胶束
聚乙二醇
化学
阿霉素
粒径
PEG比率
纳米载体
色谱法
核化学
生物物理学
药物输送
有机化学
水溶液
生物
遗传学
物理化学
经济
化疗
财务
作者
Yuran Liu,Ji Wu,Long Huang,Qiao Jin,Ning Wang,Di Yu,Guangyuan Zhang,Shangmin Yu,Qingxiang Guan
标识
DOI:10.1016/j.ijbiomac.2020.03.136
摘要
To evaluate if mixed micelles of [email protected]/TPGS can allow for the superior antitumor efficiency than [email protected] micelles. The complex of doxorubicin (Dox) and sodium cholate was encapsulated into the mixed micelles composed of folate-mediated stearic acid-modified Bletilla striata polysaccharide (FA-BSP-SA) and D-α-tocopheryl polyethylene glycol succinate (TPGS). Its average particle size increased whereas load capacity (LC) and encapsulation efficiency (EE) decreased with the increase of TPGS mass ratio in the mixed micelles. The changes of morphology, particle size and doxorubicin release in vitro demonstrated the pH sensitivity of micelles. FA-BSP-SA/TPGS mixed micelle exhibited average particle size of 147.3 nm, LC of 14.4% and EE of 91.9% for doxorubicin at the weight ratio of 3: 1. The doxorubicin release rate of micelles was faster in pH 5.0 media compared with that in pH 6.0 and 7.4 media. The cytotoxicity in vitro and antitumor efficacy in vivo results of [email protected]/TPGS micelle were more superior to that of free doxorubicin and [email protected] single micelle. For [email protected]/TPGS micelle, the clathrin-mediated endocytosis was the dominant mechanism of intracellular uptake. The FA-BSP-SA/TPGS mixed micelle may be a promising drug delivery system for cancer chemotherapy.
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