Locally Controlled Diffusive Release of Bone Morphogenetic Protein-2 Using Micropatterned Gelatin Methacrylate Hydrogel Carriers

被引:21
|
作者
Yi, Myong-Hee [1 ]
Lee, Ji-Eun [2 ]
Kim, Chang-Beom [3 ]
Lee, Keun-Woo [1 ]
Lee, Kwang-Ho [4 ]
机构
[1] Yonsei Univ, Dept Prosthodont, Coll Dent, Seoul 03722, South Korea
[2] Kangwon Natl Univ, Grad Program Adv Funct Mat & Devices Dev, Chunchon 24341, South Korea
[3] Elect & Telecommun Res Inst, Intelligent Robot Res Team, Daejeon 34129, South Korea
[4] Kangwon Natl Univ, Div Mech & Biomed Mechatron & Mat Sci & Engn, Chunchon 24341, South Korea
基金
新加坡国家研究基金会;
关键词
Bone generation; Gelatin-methacrylate; Localized release; Controlled release; Bone morphogenetic protein-2; OSTEOGENIC DIFFERENTIATION; DRUG-DELIVERY; STEM-CELLS; REGENERATION; SCAFFOLDS; BMP-2; POLYCAPROLACTONE; FABRICATION; NANOFIBERS; MARROW;
D O I
10.1007/s13206-020-4411-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, a novel and simple bone morphogenetic protein (BMP)-2 carrier is developed, which enables localized and controlled release of BMP-2 and facilitates bone regeneration. BMP-2 is localized in the gelatin methacrylate (GelMA) micropatterns on hydrophilic semi-permeable membrane (SNM), and its controlled release is regulated by the concentration of GelMA hydrogel and BMP-2. The controlled release of BMP-2 is verified using computational analysis and quantified using fluorescein isothiocyanate-bovine serum albumin (FITC-BSA) diffusion model. The osteogenic differentiation of osteosarcoma MG-63 cells is manipulated by localized and controlled BMP-2 release. The calcium deposits are significantly higher and the actin skeletal networks are denser in MG-63 cells cultured in the BMP-2-immobilized GelMA micropattern than in the absence of BMP-2. The proposed BMP-2 carrier is expected to not only act as a barrier membrane that can prevent invasion of connective tissue during bone regeneration, but also as a carrier capable of localizing and controlling the release of BMP-2 due to GelMA micropatterning on SNM. This approach can be extensively applied to tissue engineering, including the localization and encapsulation of cells or drugs.
引用
收藏
页码:405 / 420
页数:16
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