Jellyfish-Shaped Amphiphilic Dendrimers: Synthesis and Formation of Extremely Uniform Aggregates

被引:31
作者
Shao, Shiqun [1 ,2 ]
Si, Jingxing [1 ,2 ,3 ]
Tang, Jianbin [1 ,2 ]
Sui, Meihua [1 ,2 ]
Shen, Youqing [1 ,2 ]
机构
[1] Zhejiang Univ, Ctr Bionanoengn, Minist Educ, Key Lab Biomass Chem Engn, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Dept Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
[3] Zhejiang Univ, Sch Med, Dept Resp Med, Affiliated Hosp 2, Hangzhou 310009, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
BLOCK-COPOLYMERS; DRUG-DELIVERY; POLYMER; MICELLES; NANORODS; RELEASE;
D O I
10.1021/ma4025619
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Novel classes of jellyfish-shaped amphiphilic dendrimers composed of 7 hydrophilic poly(ethylene glycol) (PEG) arms and 14 hydrophobic polyester dendrons with beta-cyclodextrin (beta CD) as the core molecule were synthesized by a facile method. Seven PEG chains were first conjugated to the C-6 positions of native beta CD. Subsequently, dendritic polyester architectures were constructed from the remaining 14 secondary hydroxyl groups at C-2 and C-3 positions of the beta CD moiety, resulting in jellyfish-shaped amphiphilic dendrimers of different generations (7PEG-beta CD-Gx) with well-defined molecular structures. The amphiphilic dendrimers self-assembled into different morphologies dependent upon the hydrophilic fraction of the dendrimers, and very surprisingly, the fourth-generation dendrimers consisting of only several percent of PEG could form aggregates with extremely narrow size distributions.
引用
收藏
页码:916 / 921
页数:6
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