Nanostructuring of PEG-fibrinogen polymeric scaffolds

被引:32
作者
Frisman, Ilya [1 ]
Seliktar, Dror [2 ,3 ]
Bianco-Peled, Havazelet [1 ,3 ]
机构
[1] Technion Israel Inst Technol, Dept Chem Engn, IL-32000 Haifa, Israel
[2] Technion Israel Inst Technol, Dept Biomed Engn, IL-32000 Haifa, Israel
[3] Technion Israel Inst Technol, Russell Berrie Nanotechnol Inst, IL-32000 Haifa, Israel
关键词
Scaffold; Nanostructuring; PEGylation; Poly(ethylene glycol); Fibrinogen; TRIBLOCK COPOLYMERS; HYDROGEL SCAFFOLDS; AQUEOUS-SOLUTIONS; PROTEIN; DELIVERY; MATRICES;
D O I
10.1016/j.actbio.2009.07.015
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recent studies have shown that nanostructuring of scaffolds for tissue engineering has a major impact on their interactions with cells. The current investigation focuses on nanostructuring of a biocompatible, biosynthetic polymeric hydrogel scaffold made from crosslinked poly(ethylene glycol)-fibrinogen conjugates. Nanostructuring was achieved by the addition of the block copolymer Pluronic (R) F127, which self-assembles into nanometric micelles at certain concentrations and temperatures. Cryo-transmission electron microscopy experiments detected F127 micelles, both embedded within PEGylated fibrinogen hydrogels and in solution. The density of the F127 micelles, as well as their ordering, increased with increasing block copolymer concentration. The mechanical properties of the nanostructured hydrogels were investigated using stress-sweep rheological testing. These tests revealed a correlation between the block copolymer concentration and the storage modulus of the composite hydrogels. In vitro cellular assays confirmed that the increased modulus of the hydrogels did not limit the ability of the cells to form extensions and become spindled within the three-dimensional (3-D) hydrogel culture environment. Thus, altering the nanostructure of the hydrogel may be used as a strategy to control cellular behavior in 3-D through changes in mechanical properties of the environment. (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2518 / 2524
页数:7
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