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  4. Preparation and in-vitro evaluation of Fe2O3-doped DP-bioglass in combination with 3D-printing and selective laser sintering process (3DP-SLS) for alveolar bone augmentation
 
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Preparation and in-vitro evaluation of Fe2O3-doped DP-bioglass in combination with 3D-printing and selective laser sintering process (3DP-SLS) for alveolar bone augmentation

Journal
Ceramics International
Journal Volume
47
Journal Issue
9
Pages
12725-12734
Date Issued
2021
Author(s)
Chi C.-Y
Chen C.-Y
Huang J.-Y
Kuan C.-Y
Lin Y.-Y
Li C.-H
Yang C.-C
Lin F.-H.
Lin, Feng-Huei  
DOI
10.1016/j.ceramint.2021.01.132
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85099647446&doi=10.1016%2fj.ceramint.2021.01.132&partnerID=40&md5=3f9ed43178c2b0edb9eb545a5316ff6a
https://scholars.lib.ntu.edu.tw/handle/123456789/577128
Abstract
Severe periodontal disease can cause damage and atrophy of alveolar bone. Presently, Fe2O3-doped DP-bioglass (DPF-bioglass) was prepared and combined with a 3D-printing and selective laser sintering (3DP-SLS) process to prepare a porous scaffold for alveolar bone augmentation of dental implants. Addition of 2% Fe2O3 effectively lowered the melting point and darkened the color to absorb the laser energy and increased the sintering efficiency. X-ray diffraction, optical microscopy (OM), energy dispersive spectrophotometry, and differential thermal analysis were used to characterize the crystal structure, color/darkness, morphology, qualitative chemical composition, and thermal stability, respectively, for the synthesized DPF-bioglass. After the human fetal osteoblasts (hFOB 1.19 cells) were cultured with the extraction medium, cell morphology was observed by OM. The WST-1 and lactate dehydrogenase (LDH) assays were used to evaluate the cytotoxicity of the DPF-bioglass. This bioglass was then prepared as an alveolar bone substitute (ABS) by the 3DP-SLS process and cells were cultured on the scaffold. The cell morphology was revealed by scanning electron microscopy (SEM). Cell survival rate and cells in early apoptosis were examined using live/dead and JC-1 staining, respectively. The gene expression of Runx2, type I collagen, and alkaline phosphatase (ALP) were analyzed by qPCR to check early osteogenesis, extracellular matrix secretion, and mineralization, respectively. Xylenol orange (XO) staining was used to observe the mineralization of calcium phosphate deposition. The improvements in cell attachment, proliferation, and biomineralization were further confirmed in terms of potential bone regeneration in vitro. The developed ABS was not cytotoxic to human osteoblasts in the WST-1, LDH, live/dead and JC-1 stain. The developed ABS gradually degraded and constantly released Ca+2, PO4?3, Fe+3, and Si+4 in the physiological environment. SEM and XO staining revealed that the released ions promoted bone formation and mineralization. Osteogenesis was also enhanced, as judged by early induction of the gene expression. ? 2021 Elsevier Ltd and Techna Group S.r.l.
Subjects
Alkalinity; Biomineralization; Bone; Calcium phosphate; Cell death; Chemical stability; Crystal structure; Differential thermal analysis; Gene expression; Hematite; Laser heating; Mineralogy; Morphology; Phosphatases; Polymerase chain reaction; Scaffolds (biology); Scanning electron microscopy; Silicon implants; Sintering; Tissue regeneration; ALkaline phosphatase; Calcium phosphate deposition; Chemical compositions; Extracellular matrices; In-vitro evaluation; Lactate dehydrogenase assays; Periodontal disease; Physiological environment; Selective laser sintering
SDGs

[SDGs]SDG3

[SDGs]SDG7

Other Subjects
Alkalinity; Biomineralization; Bone; Calcium phosphate; Cell death; Chemical stability; Crystal structure; Differential thermal analysis; Gene expression; Hematite; Laser heating; Mineralogy; Morphology; Phosphatases; Polymerase chain reaction; Scaffolds
Type
journal article

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