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Paper Title Page
Abstract: The purpose of this study was to compare the bone regenerative effect of calcium
phosphate glass according to the particle size in vivo. We prepared two different sizes, that is 400
μm and 40 μm, of calcium phosphate glass powder using the system CaO-CaF2-P2O5-MgO-ZnO.
Critical-sized calvarial defects were created in 60 male Sprague-Dawley rats. The animals were
divided into 3 groups of 20 animals each. Each defect was filled with a constant weight of 0.5 g
calcium phosphate glass powder mixed with saline. As controls, the defect was left empty. The rats
were sacrificed 2 or 8 weeks after postsurgery, and the results were evaluated using histological as
well as histomorphometrical studies. The particle size of the calcium phosphate was crucial; 400
μm particles promoted new bone formation, while 40 μm particles inhibited it because of severe
inflammation.
165
Abstract: The porous apatite-wollastonite bioactive glass-ceramic (AW-GG) was made from
nano-precursor powders derived from sol-gel process, and shaped by dipping method with polymer
foam. The physical-chemical properties, bioactivity and biocompatibility of the materials were
studied by means of TG, XRD, SEM, TEM and so on. The bioactivity was investigated in simulated
body fluid (SBF) and the biocompatibility was evaluated by co-culturing with marrow stromal cells
(MSCs). The result shows that: the particle size of the AW precursor powders is 40~100nm; porous
AW GC has three-dimensional pored structure with 300~500um macropores and 2~5um micropores;
the materials possess high bioactivity and biocompatibility. Porous AW GC may therefore have great
potential application as bone tissue engineering scaffold.
169
Abstract: Factors controlling the antibacterial ability of three bioactive glasses were studied by
comparing the changes in the SBF during immersion of the glasses with their response to four
microorganisms. After immersion of 100 mg/ml fine powder (<45μm) of the glasses in the SBF for
1, 2, 4, 8, 16, 27 and 48 hours, the immersion solutions were filtered and the pH in the bulk solution
was measured. Ionic concentrations of Na, K, Ca, Mg, P and Si ions in the immersion solutions
were determined by ICP-OES. The antibacterial activity of the glasses showed good correlation
with the changes of the pH values in the SBF solutions. No correlation was found between the ionic
concentration and the antibacterial ability of the three glasses against the four tested
microorganisms. The results suggest that, the antimicrobial effect of the glass powder against the
microorganisms tested is mostly dependent on the increase of the pH in the solution to values
detrimental for the bacteria growth.
173
Abstract: CaO-SiO2 gels for bioactive organic-inorganic composites were prepared from
tetraethoxysilane (TEOS) and calcium nitrate tetrahydrate (Ca(NO3)2⋅4H2O) by a sol-gel method
with the addition of the various amount of polyethylene glycol (PEG). The effects of PEG on
morphology and bioactivity of the gel were investigated. The samples with the starting compositions
of Ca(NO3)2 : TEOS = 30 : 70 in molar ratiowere prepared with or without coexistence of PEG. All
the examined gels were obtained as a crack-free bulk bodies after gelation and aging. FT-IR spectra
of the prepared gels showed that the gels have similar contents of silanol groups regardless of the
amount of PEG. SEM observation showed that the gel consists of aggregates of 2-3 μm spherical
particles with a diameter of 2-3 μm when it was prepared with the addition of PEG at a molar ratio of
PEG : TEOS = 0.002 : 1, while it consists of aggregates of spherical particles with a diameter of 50
nm at a molar ratio of PEG : TEOS = 0.004 or 0.007 : 1. The size of the CaO-SiO2 powder can be
decreased with increasing the amount of the added PEG. All the samples, regardless of the amount of
the added PEG, formed apatite on their surfaces in a simulated body fluid (SBF) within 1 d. These
results suggest that bioactive fine spherical particles with various size can be obtained through sol-gel
processing under co-existence of appropriate amounts of PEG.
177
Abstract: fabricated by pressureless sintering process. The effect of BG on the sintering ability and
mechanical strength of the ceramics, and the adhesion and proliferation of osteoblasts were
investigated. The results showed that the optimum amount of BG was 20wt.% and the samples
sintered at 1100oC for 5h revealed a bending strength of 172 MPa, which was approximately
2-times higher than that of the pure CaSiO3 ceramics. The cell experiments showed that BG
reinforced CaSiO3 ceramics supported osteoblast adhesion and possessed higher proliferation than
that of the pure CaSiO3 ceramics, which indicated excellent biocompatibility. Our results suggested
that BG reinforced CaSiO3 ceramics could be potential candidates as bioactive bone implant
materials.
