Drug-loading

基本解釋

And pH gradient active drug loading method was employed to improve the DEE of INT liposome.
通過pH梯度主動(dòng)載藥法提高脂質(zhì)體的包封率;
Thirdly, the drug loading and leasing ratio of P(NIPAm-co-AAm) and PAAc/P(NIPAm-co-AAm) gels was studied.
研究了組分配比對(duì)P(NIPAm-co-AAm)和PAAc/P(NIPAm-co-AAm)凝膠的載藥和釋藥率的影響。
The entrapment efficiency in cationic liposomes was in the same range even if the drug loading was increased.
即使填充藥量增加，帶有陽離子的脂質(zhì)體的包封率（仍處于相同范圍）沒有變化。
All these microspheres showed a restively higher drug loading efficiency at a pH value of about 7.
該制備方法具有一定的普適性，利用該方法可以制備各種無機(jī)粒子為核有機(jī)聚合物為殼的復(fù)合微球，無機(jī)粒子可以是其它金屬（或其合金）或金屬氧化物粒子，通過在其表面覆蓋二氧化硅并進(jìn)一步用硅烷偶聯(lián)修飾，通過單體的沉淀聚合可以制得復(fù)合微球，殼層聚合物不限于聚（N-異丙基丙烯酰胺），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.
結(jié)論制備的多西他賽納米脂質(zhì)載體粒徑小，藥物包封率高，并可實(shí)現(xiàn)藥物控釋。