文献摘要信息 .22mv,最大饱和磁化强度为56.2emu/g,醛基化海藻酸钠的氧化程度为21.78±0.98％,顺铂的包封率(drug encapsulation efficiency,DEE)为49.05±1.58％,载药量(drug loading efficiency,DLE)为14.3
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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。
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