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Combined Delivery of Two Different Bioactive Factors Incorporated in Hydroxyapatite Microcarrier for Bone Regeneration

Authors
Kim, Tae-WooAhn, Woo-BeomKim, Joong-MinKim, Joong-HyunKim, Tae-HyunPerez, Roman A.Jang, Hyon-Seok
Issue Date
10월-2020
Publisher
KOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC
Keywords
Drug carriers; BMP-2; VEGF; Drug delivery system; Bone regeneration
Citation
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.17, no.5, pp.607 - 624
Indexed
SCIE
SCOPUS
KCI
Journal Title
TISSUE ENGINEERING AND REGENERATIVE MEDICINE
Volume
17
Number
5
Start Page
607
End Page
624
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/52547
DOI
10.1007/s13770-020-00257-5
ISSN
1738-2696
Abstract
Background: The delivery of growth factors using a carrier system presents a promising and innovative tool in tissue engineering and dentistry today. Two of the foremost bioactive factors, bone morphogenetic protein-2 and vascular endothelial growth factor (VEGF), are widely applied using a ceramic scaffold. The aim of this study was to determine the use of hydroxyapatite microcarrier (MC) for dual delivery of osteogenic and angiogenic factors to accelerate hard tissue regeneration during the regenerative process. Methods: Two MCs of different sizes were fabricated by emulsification of gelatin and alpha-tricalcium phosphate (alpha-TCP). The experimental group was divided based on the combination of MC size and growth factors. For investigating thein vitroproperties, rat mesenchymal stem cells (rMSCs) were harvested from bone marrow of the femur and tibia.For in vivo experiments, MC with/without growth factors was applied into the standardized, 5-mm diameter defects, which were made bilaterally on the parietal bone of the rat. The animals were allowed to heal for 8 weeks, and samples were harvested and analyzed by micro-computed tomography and histology. Results: Improved proliferation of rat mesenchymal stem cells was observed with VEGF loaded MC. For osteogenic differentiation, dual growth factors delivered by MC showed higher osteogenic gene expression, alkaline phosphatse production and calcium deposition. Thein vivoresults revealed statistically significant increase in new bone formation when dual growth factors were delivered by MC. Dual growth factors administered on a calcium phosphate matrix showed significantly enhanced osteogenic potential. Conclusion: We propose this system has potential clinical utility in providing solutions for craniofacial bone defects, with the added benefit of early availability.
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