TY - JOUR
T1 - Rapid-prototyped PLGA/β-TCP/hydroxyapatite nanocomposite scaffolds in a rabbit femoral defect model
AU - Kim, Jinku
AU - McBride, Sean
AU - Tellis, Brandi
AU - Alvarez-Urena, Pedro
AU - Song, Young Hye
AU - Dean, David D.
AU - Sylvia, Victor L.
AU - Elgendy, Hoda
AU - Ong, Joo
AU - Hollinger, Jeffrey O.
PY - 2012/6
Y1 - 2012/6
N2 - Bone tissue engineering scaffolds composed of poly(d,l-lactide:glycolide) (DL-PLGA) and -tricalcium phosphate (-TCP) nanocomposites were prepared and characterized. Scaffolds with two specific architectures were produced via fused deposition modeling (FDM), a type of extrusion freeform fabrication. Microfilaments deposited at angles of 0° and 90° were designated as the simple scaffold architecture, while those deposited at angles alternating between 0°, 90°, 45° and45° were designated as the complex scaffold architecture. In addition, the simple and complex scaffolds were coated with hydroxyapatite (HA). The surface morphology of the scaffolds was assessed before and after HA coating and uniform distribution of HA coating on the surface was observed by scanning electron microscopy. The scaffolds were implanted into rabbit femoral unicortical bone defects according to four treatment groups based on pore structure and HA coating. After 6 and 12 weeks, scaffolds and host bone were recovered and processed for histology. Data suggest that all configurations of the scaffolds integrated with the host bone and were biocompatible and thus may offer an exciting new scaffold platform for delivery of biologicals for bone regeneration.
AB - Bone tissue engineering scaffolds composed of poly(d,l-lactide:glycolide) (DL-PLGA) and -tricalcium phosphate (-TCP) nanocomposites were prepared and characterized. Scaffolds with two specific architectures were produced via fused deposition modeling (FDM), a type of extrusion freeform fabrication. Microfilaments deposited at angles of 0° and 90° were designated as the simple scaffold architecture, while those deposited at angles alternating between 0°, 90°, 45° and45° were designated as the complex scaffold architecture. In addition, the simple and complex scaffolds were coated with hydroxyapatite (HA). The surface morphology of the scaffolds was assessed before and after HA coating and uniform distribution of HA coating on the surface was observed by scanning electron microscopy. The scaffolds were implanted into rabbit femoral unicortical bone defects according to four treatment groups based on pore structure and HA coating. After 6 and 12 weeks, scaffolds and host bone were recovered and processed for histology. Data suggest that all configurations of the scaffolds integrated with the host bone and were biocompatible and thus may offer an exciting new scaffold platform for delivery of biologicals for bone regeneration.
UR - http://www.scopus.com/inward/record.url?scp=84863351526&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84863351526&partnerID=8YFLogxK
U2 - 10.1088/1758-5082/4/2/025003
DO - 10.1088/1758-5082/4/2/025003
M3 - Article
C2 - 22427485
AN - SCOPUS:84863351526
SN - 1758-5082
VL - 4
JO - Biofabrication
JF - Biofabrication
IS - 2
M1 - 025003
ER -