TY - JOUR
T1 - In vitro and in vivo characterization of multi-walled carbon nanotubes/polycaprolactone composite scaffolds for bone tissue engineering applications
AU - Luo, Feng
AU - Pan, Lanlan
AU - Hong, Guang
AU - Wang, Tong
AU - Pei, Xibo
AU - Wang, Jian
AU - Wan, Qianbing
N1 - Funding Information:
Acknowledgment: The authors acknowledge the financial supports from the Chinese Natural Science Foundation (grant no. 81000659), the Science and Technology Support Program of Sichuan Province (grant nos. 2011FZ0010 and 2016FZ0085), and the State Key Laboratory of Oral Diseases (Sichuan University).
Publisher Copyright:
© 2017 American Scientific Publishers.
PY - 2017/9
Y1 - 2017/9
N2 - For bone regeneration, scaffolds are typically made of degradable and biocompatible materials that provide mechanical support and promote bone formation during the repair and regeneration of damaged bone. Herein, we fabricated multi-walled carbon nanotubes (MWNTs)/polycaprolactone (PCL) composite scaffolds using the solution evaporation technique and characterized their properties in vitro as well as in vivo. The results showed that the added MWNTs were homogeneously distributed throughout the MWNTs/PCL scaffolds. The thermogravimetric analysis (TGA) and in vitro degradation experiments indicated the addition of MWNTs (0.25-2.0 wt%) improved the mechanical and thermal properties of the composite scaffolds, while the PCL grafts still preserved advanced biodegradability. The biomimetic mineralization of the hydroxyapatite (HA) formed on the surface of specimens suggesting that the MWNTs/PCL composite scaffolds had good in vivo bone bioactivity. The scanning electron microscopy images and 3-(4,5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide (MTT) assay results showed that the MWNTs/PCL scaffolds improved the adhesion and proliferation of rat bone-marrow-derived stromal cells (BMSCs) and the scaffolds were supposed to promote osteogenesis. In addition, the in vivo study indicated the MWNTs/PCL scaffolds with 0.5 wt% MWNTs promoted new bone formation with greater bone density and bone regeneration efficacy. Therefore, the MWNTs/PCL scaffolds, with advanced mechanical, biodegradable and biological properties, are suitable candidates for bone tissue engineering applications.
AB - For bone regeneration, scaffolds are typically made of degradable and biocompatible materials that provide mechanical support and promote bone formation during the repair and regeneration of damaged bone. Herein, we fabricated multi-walled carbon nanotubes (MWNTs)/polycaprolactone (PCL) composite scaffolds using the solution evaporation technique and characterized their properties in vitro as well as in vivo. The results showed that the added MWNTs were homogeneously distributed throughout the MWNTs/PCL scaffolds. The thermogravimetric analysis (TGA) and in vitro degradation experiments indicated the addition of MWNTs (0.25-2.0 wt%) improved the mechanical and thermal properties of the composite scaffolds, while the PCL grafts still preserved advanced biodegradability. The biomimetic mineralization of the hydroxyapatite (HA) formed on the surface of specimens suggesting that the MWNTs/PCL composite scaffolds had good in vivo bone bioactivity. The scanning electron microscopy images and 3-(4,5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide (MTT) assay results showed that the MWNTs/PCL scaffolds improved the adhesion and proliferation of rat bone-marrow-derived stromal cells (BMSCs) and the scaffolds were supposed to promote osteogenesis. In addition, the in vivo study indicated the MWNTs/PCL scaffolds with 0.5 wt% MWNTs promoted new bone formation with greater bone density and bone regeneration efficacy. Therefore, the MWNTs/PCL scaffolds, with advanced mechanical, biodegradable and biological properties, are suitable candidates for bone tissue engineering applications.
KW - Biodegradability
KW - Bone tissue engineering
KW - Multi-walled carbon nanotubes (MWNTS)
KW - Polycaprolactone (PCL)
KW - Scaffold
UR - http://www.scopus.com/inward/record.url?scp=85029230161&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85029230161&partnerID=8YFLogxK
U2 - 10.1166/jbt.2017.1629
DO - 10.1166/jbt.2017.1629
M3 - Article
AN - SCOPUS:85029230161
SN - 2157-9083
VL - 7
SP - 787
EP - 797
JO - Journal of Biomaterials and Tissue Engineering
JF - Journal of Biomaterials and Tissue Engineering
IS - 9
ER -