English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 850857      Online Users : 238
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/13216


    Title: 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
    Authors: Chi, CY;Chen, CY;Huang, JY;Kuan, CY;Lin, YY;Li, CH;Yang, CC;Lin, FH
    Contributors: Institute of Biomedical Engineering and Nanomedicine
    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.
    Date: 2021-05-01
    Relation: Ceramics International. 2021 May 1;47(9):2725-12734.
    Link to: http://dx.doi.org/10.1016/j.ceramint.2021.01.132
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0272-8842&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000632837900003
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85099647446
    Appears in Collections:[林峯輝] 期刊論文

    Files in This Item:

    File Description SizeFormat
    SCP85099647446.pdf6825KbAdobe PDF291View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback