In-situ hybridization of calcium silicate and hydroxyapatite-gelatin nanocomposites enhances physical property and in vitro osteogenesis

被引:9
作者
Chiu, Chi-Kai [1 ]
Lee, Dong Joon [1 ]
Chen, Hsin [2 ]
Chow, Laurence C. [3 ]
Ko, Ching-Chang [1 ,4 ]
机构
[1] Univ N Carolina, Sch Dent, NC Oral Hlth Inst, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Dent, Dept Endodont, Chapel Hill, NC 27599 USA
[3] NIST, Paffenbarger Res Ctr ADAF, Gaithersburg, MD 20899 USA
[4] Univ N Carolina, Sch Dent, Dept Orthodont, Chapel Hill, NC 27599 USA
关键词
BONE; DIFFERENTIATION; PROLIFERATION; SCAFFOLDS; AMINOSILANE; BIOACTIVITY; COMPOSITE; HYBRIDS;
D O I
10.1007/s10856-015-5456-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Low mechanical strengths and inadequate bioactive material-tissue interactions of current synthetic materials limit their clinical applications in bone regeneration. Here, we demonstrate gelatin modified siloxanecalcium silicate (GEMOSIL-CS), a nanocomposite made of gelatinous hydroxyapatite with in situ pozzolanic formation of calcium silicate (CS) interacting among gelatin, silica and Calcium Hydroxide (Ca(OH)(2)). It is shown the formation of CS matrices, which chemically bonds to the gelatinous hydroxyapatite, provided hygroscopic reinforcement mechanism and promoted both in vitro and in vivo osteogenic properties of GEMOSIL-CS. The formation of CS was identified by Fourier transform infrared spectroscopy (FTIR) and powder X-ray diffraction. The interfacial bindings within nanocomposites were studied by FTIR and thermogravimetric analysis. Both gelatin and CS have been found critical to the structure integrity and mechanical strengths (93 MPa in compressive strength and 58.9 MPa in biaxial strength). The GEMOSIL-CS was biocompatible and osteoconductive as result of type I collagen secretion and mineralized nodule formation from MC3T3 osteoblasts. SEM and TEM indicated the secretion of collagen fibers and mineral particles as the evidence of mineralization in the early stage of osteogenic differentiation. In vivo bone formation capability was performed by implanting GEMOSIL-CS into rat calvarial defects for 12 weeks and the result showed comparable new bone formation between GEMOSIL-CS group (20 %) and the control (20.19 %). The major advantage of GEMOSIL-CS composites is in situ self-hardening in ambient or aqueous environment at room temperature providing a simple, fast and cheap method to produce porous scaffolds.
引用
收藏
页数:14
相关论文
共 43 条
  • [1] Osteoinduction, osteoconduction and osseointegration
    Albrektsson, T
    Johansson, C
    [J]. EUROPEAN SPINE JOURNAL, 2001, 10 (Suppl 2) : S96 - S101
  • [2] Baciu D, 2007, J OPTOELECTRON ADV M, V9, P3320
  • [3] Effect of added gelatin on the properties of calcium phosphate cement
    Bigi, A
    Bracci, B
    Panzavolta, S
    [J]. BIOMATERIALS, 2004, 25 (14) : 2893 - 2899
  • [4] Accelerating effects of colloidal nano-silica for beneficial calcium-silicate-hydrate formation in cement
    Björnström, J
    Martinelli, A
    Matic, A
    Börjesson, L
    Panas, I
    [J]. CHEMICAL PHYSICS LETTERS, 2004, 392 (1-3) : 242 - 248
  • [5] Preparation of hydroxyapatite-gelatin nanocomposite
    Chang, MC
    Ko, CC
    Douglas, WH
    [J]. BIOMATERIALS, 2003, 24 (17) : 2853 - 2862
  • [6] Direct scaffolding of biomimetic hydroxyapatite-gelatin nanocomposites using aminosilane cross-linker for bone regeneration
    Chiu, Chi-Kai
    Ferreira, Joao
    Luo, Tzy-Jiun M.
    Geng, Haixia
    Lin, Feng-Chang
    Ko, Ching-Chang
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2012, 23 (09) : 2115 - 2126
  • [7] Bio-inspired calcium silicate-gelatin bone grafts for load-bearing applications
    Ding, Shinn-Jyh
    Wei, Chung-Kai
    Lai, Meng-Heng
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (34) : 12793 - 12802
  • [8] Effect of nanosilica additions on Belite Cement pastes held in sulfate solutions
    Dolado, Jorge S.
    Campillo, Igor
    Erkizia, Edurne
    Ibanez, Jose A.
    Porro, Antonio
    Guerrero, Ana
    Goni, Sara
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2007, 90 (12) : 3973 - 3976
  • [9] Du C, 1999, J BIOMED MATER RES, V44, P407, DOI 10.1002/(SICI)1097-4636(19990315)44:4<407::AID-JBM6>3.0.CO
  • [10] 2-T