Control Growth Factor Release Using a Self-Assembled [polycation:heparin] Complex

被引:40
作者
Zern, Blaine J.
Chu, Hunghao
Wang, Yadong
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Inst Bioengn & Biosci, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
FACTOR DELIVERY; SUSTAINED-RELEASE; HEPARIN; HYDROGELS; BINDING; MATRICES; SCAFFOLDS; PEPTIDES; AFFINITY; GELS;
D O I
10.1371/journal.pone.0011017
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The importance of growth factors has been recognized for over five decades; however their utilization in medicine has yet to be fully realized. This is because free growth factors have short half-lives in plasma, making direct injection inefficient. Many growth factors are anchored and protected by sulfated glycosaminoglycans in the body. We set out to explore the use of heparin, a well-characterized sulfated glycosaminoglycan, for the controlled release of fibroblast growth factor-2 (FGF-2). Heparin binds a multitude of growth factors and maintains their bioactivity for an extended period of time. We used a biocompatible polycation to precipitate out the [heparin: FGF-2] complex from neutral buffer to form a release matrix. We can control the release rate of FGF-2 from the resultant matrix by altering the molecular weight of the polycation. The FGF-2 released from the delivery complex maintained its bioactivity and initiated cellular responses that were at least as potent as fresh bolus FGF-2 and fresh heparin stabilized FGF-2. This new delivery platform is not limited to FGF-2 but applicable to the large family of heparin-binding growth factors.
引用
收藏
页数:7
相关论文
共 37 条
[1]  
Alberts B., 2002, The shape and structure of proteins, Vfourth, DOI 10.1093/aob/mcg023
[2]   Heparin functionalized PEG gels that modulate protein adsorption for hMSC adhesion and differentiation [J].
Benoit, DSW ;
Anseth, KS .
ACTA BIOMATERIALIA, 2005, 1 (04) :461-470
[3]   Stimulation of neurite outgrowth by neurotrophins delivered from degradable hydrogels [J].
Burdick, JA ;
Ward, M ;
Liang, E ;
Young, MJ ;
Langer, R .
BIOMATERIALS, 2006, 27 (03) :452-459
[4]   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
[5]  
CARPENTER G, 1990, J BIOL CHEM, V265, P7709
[6]   Development of poly-(D,L-lactide-coglycolide) microsphere formulations containing recombinant human vascular endothelial growth factor to promote local angiogenesis [J].
Cleland, JL ;
Duenas, ET ;
Park, A ;
Daugherty, A ;
Kahn, J ;
Kowalski, J ;
Cuthbertson, A .
JOURNAL OF CONTROLLED RELEASE, 2001, 72 (1-3) :13-24
[7]   Endothelial cells and VEGF in vascular development [J].
Coultas, L ;
Chawengsaksophak, K ;
Rossant, J .
NATURE, 2005, 438 (7070) :937-945
[8]   Heparin structure and interactions with basic fibroblast growth factor [J].
Faham, S ;
Hileman, RE ;
Fromm, JR ;
Linhardt, RJ ;
Rees, DC .
SCIENCE, 1996, 271 (5252) :1116-1120
[9]   Biodegradable elastomeric scaffolds with basic fibroblast growth factor release [J].
Guan, Jianjun ;
Stankus, John J. ;
Wagner, William R. .
JOURNAL OF CONTROLLED RELEASE, 2007, 120 (1-2) :70-78
[10]   INSULIN-LIKE GROWTH FACTOR-I AND FACTOR-II IN HEALTHY MAN - ESTIMATIONS OF HALF-LIVES AND PRODUCTION-RATES [J].
GULER, HP ;
ZAPF, J ;
SCHMID, C ;
FROESCH, ER .
ACTA ENDOCRINOLOGICA, 1989, 121 (06) :753-758