Drug-loading

基本解释

And pH gradient active drug loading method was employed to improve the DEE of INT liposome.
通过pH梯度主动载药法提高脂质体的包封率;
Thirdly, the drug loading and leasing ratio of P(NIPAm-co-AAm) and PAAc/P(NIPAm-co-AAm) gels was studied.
研究了组分配比对P(NIPAm-co-AAm)和PAAc/P(NIPAm-co-AAm)凝胶的载药和释药率的影响。
The entrapment efficiency in cationic liposomes was in the same range even if the drug loading was increased.
即使填充药量增加，带有阳离子的脂质体的包封率（仍处于相同范围）没有变化。
All these microspheres showed a restively higher drug loading efficiency at a pH value of about 7.
该制备方法具有一定的普适性，利用该方法可以制备各种无机粒子为核有机聚合物为壳的复合微球，无机粒子可以是其它金属（或其合金）或金属氧化物粒子，通过在其表面覆盖二氧化硅并进一步用硅烷偶联修饰，通过单体的沉淀聚合可以制得复合微球，壳层聚合物不限于聚（N-异丙基丙烯酰胺），也可以是其它聚合物。
Conclusions Docetaxel-NLC with small particle sizes has improved drug loading capacity and controlled drug release properties.
结论制备的多西他赛纳米脂质载体粒径小，药物包封率高，并可实现药物控释。