Star-Shaped Polypeptide/Glycopolymer Biohybrids: Synthesis, Self-Assembly, Biomolecular Recognition, and Controlled Drug Release Behavior

被引:43
|
作者
Qiu, Shuo [1 ]
Huang, Hui [1 ]
Dai, Xia-Hu [1 ]
Zhou, Wei [1 ]
Dong, Chang-Ming [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Technol, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
biohybrids; biomaterials; drug delivery systems; nanoparticles; polypeptide/glycopolymer; self-assembly; targeted drug delivery; MULTIPLE MORPHOLOGIES; MULTIVALENT LIGANDS; DIBLOCK COPOLYMERS; PEPTIDE-SYNTHESIS; BLOCK-COPOLYMERS; NANOPARTICLES; POLYMERIZATION; ARCHITECTURE; GELATION; SYSTEMS;
D O I
10.1002/pola.23301
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Star-shaped polypeptide/glycopolymer biohybrids composed of poly(gamma-benzyl L-glutamate) and poly(D-gluconamidoethyl methacrylate), exhibiting controlled molecular weights and low polydispersities, were synthesized by the combination of ring-opening polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride and the direct atom transfer radical polymerization of unprotected D-gluconamidoethyl methacrylate glycomonomer. These biohybrids were characterized in detail by means of FTIR, H-1 NMR, gel permeation chromatography, differential scanning calorimetry, and wide angle X-ray diffraction. Independent of weight fraction of hydrophilic glycopolymer segment, the biohybrids self-assembled into large spherical micelles in aqueous solution, which had a helical polypeptide core surrounded by a multivalent glycopolymer shell. The deprotected poly(L-glutamate)/glycopolymer hybrid exhibited a pH-sensitive self-assembly behavior, and the average size of the nanoparticles decreased gradually over the aqueous pH value. Moreover, whatever these biohybrids existed in unimolecular level or glycopolymer-surfaced nanoparticles, they had specific biomolecular recognition with Concanavalin A compared with bovine serum albumin. Furthermore, star-shaped biohybrids showed a higher doxorubicin loading efficiency and longer drug-release time than linear analogues. This potentially provides a platform for fabricating targeted anticancer drug delivery system and studying glycoprotein functions in vitro. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2009-2023, 2009
引用
收藏
页码:2009 / 2023
页数:15
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