Clinical translation of controlled protein delivery systems for tissue engineering

被引:34
|
作者
Spiller, Kara L. [1 ]
Vunjak-Novakovic, Gordana [1 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10032 USA
关键词
Tissue engineering; Scaffolds; Protein delivery; Translation; Regulatory pathways; BONE MORPHOGENETIC PROTEIN-2; ENDOTHELIAL GROWTH-FACTOR; OPEN TIBIAL FRACTURES; PROTEIN-2/COMPRESSION RESISTANT MATRIX; POSTEROLATERAL LUMBAR FUSION; FUMARATE) HYDROGEL SCAFFOLDS; CORONARY-ARTERY DISEASE; MESENCHYMAL STEM-CELLS; SIZE DEFECT MODEL; IN-VITRO RELEASE;
D O I
10.1007/s13346-013-0135-1
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Strategies that utilize controlled release of drugs and proteins for tissue engineering have enormous potential to regenerate damaged organs and tissues. The multiple advantages of controlled release strategies merit overcoming the significant challenges to translation, including high costs and long, difficult regulatory pathways. This review highlights the potential of controlled release of proteins for tissue engineering and regenerative medicine. We specifically discuss treatment modalities that have reached preclinical and clinical trials, with emphasis on controlled release systems for bone tissue engineering, the most advanced application with several products already in clinic. Possible strategies to address translational and regulatory concerns are also discussed.
引用
收藏
页码:101 / 115
页数:15
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