TY - JOUR
T1 - Fabrication of hybrid scaffolds by polymer deposition system and its in-vivo evaluation with a rat tibial defect model
AU - Sa, Min Woo
AU - Kim, Sung Eun
AU - Yun, Young Pil
AU - Song, Hae Ryong
AU - Kim, Jong Young
N1 - Publisher Copyright:
© 2014, The Korean Tissue Engineering and Regenerative Medicine Society and Springer Science+Business Media Dordrecht.
PY - 2014/12/10
Y1 - 2014/12/10
N2 - The purpose of this study was to investigate the bone regeneration ability of a polycaprolactone (PCL) tube scaffold fabricated by using a polymer deposition system with G-code and to evaluate the biocompatibility of bone graft material with Bio-C (HA (30%)/TCP (70%)), carboxymethyl cellulose (CMC), and bone morphogenetic protein-2(BMP-2). The fabrication of a rapid prototyping-based PCL tube scaffold requires a combination of several devices, including a heater, pressure dispenser, and motion controller, etc. This system can process polymer with high precision by a 200-μm nozzle. We used scanning electron microscopy to observe the surface of fabricated scaffold. Three groups considered in this study were PCL tube scaffold (Group A), BMP-2(0.1 mg)/Bio-C/CMC/PCL scaffold (Group B), and BMP-2(0.5 mg)/Bio-C/CMC/PCL scaffold (Group C). The functional recovery and bone regeneration potential were estimated by performing an in-vivo animal experiment with a white rat model. Then, the effect of the scaffold on tibial defects in rats was examined by observing an X-ray image at 4 or 8 weeks and by carrying out histological analysis. In this study, scaffolds fabricated by using the PDS (polymer deposition system), had a diameter of 4.0 mm and a height of 8.0 mm. Moreover, we confirmed that group C exhibited better biomedical characteristics for bone formation than the other scaffolds. The evaluation of in-vivo experimental results suggested that the co-fabrication of the PCL tube scaffold with group C resulted in sustained bone regeneration, which in turn improved the biocompatibility of the bone graft material.
AB - The purpose of this study was to investigate the bone regeneration ability of a polycaprolactone (PCL) tube scaffold fabricated by using a polymer deposition system with G-code and to evaluate the biocompatibility of bone graft material with Bio-C (HA (30%)/TCP (70%)), carboxymethyl cellulose (CMC), and bone morphogenetic protein-2(BMP-2). The fabrication of a rapid prototyping-based PCL tube scaffold requires a combination of several devices, including a heater, pressure dispenser, and motion controller, etc. This system can process polymer with high precision by a 200-μm nozzle. We used scanning electron microscopy to observe the surface of fabricated scaffold. Three groups considered in this study were PCL tube scaffold (Group A), BMP-2(0.1 mg)/Bio-C/CMC/PCL scaffold (Group B), and BMP-2(0.5 mg)/Bio-C/CMC/PCL scaffold (Group C). The functional recovery and bone regeneration potential were estimated by performing an in-vivo animal experiment with a white rat model. Then, the effect of the scaffold on tibial defects in rats was examined by observing an X-ray image at 4 or 8 weeks and by carrying out histological analysis. In this study, scaffolds fabricated by using the PDS (polymer deposition system), had a diameter of 4.0 mm and a height of 8.0 mm. Moreover, we confirmed that group C exhibited better biomedical characteristics for bone formation than the other scaffolds. The evaluation of in-vivo experimental results suggested that the co-fabrication of the PCL tube scaffold with group C resulted in sustained bone regeneration, which in turn improved the biocompatibility of the bone graft material.
KW - Bio-C(composite (HA(30%)/β-TCP(70%))
KW - Bone morphogenetic protein-2 (BMP-2)
KW - Carboxymethyl cellulose (CMC)
KW - Polycaprolactone (PCL)
KW - Polymer deposition system (PDS)
KW - Scaffold
UR - http://www.scopus.com/inward/record.url?scp=84916883270&partnerID=8YFLogxK
U2 - 10.1007/s13770-014-0065-0
DO - 10.1007/s13770-014-0065-0
M3 - Article
AN - SCOPUS:84916883270
SN - 1738-2696
VL - 11
SP - 439
EP - 445
JO - Tissue Engineering and Regenerative Medicine
JF - Tissue Engineering and Regenerative Medicine
IS - 6
ER -