Preparation and cytocompatibility of porous zirconia scaffold modified by graphene oxide for bone tissue engineering
10.16571/j.cnki.1008-8199.2019.08.003
- VernacularTitle: 氧化石墨烯修饰三维氧化锆骨组织工程支架的制备及细胞相容性研究
- Author:
Xiao-cui WEI
1
;
Rui MU
1
;
Bo BI
1
;
Bi-yao HAN
1
;
Hong-chuan YU
1
;
Bo CHEN
1
;
Yue WANG
1
;
Xiao-lei SHI
1
;
Sheng-qi ZANG
1
;
Lei JIN
1
Author Information
1. Department of Stomatology, Jinling Hospital, Nanjing School Clinical Medicine, Southern Medical University/General Hospital of Eastern Theater Command, PLA, Nanjing 210002, Jiangsu,China
- Publication Type:Journal Article
- Keywords:
graphene oxide;
Zirconia scaffold;
dental pulp stem cells;
bone tissue engineering
- From:
Journal of Medical Postgraduates
2019;32(8):797-802
- CountryChina
- Language:Chinese
-
Abstract:
Objective In order to meet the needs of maxillofacical bone defect repair, the aim of this study was to synthesize graphene oxide(GO) modified three-dimensional conneted nano- zirconia(ZrO2) bone tissue engineering scaffold and evaluate its surface morphology, compressive strength and cytocompatibility. Methods GO was synthesized by a modified Hummers method and then was testified by scanning electron microscope, transmission electron microscopy and fourier transform infrared spectroscopy. ZrO2 scaffold was modified by different concentrations(0.5,1.0,1.5mg/mL) of GO dispersion via a silane-mediated method. The composite scaffold with uniform GO coating was chosen for compressive strength test and co-cultured with human dental pulp stem cells(hDPSCs). Actin staining was used to observe the growth of the cells on the scaffold, and MTS was used to detect the cell activity. Results The characterization results showed that, under scanning electron microscope, the GO was flaky and the surface morphology of folds could be seen. Part of the GO layer folds up at the edge. Under transmission electron microscopy, the GO was clearly observed to have a gossylike, translucent and slightly wrinkled lamellar structure. The crystal structure in this area in the high-resolution filter image showed a six-member ring structure like graphite. Under high power electron microscope, the 1.0mg/ml GO-ZrO2 scaffold could be seen to deposit a thin layer of GO at the crack of the scaffold skeleton, connecting the two ends of the crack, and lamellar GO with folds could be observed on the surface of ceramic particles. The comparison of mechanical properties showed that the compression strength of GO-ZrO2 scaffold was sgnificantly increased compared with that of ZrO2 scaffold[（1.292±0.087）vs（1.031±0.076）, P<0.05]. Compared with the simple ZrO2 scaffold, the GO-ZrO2 scaffold showed more dense extension and adhesion to the surface of scaffolds, showing more active cell proliferation. The cell viability test showed that the viability of hDPSCs was significantly improved on GO-ZrO2 scaffold after 1, 3 and 5 days of proliferation compared with the simple ZrO2 scaffold(P<0.05). Conclusion The ZrO2 scaffold modified by GO improved compressive strength, promoted the early proliferation of hDPSCs with good cytocompatibility.
