficiency and in vitro drug release of microspheres.
CH331在外水相中的溶解度影响微球的包封率和体外释药行为。
The drug loading rate, encapsulation efficiency, particle distribution and in vitro release of Lac-NCTD from liposomes were investigated, respectively.
考察了药物与磷脂的复合率，磷脂复合物脂质体的包封率，粒径大小和分布，以及体外释药特性。
OBJECTIVE To prepare the stable lipiodol double emulsion with uniform size and high encapsulation efficiency as drug carrier by a novel membrane emulsification technique.
目的采用新型微孔膜乳化法制备粒径均匀、包埋率高、包埋稳定的抗癌剂碘油复乳药物载体。
OBJECTIVE To prepare the stable lipiodol double emulsion with uniform size and high encapsulation efficiency as drug carrier by a novel membrane emulsification technique.
目的采用新型微孔膜乳化法制备粒径均匀、包埋率高、包埋稳定的抗癌剂碘油复乳药物载体。
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