Designing Bioactive Delivery Systems for Tissue Regeneration

被引:31
作者
Davis, Hillary E. [1 ,2 ]
Leach, J. Kent [1 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, Sacramento, CA 95817 USA
关键词
Recombinant proteins; Growth factors; Delivery vehicles; Diffusion; Hydrogels; Microspheres; Scaffolds; Tissue engineering; GROWTH-FACTOR DELIVERY; BONE MORPHOGENETIC PROTEIN-2; QUANTIFYING DRUG-RELEASE; IN-VITRO RELEASE; MATHEMATICAL-MODEL; POLY(LACTIDE-CO-GLYCOLIDE) MICROPARTICLES; MULTIPHOTON MICROSCOPY; ALGINATE MICROSPHERES; POLY(ETHYLENE GLYCOL); SEQUENTIAL DELIVERY;
D O I
10.1007/s10439-010-0135-y
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The direct infusion of macromolecules into defect sites generally does not impart adequate physiological responses. Without the protection of delivery systems, inductive molecules may likely redistribute away from their desired locale and are vulnerable to degradation. In order to achieve efficacy, large doses supplied at interval time periods are necessary, often at great expense and ensuing detrimental side effects. The selection of a delivery system plays an important role in the rate of re-growth and functionality of regenerating tissue: not only do the release kinetics of inductive molecules and their consequent bioactivities need to be considered, but also how the delivery system interacts and integrates with its surrounding host environment. In the current review, we describe the means of release of macromolecules from hydrogels, polymeric microspheres, and porous scaffolds along with the selection and utilization of bioactive delivery systems in a variety of tissue-engineering strategies.
引用
收藏
页码:1 / 13
页数:13
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