药物输送
毒品携带者
芯(光纤)
材料科学
壳体(结构)
药品
纳米技术
医学
药理学
复合材料
作者
Peng Zhao,Lixin Liu,Xiaoqin Feng,Chun Wang,Xintao Shuai,Yongming Chen
标识
DOI:10.1002/marc.201200172
摘要
Abstract Core/shell wormlike polymer brushes with densely grafted poly( ϵ ‐caprolactone)‐ b ‐poly(ethylene oxide) (PCL‐ b ‐PEO) are synthesized via grafting an alkynyl terminated PCL‐ b ‐PEO (ay‐PCL 17 ‐ b ‐PEO 113 ) onto a well‐defined azido functionalized polymethacrylate (PGA 940 ) and are evaluated preliminarily as a single molecular cylindrical vehicle for drug delivery. Water soluble molecular worms of ca. 230 nm are obtained and then the anticancer drug doxorubicin (DOX) is loaded into its PCL core by hydrophobic interaction. Compared with spherical micelles from linear PCL 17 ‐ b ‐PEO 113 , the brushes demonstrate a lower loading efficiency but a faster release rate of DOX. Confocal laser scanning microscopy measurements show that DOX‐loaded cylindrical molecular brushes can easily enter into HeLa and HepG2 cells in 1 h.
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