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. 2019 Jun 5:24:e00350.
doi: 10.1016/j.btre.2019.e00350. eCollection 2019 Dec.

Enhanced bone regeneration capability of chitosan sponge coated with TiO2 nanoparticles

Affiliations

Enhanced bone regeneration capability of chitosan sponge coated with TiO2 nanoparticles

Radyum Ikono et al. Biotechnol Rep (Amst). .

Erratum in

Abstract

Chitosan has been a popular option for tissue engineering, however exhibits limited function for bone regeneration due to its low mechanical robustness and non-osteogenic inductivity. Here we hybridized chitosan with TiO2 nanoparticles to improve its bone regeneration capability. Morphology and crystallographic analysis showed that TiO2 nanoparticles in anatase-type were distributed evenly on the surface of the chitosan sponges. Degradation test showed a significant effect of TiO2 nanoparticles addition in retaining its integrity. Biomineralization assay using simulated body fluid showed apatite formation in sponges surface as denoted by PO4- band observed in FTIR results. qPCR analysis supported chitosan - TiO2 sponges in bone regeneration capability as indicated by DMP1 and OCN gene upregulation in TiO2 treated group. Finally, cytotoxicity analysis supported the fact that TiO2 nanoparticles added sponges were proved to be biocompatible. Results suggest that chitosan-50% TiO2 nanoparticles sponges could be a potential novel scaffold for bone tissue engineering.

Keywords: Bone regeneration; Chitosan; Sponges; TiO2 nanoparticles; Tissue engineering.

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Figures

Fig. 1
Fig. 1
SEM images of chitosan (chi) - nano TiO2 (NT) sponge of different treatment group: (A) control, (B) chi-12.5%NT, (C) chi-25%NT, and (D) chi-50%NT (E) SEM – EDS image of chi-12.5%NT sponge.
Fig. 2
Fig. 2
XRD analysis of different sample groups. This graph shows that addition of TiO2 to the sponge did not affect the crystal structure of TiO2 shown by anatase crystal structure retention. (NT—X : nano TiO2 – concentration used).
Fig. 3
Fig. 3
Physical appearance (A) and IR spectrum (B) of samples after incubation in SBF solution.
Fig. 4
Fig. 4
DMP1 gene and OCN gene expressions of cells seeded on the scaffold. An asterisk (*) marks represent significant differences between group for DMP1 gene, and an octothorp (#) marks represent significant differences between group for OCN gene (p-value < 0.05).
Fig. 5
Fig. 5
Cell attachment on the scaffold in 40x magnification after staining with crystal violet (Magnification: 1500x).
Fig. 6
Fig. 6
Cytotoxicity analysis using WST assay after 5 days cell culture. Hybridized TiO2 on the chitosan scaffold can significantly improve biocompatibility properties of the scaffold.

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