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Fabrication of a BMP-2-immobilized porous microsphere modified by heparin for bone tissue engineering

Authors
Kim, Sung EunYun, Young-PilShim, Kyu-SikPark, KyeongsoonChoi, Sung-WookShin, Dong HyupSuh, Dong Hun
Issue Date
1-10월-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Bone morphogenic protein-2 (BMP-2); Porous microspheres; Fluidic device; Heparin; Bone tissue engineering
Citation
COLLOIDS AND SURFACES B-BIOINTERFACES, v.134, pp.453 - 460
Indexed
SCIE
SCOPUS
Journal Title
COLLOIDS AND SURFACES B-BIOINTERFACES
Volume
134
Start Page
453
End Page
460
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/92228
DOI
10.1016/j.colsurfb.2015.05.003
ISSN
0927-7765
Abstract
The purpose of this study was to fabricate BMP-2-immobilized porous poly(lactide-co-glycolide) (PLGA) microspheres (PMS) modified with heparin for bone regeneration. A fluidic device was used to fabricate PMS and the fabricated PMS was modified with heparin-dopamine (Hep-DOPA). Bone morphogenic protein-2 (BMP-2) was immobilized on the heparinized PMS (Hep-PMS) via electrostatic interactions. Both PMS and modified PMS were characterized using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). MG-63 cell activity on PMS and modified PMS were assessed via alkaline phosphatase (ALP) activity, calcium deposition, and osteocalcin and osteopontin mRNA expression. Immobilized Hep-DOPA and BMP-2 on PMS were demonstrated by XPS analysis. BMP-2-immobilized Hep-PMS provided significantly higher ALP activity, calcium deposition, and osteocalcin and osteopontin mRNA expression compared to PMS alone. These results suggest that BMP-2-immobilized Hep-PMS effectively improves MG-63 cell activity. In conclusion, BMP-2-immobilized Hep-PMS can be used to effectively regenerate bone defects. (C) 2015 Elsevier B.V. All rights reserved.
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