Considered the application in nanomedicine, the effect of the diverse morphologies on drug loading efficiency was also investigated.
同时，不同形貌的聚醚-聚酸酐三元共聚物胶束在载药效率和载药量上有明显差别。
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。
Optimization of preparation and formulation was accomplished by evaluating the drug-loading amounts and the entrapment efficiency of luteolin liposomes.
方法采用薄膜分散法和冻干工艺进行木犀草素脂质体制备，并以载药量、包封率为评价指标，优化制备处方和工艺。
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。
Conclusion: The HCPT-SSLN has high entrapment efficiency and drug loading, uniform particle size, good stability, which initially indicates that HCPT is fit for being incorporated into SSLN.
结论：本实验制备的HCPT - SSLN包封率和载药量较高，粒径分布均匀，稳定性良好。初步表明HCPT适合进行SSLN包裹。
Besides, from the view of the efficiency of drug release, the higher content of the drug loading, the more the drug residues in the nano-tubes relatively.
同时，从药物最终的释放效率来看，载药量越高，纳米管中的药物残留也相对越多。
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。
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。
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。
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