Production of heparin-functionalized hydrogels for the development of responsive and controlled growth factor delivery systems

被引:199
作者
Nie, Ting
Baldwin, Aaron
Yamaguchi, Nori
Kiick, Kristi L.
机构
[1] Univ Delaware, Dept Mat Sci & Engn, Newark, DE 19716 USA
[2] Delaware Biotechnol Inst, Newark, DE 19711 USA
关键词
hepatin; hydrogel; growth factor; controlled release; protein release;
D O I
10.1016/j.jconrel.2007.04.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methods to assemble polymeric hydrogels on the basis of noncovalent protein-glycosaminoglycan interactions have been previously demonstrated by us and others and hold promise in the development of receptor-responsive hydrogel materials; improvements in the mechanical properties of such systems would broaden their utility. Thus, in situ crosslinkable and degradable heparin-containing hydrogels were designed for the binding and controlled release of growth factors. Specifically, maleimide-functionalized high molecular weight heparin (HMWH) was synthesized via straightforward chemical methods that permitted facile and controllable modification of carboxylates in HMWH with maleimide groups via control of catalyst and reaction conditions, as assessed via H-1 NMR spectroscopy. These modified heparins were crosslinked into hydrogels via reaction with various thiol-functionalized PEGs. The gelation times and elastic moduli of the gels, as assessed through oscillatory rheometry, could be tuned by controlling the functionality of HMWH, the concentration of the hydrogel, the identity of the PEG-based crosslinker, as well as the molar ratio between maleimide and thiol groups. The capability of the hydrogels to bind to growth factors was investigated with immunochemical assays. Preliminary studies indicate the controlled release of basic fibroblast growth factor (bFGF) from these materials and suggest their broader use in the design of responsive materials. (c) 2007 Elsevier B.V All rights reserved.
引用
收藏
页码:287 / 296
页数:10
相关论文
共 49 条
[1]   POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) BLOCK-COPOLYMER SURFACTANTS IN AQUEOUS-SOLUTIONS AND AT INTERFACES - THERMODYNAMICS, STRUCTURE, DYNAMICS, AND MODELING [J].
ALEXANDRIDIS, P ;
HATTON, TA .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1995, 96 (1-2) :1-46
[2]   Photoscissable hydrogel synthesis via rapid photopolymerization of novel PEG-based polymers in the absence of photoinitiators [J].
Andreopoulos, FM ;
Deible, CR ;
Stauffer, MT ;
Weber, SG ;
Wagner, WR ;
Beckman, EJ ;
Russell, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (26) :6235-6240
[3]  
Baskar C, 1999, J AM OIL CHEM SOC, V76, P853
[4]   Rational design of hydrogels for tissue engineering: Impact of physical factors on cell behavior [J].
Brandl, Ferdinand ;
Sommer, Florian ;
Goepferich, Achim .
BIOMATERIALS, 2007, 28 (02) :134-146
[5]   Injectable glycosaminoglycan hydrogels for controlled release of human basic fibroblast growth factor [J].
Cai, SS ;
Liu, YC ;
Shu, XZ ;
Prestwich, GD .
BIOMATERIALS, 2005, 26 (30) :6054-6067
[6]  
Capila I, 2002, ANGEW CHEM INT EDIT, V41, P391
[7]   Action of microparticles of heparin and alginate crosslinked gel when used as injectable artificial matrices to stabilize basic fibroblast growth factor and induce angiogenesis by controlling its release [J].
Chinen, N ;
Tanihara, M ;
Nakagawa, M ;
Shinozaki, K ;
Yamamoto, E ;
Mizushima, Y ;
Suzuki, Y .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 67A (01) :61-68
[8]   Cross-linking of dermal sheep collagen using a water-soluble carbodiimide [J].
Damink, LHHO ;
Dijkstra, PJ ;
vanLuyn, MJA ;
vanWachem, PB ;
Nieuwenhuis, P ;
Feijen, J .
BIOMATERIALS, 1996, 17 (08) :765-773
[9]   Hydrogels for tissue engineering: scaffold design variables and applications [J].
Drury, JL ;
Mooney, DJ .
BIOMATERIALS, 2003, 24 (24) :4337-4351
[10]   Conjugate addition reactions combined with free-radical cross-linking for the design of materials for tissue engineering [J].
Elbert, DL ;
Hubbell, JA .
BIOMACROMOLECULES, 2001, 2 (02) :430-441