Objective To prepare a harmine hydrochloride liposome formulation with high encapsulation efficiency.
目的制备高包封率的盐酸去氢骆驼蓬碱脂质体。
The encapsulation efficiency of PGS liposomes were determined by high performance gel permeation chromatography (HPGPC).
采用高效凝胶渗透色谱法(HPGPC)测定古糖酯脂质体的包封率。
CONCLUSION Reverse-phase evaporation is suitable to prepare PGS liposomes with high encapsulation efficiency and small vesicles.
结论反相蒸发法制备的古糖酯脂质体包封率高，粒径小，形态稳定。
This paper examines these technological factors on particle size and encapsulation efficiency of microspheres and other properties;
本文研究了这些工艺因素对微球粒径和包封率等性能的影响；
Conclusion Double emulsification and freeze-thawing method can significantly increase the encapsulation efficiency 5-FU in liposomes.
结论二次乳化法和冻融法结合能显著提高5-氟尿嘧啶脂质体的包封率。
CONCLUSION the method was proved to be stable and reliable to determine the encapsulation efficiency of biodegradable PLGA microspheres.
结论此方法稳定、可靠，可以满足生物可降解微球包封率测定的要求。
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。
CONCLUSION the liposomes were prepared with good encapsulation efficiency and stability, and the preparation was simple, feasible and replicable.
结论蜂毒多肽长循环脂质体包封率、稳定性较高，且制备工艺简单、重现性好。
Then mini column centrifugation method was adopted to determine the encapsulation efficiency (EE) before and after curcumin liposomes being coated.
采用微柱离心法测定姜黄素脂质体包衣前后包封率的变化。
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。
It was found that microcapsules with gelatin-gum Arabic as wall material had smooth surface, superior transparence and encapsulation efficiency high to 91.2%.
经过研究发现，以明胶-阿拉伯胶为壁材得到的微胶囊，囊壁光滑、透明性好，对芯材包封率高，达到91.2%。
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。
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 properties of viscosity and surface activity of urea-formaldehyde oligomers were studied, as well as their relationship with the encapsulation efficiency of microcapsules.
研究了低分子量脲甲醛缩聚物水溶液的粘度特征和表面活性及其与胶囊包封率的关系。
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。
Higher feed ratio could lead to higher loading capacity and lower encapsulation efficiency under the same degree of substitution of cholesteryl moiety and molecular weights of parent pullulan.
当取代度和相对分子质量相同时，随着投料比的增加，载药量增加而包封率降低。
The optimized formulation of aconitine ethosome is high in encapsulation efficiency and good in stability, and the anti-inflammatory and analgesic activity of aconitine ethosome was significant.
以优化工艺制得的乌头碱醇质体包封率较高、稳定性好，且具有良好的抗炎镇痛作用。
The optimized formulation of aconitine ethosome is high in encapsulation efficiency and good in stability, and the anti-inflammatory and analgesic activity of aconitine ethosome was significant.
以优化工艺制得的乌头碱醇质体包封率较高、稳定性好，且具有良好的抗炎镇痛作用。
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