Influence of cross-linker chemistry on release kinetics of PEG-co-PGA hydrogels

被引:42
作者
Bencherif, Sidi A. [1 ]
Sheehan, Jeffrey A. [2 ]
Hollinger, Jeffrey O. [3 ,4 ]
Walker, Lynn M. [2 ]
Matyjaszewski, Krzysztof [1 ]
Washburn, Newell R. [1 ,4 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Bone Tissue Engn Ctr, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
关键词
PEG-co-PGA; hydrogels; cross-linker; controlled release; DNA; MECHANICAL-PROPERTIES; MOLECULAR-WEIGHT; DRUG-DELIVERY; DNA DELIVERY; NETWORKS; DEGRADATION; BEHAVIOR; EROSION;
D O I
10.1002/jbm.a.32069
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
An investigation of encapsulated plasmid [DNA release from degradable poly(ethylene glycol)-co-poly(glycolic colic acid) hydrogels (PEG-co-PGA) is presented. We determined by varying the chemistry of the cross-linker group, significant variations in hydrogel degradation kinetics could be achieved to control the release profiles of plasmid DNA. We prepared three analogues of PEG-co-PGA hydrogels by a photopolymerization process and measured variation in degradation rates by monitoring mechanical properties and release of plasmid DNA. H-1 1D DOSY NMR (one-dimensional diffusion ordered nuclear magnetic resonance spectroscopy) was used to measure conversion of vinyl groups after photocross-linking. Nearly full vinyl conversion was reached after 10 min exposure Under Ultraviolet light. Gel electrophoresis analysis confirmed that plasmid DNA remained structurally intact after photoencapsulation and release. from the gels. This approach provides art additional strategy for controlling the release of biologically, active compounds from hydrogels. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 90A: 142-153, 2009
引用
收藏
页码:142 / 153
页数:12
相关论文
共 28 条
[1]   Regulating bone formation via controlled scaffold degradation [J].
Alsberg, E ;
Kong, HJ ;
Hirano, Y ;
Smith, MK ;
Albeiruti, A ;
Mooney, DJ .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (11) :903-908
[2]   Photopolymerization kinetics of multifunctional monomers [J].
Andrzejewska, E .
PROGRESS IN POLYMER SCIENCE, 2001, 26 (04) :605-665
[3]   Mechanical properties of hydrogels and their experimental determination [J].
Anseth, KS ;
Bowman, CN ;
BrannonPeppas, L .
BIOMATERIALS, 1996, 17 (17) :1647-1657
[4]   Delivery of osteoinductive growth factors from degradable PEG hydrogels influences osteoblast differentiation and mineralization [J].
Burdick, JA ;
Mason, MN ;
Hinman, AD ;
Thorne, K ;
Anseth, KS .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (01) :53-63
[5]   Photoinitiated crosslinked degradable copolymer networks for tissue engineering applications [J].
Davis, KA ;
Burdick, JA ;
Anseth, KS .
BIOMATERIALS, 2003, 24 (14) :2485-2495
[6]   Robust and prolonged gene expression from injectable polymeric implants [J].
Eliaz, RE ;
Szoka, FC .
GENE THERAPY, 2002, 9 (18) :1230-1237
[7]   Statistical mechanics of cross-linked polymer networks I Rubberlike elasticity [J].
Flory, PJ ;
Rehner, J .
JOURNAL OF CHEMICAL PHYSICS, 1943, 11 (11) :512-520
[8]  
FLORY PJ, 1953, RPINCIPLES POLYM CHE, P464
[9]   THE CLINICAL EFFICACY OF POLY(ETHYLENE GLYCOL)-MODIFIED PROTEINS [J].
FUERTGES, F ;
ABUCHOWSKI, A .
JOURNAL OF CONTROLLED RELEASE, 1990, 11 (1-3) :139-148
[10]   MODELING OF POLYMER EROSION [J].
GOPFERICH, A ;
LANGER, R .
MACROMOLECULES, 1993, 26 (16) :4105-4112