pH-triggered self-assembly of biocompatible histamine-functionalized triblock copolymers

被引:54
|
作者
Lundberg, Pontus [1 ]
Lynd, Nathaniel A. [1 ]
Zhang, Yuning [2 ]
Zeng, Xianghui [2 ]
Krogstad, Daniel V. [1 ]
Paffen, Tim [1 ]
Malkoch, Michael [3 ]
Nystrom, Andreas M. [2 ]
Hawker, Craig J. [1 ,4 ,5 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[2] Karolinska Inst, Dept Neurosci, Swedish Med Nanosci Ctr, SE-17177 Stockholm, Sweden
[3] KTH Royal Inst Technol, Sch Chem Sci & Engn, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
[4] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[5] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会; 美国国家卫生研究院; 瑞典研究理事会;
关键词
DRUG-DELIVERY; HYDROGELS; GELS; POLYMER; THERAPEUTICS; PROTEINS; BIOLOGY; DRIVEN; CANCER;
D O I
10.1039/c2sm26996a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Histamine functionalized poly(allyl glycidyl ether)-b-poly(ethylene glycol)-b-poly(allyl glycidyl ether) (PAGE-PEO-PAGE) triblock copolymers represent a new class of physically cross-linked, pH-responsive hydrogels with significant potential for biomedical applications. These telechelic triblock copolymers exhibited abrupt and reversible hydrogelation above pH 7.0 due to a hydrophilic/hydrophobic transition of the histamine units to form a network of hydrophobic domains bridged by a hydrophilic PEO matrix. These hydrophobic domains displayed improved ordering upon increasing pH and self-assembled into a body centered cubic lattice at pH 8.0, while at lower concentrations formed well-defined micelles. Significantly, all materials were found to be non-toxic when evaluated on three different cell lines and suggests a range of medical and biomedical applications.
引用
收藏
页码:82 / 89
页数:8
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