181
Abstract: The aim of this study is to find out the crystallization behaviour and in-vitro bioactivity
character of machinable glass ceramics having different ratios of Na/K mica and apatite phases, to
ascertain the best machinable composition. In order to investigate the bioactivity behavior of the
samples the simulated body fluid (SBF) was prepared. Samples were removed from the solution
after 1 hour, 1 day, 1, 2, 3 and 4 weeks. FEG-SEM was used to characterize the morphology of
precipitation HCA layer on the surface depending on time. Molecular bonding characterization of
HCA layers were carried out by using Fourier Transform Infrared Spectroscopy (FTIR) technique.
The thin film X-ray diffraction (TF-XRD) analysis was used to characterize the variation of
chemical composition on precipitated layer by time. Optimum results were obtained by the
composition, containing 70wt% Na/K mica and 30wt% fluorapatite which had an average mica size
of 3-4 microns.
185
Abstract: Composite biomaterials of calcinated bovine bone derived hydroxyapatite (HA) doped
with 5 and 10 wt% commercial inert glass (CIG) were prepared by sintering. The production of HA
from natural sources satisfies economic and time-saving aims, while the use of CIGs is directed by
economic and ecological aspects. The produced composites were subjected to scanning electron
microscopy (SEM) and X-ray diffraction analysis. Measurements of compression strength,
microhardness, and density were also carried out. The experimental results and their discussion
showed that the type and the composition of incorporated glass are of crucial importance.
Consequently, provided that an optimum amount of glass is incorporated, the resultant materials can
exhibit good values of compression strength and microhardness and hence they can be suggested for
potential use in load-bearing biomedical applications.
189
Abstract: We observed the cytotoxicity of human bone marrow stromal cells(hBMSCs) by microparticles
of bioactive glass with four particle groups(same chemical composition-45S5 but
produced by two different manufacturer and two different size groups). In vivo test using rat
calvaria were also carried out. The apoptosis rates of all small particle groups(10-20 ㎛) were
increased than large(500-700 ㎛ or 200-900 ㎛) particle groups in any culture time and any amount
of particles with statistical significance. In vivo study we observed pathologic signs such as
macrophages and foreign-body giant cells in rat calvaria by micro-particles of bioglass. Small(10-
20 ㎛) sized particles induced foreign body reaction and bone resorption. There was proliferation of
macrophages and cells in large number. But in large particle groups, only fibroblasts were
surrounding the particles. The micro-particles of bioglass induced apoptosis of hBMSC and foreign
body reaction in calvaria of rat, therefore micro-particles of bioglass may cause osteolysis if used in
replacement arthroplasty.
193
Abstract: Nano-sized β-tricalcium phosphate (nano-sized β-TCP) was synthesized by dialysis
process using Ca(NO3)2·4H2O and (NH4)2HPO4 as starting materials. The time needed for the whole
process is much shorter than other reported methods. In this new synthesis, dialysis was used to
remove the unwanted ions, and the removal efficiency of impurity ion was evaluated by comparing
the representative ion NH4
+ between the original slurries and deionized water outside of the dialysis
tube. The resulting powders were characterized by X-ray diffraction (XRD), fourier transform
infrared spectroscopy (FT-IR), and chemical analysis. Results showed the final products are pure
β-TCP. The pictures of high resolution-transmission electron microscope (HR-TEM) further
indicated that β-TCP crystals are around 100nm in diameter.
199
Abstract: The gelation process is of importance for the structure and texture of the silica particle
and further functionalization in the area of biomedical application. In a base-catalysis process the
sodium phosphate or plus calcium nitrate salts could be added to induce the gelling velocity and
particle size distribution. Multivalent anions (phosphate ions) or dication (calcium ions) induce the
microscopic phase separation and accelerate gelation of silica sol. Furthermore, the composite silica
nanospheres show excellent monodispersibility as well as pH-stability in the simulated body fluids
or Tris-HCl buffer solution, which will help to surface modification and functionalization in the
biomolecule-existing environments.
203