A unimolecular nanocapsule: Encapsulation property of amphiphilic polymer based on hyperbranched polythreitol

被引:88
作者
Kitajyo, Yoshikazu
Nawa, Yumiko
Tamaki, Masaki
Tani, Hirofumi
Takahashi, Kenji
Kaga, Harumi
Satoh, Toshifumi [1 ]
Kakuchi, Toyoji
机构
[1] Hokkaido Univ, Grad Sch Engn, Div Biotechnol & Macromol Chem, Sapporo, Hokkaido 6068628, Japan
[2] Kanazawa Univ, Grad Sch Nat Sci & Technol, Div Mat Chem, Kanazawa, Ishikawa 9201192, Japan
[3] Natl Inst Adv Ind Sci & Technol, Sapporo, Hokkaido 0628517, Japan
[4] Hokkaido Univ, CRIS, Div Innovat Res, Sapporo, Hokkaido 0010021, Japan
基金
日本学术振兴会;
关键词
amphiphiles; core-shell polymer; micelles;
D O I
10.1016/j.polymer.2007.06.026
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
Hyperbranched polythreitol (1) with different molecular weights (M-w,M-SLS: 1.18 x 10(4) and 4.79 x 10(4)) was reacted with trityl chloride in DMF to afford a novel amphiphilic polymer (2) consisting of 1 as the hydrophilic core and the trityl groups as the hydrophobic shell. Compound 2 was tested for its ability to act as a unimolecular nanocapsule toward the water-soluble dye, rose bengal (RB). Their encapsulation and release properties were also evaluated by comparison with the degree of substitution (DS) of the trityl groups, i.e., the hydrophobic shell density. The polymers were found to have very good unimolecular nanocapsule characteristics even at extremely low concentrations. The average number of RBs per polymer molecule depended on the hydrophilic core size and the hydrophobic shell density. The increasing DS value led to a decrease in the encapsulated amount due to the decrease in the hydrophilic core space, while the low DS value (less than ca. 20 mol%) led to a destabilization as a unimolecular nanocapsule and a lower encapsulation ability. In particular, 2 with ca. 23% DS value showed an efficient encapsulation. Based on a release test of the RB-loaded unimolecular nanocapsules, the polymers showed a high RB-holding ability in water. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4683 / 4690
页数:8
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