Injectable Hydrogels from Segmented PEG-Bisurea Copolymers

被引:47
|
作者
Pawar, Gajanan M. [1 ,2 ]
Koenigs, Marcel [1 ,2 ]
Fahimi, Zahra [2 ,3 ]
Cox, Martijn [4 ]
Voets, Ilja K. [1 ,2 ]
Wyss, Hans M. [2 ,3 ]
Sijbesma, Rint P. [1 ,2 ]
机构
[1] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Inst Complex Mol Syst, NL-5600 MB Eindhoven, Netherlands
[3] Eindhoven Univ Technol, Dept Mech Engn, NL-5600 MB Eindhoven, Netherlands
[4] Xeltis BV, Eindhoven, Netherlands
关键词
POLY(ETHYLENE GLYCOL) HYDROGELS; BIS-UREA COMPOUNDS; PEPTIDE HYDROGELS; COPOLY(ETHER UREA)S; DELIVERY; BEHAVIOR; DESIGN; WATER; ENCAPSULATION; MORPHOLOGY;
D O I
10.1021/bm301242v
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe the preparation of an injectable, biocompatible, and elastic segmented copolymer hydrogel for biomedical applications, with segmented hydrophobic bisurea hard segments and hydrophilic PEG segments. The segmented copolymers were obtained by the step growth polymerization of amino-terminated PEG and aliphatic diisocyanate. Due to their capacity for multiple hydrogen bonding within the hydrophobic segments, these copolymers can form highly stable gels in water at low concentrations. Moreover, the gels show shear thinning by a factor of 40 at large strain, which allows injection through narrow gauge needles. Hydrogel moduli are highly tunable via the physical cross-link density and the length of the hydrophilic segments. In particular, the mechanical properties can be optimized to match the properties of biological host tissues such as muscle tissue and the extracellular matrix.
引用
收藏
页码:3966 / 3976
页数:11
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