Advanced Materials Research
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Advanced Materials Research
Vols. 47-50
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Advanced Materials Research Vols. 47-50
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Paper Title Page
Surface Morphological Changes Accompanying Dissolution of Bioactive Glass: Effect of Residual Stress
Abstract: We report our observations concerning the time evolution of surface morphology occurring during
the in vitro immersion of bioactive glass surfaces in contact with phosphate buffer solution. We
compare regions under intentionally produced residual stresses via micro-indentation to those where
no indentation was performed. The sign of the residual stress is shown to be important for
predicting dissolution behaviour; compression retards dissolution, whereas tension enhances
dissolution. We analyze our results with a simple model for the work of bond dissociation. We
report that a highly constrained residual compressive stress state, such as in an indent, leads to a
work deficit in comparison to tension, which accounts for the slower dissolution rate of compressed
bioactive glass. Such a mechanochemical effect suggests that the presence of residual stresses from
the manufacture of biomedical implants and devices could lead to accelerated or delayed dissolution
and that careful control of residual stresses should be sought for predictable performance in
dissolvable materials.
1302
Abstract: The effect of pH value at different initial Ca/P molar ratio on the composition and crystal
phase of the calcium phosphates synthesized through chemical precipitation method was studied in
detail. After calcining at 900°C, the products were characterized by XRD and chemical analysis. The
results showed that the composition and crystal phase of the resultant powders can be controlled by
pH value at different initial Ca/P molar ratio. When Ca/P molar ratio was 1.667, pure HA was
obtained at pH values of both 12.0 and 11.0. When initial Ca/P molar ratio was 1.500, pure β-TCP
was obtained at pH value from 11.0 to 9.0. CPP was obtained at pH value from 6.0 to 4.0 when initial
Ca/P molar ratio was 1.000.
1307
Abstract: N-isopropylacrylamide (NIPAM)-ethylene oxide (EO) copolymer was grafted on filter
paper surface to obtain paper-based adsorptive membrane. Protein adsorption on and release from the
membrane was evaluated under various conditions using humanized monoclonal antibody as model
protein. The results obtained indicated that amphiphilic copolymer modified filter paper could be
used as a novel chromatographic membrane for protein separation/purification. Comb-block
copolymers of NIPAM with N-vinylpyrrolidone (VP) were prepared through RAFT polymerization
and macromonomer techniques. Surface modification of substrates, such as plastics and glass, was
carried out by treatment of the substrates in aqueous solution of the amphiphilic comb-block
copolymer (adsorptive coating, pre-adsorption). It was found that the adsorbed copolymer layer was
stable in aqueous environment even when shear stress was applied. Protein adhesion on the material
surfaces before and after the modification was investigated using lysozyme as model protein. The
results obtained showed that the adsorptive coating layer on the material surfaces significantly
reduced non-specific protein adhesion.
1311
Abstract: The near-infrared (NIR) sensitive Au-Au2S nanoparticles (NPs) have shown many advantages as
potential drug delivery systems. To further investigate biological safety of Au-Au2S NPs,
cytotoxicity was estimated by calcein AM/EthD-1 fluorescence staining and the lactate
dehydrogenase (LDH) release. The effects of NPs on apoptosis of CHL cells were determined by
flow cytometry with Annexin V-FITC/PI double staining. It is evident that the Au-Au2S NPs are
non-cytotoxic below IC50 dosage.
1315
Abstract: Novel hybrid biomaterial of gelatin-siloxane nanoparticles (GS NPs), with positive
surface potential and lower cytotoxicity, was synthesized through a 2-step sol-gel process. The
pDNA-GS NPs complex was formulated with high encapsulation efficiency, and exhibited and
efficient transfection in vitro. We thus envision that the GS NPs material could serve as non-viral
gene vectors for gene therapy.
1319
Abstract: Photonic crystals have wide applications not only in optoelectronic fields but also in
bioassays. In this review, we summarized our work on colloidal photonic crystals as novel
biomolecular supports in multiplex bioassays. Except for enhancing the fluorescence signal and
encoding the biomolecular carriers in fluorphore labeled bioassays, photonic crystal can also encode
suspended arrays. From the point view of practicality, the synthesis and self-assembly of
monodispersed colloidal spheres for colloidal crystals is involved.
1323
Abstract: Biodegradable nanofiber has become a popular candidate as tissue engineering scaffolds due to its
biomimic structure as natural extracellular matrix (ECM). Certain tissue regeneration may require
prolonged in vitro culture time for cellular reorganization and tissue remodeling. Therefore, long
term understanding of cellular effects on scaffold degradation is needed. Although there are some
degradation studies on nanofiber, degradation study of nanofibers with cell culture is rare. In our
study, polyglycolide (PGA), poly(DL-lactide-co-glycolide) (PLGA), poly(L-lactide-co-ε-
caprolactone) [P(LLA-CL)] were electrospun into nanofiber scaffolds. The scaffolds were cultured
with porcine smooth muscle cells (PSMC) for up to 3 months to evaluate their degradation behavior
and cellular response. The results showed that their degradation rates were in the order of
PGA>>PLGA>P(LLA-CL). PGA nanofiber degraded in 3 weeks and only supported cell growth in
the first few days. Cell culture accelerated the surface erosion of PLGA and P(LLA-CL) nanofiber
while the bulk degradation remained unaffected. Furthermore, the cell culture did not significantly
reduce the mechanical strength of PLGA and P(LLA-CL) during degradation.
1327
Abstract: This paper reported a newly designed retrievable urethral stent used in treatment of
urethral strictures. The spiral urethral stent is made of Poly (l-lactide) (PLLA), adding barium
sulphate (BaSO4) to certain content, which can be displayed precisely under X-ray after implanted in
body. The stent was clinically tested in 32 patients with recurrent urethral strictures and was left in the
urethra for 5 to 12 months. The response to the effect of the stent was assessed using symptom scores,
peak flow rate (Qmax), residual urine volume (RUV), stent degradation, infection and outcome.
During the treatment, there were not any inflammations found. The mechanical properties of the stent
are almost the same as those of the PLLA stent without BaSO4. Improvements in patient symptom
score, mean Qmax and RUV were significant at the 18 month follow-up. The infection was not
observed. The stent was taken out easily through urethral forceps. In no patient was the stent
obstructed by incrustation for up to 1.5 years.
1331
Abstract: Materials used to make artificial vessels and hearts can cause thrombosis, thus hindering
the development of these therapeutic aids. Endothelial cells (ECs) play a key role in thrombosis, so
in this study, we used human umbilical vein endothelial cells (HUVEC) and tested the
hemocompatibility of different biomaterials. We then measured the signal proteins MAPK
(mitogen-activated protein kinase) and Nuclear Factor- kB (NF-κB) to investigate the correlation
between their expression and the degree of hemocompatibility. The results showed that ECs in the
polyurethane (PU-60) group had significantly more NF-κB than the negative control (p<0.5). To
identify whether the increased expression of NF-κB was induced by MAPK activation, we
investigated changes in phosphorylated MAPK. We found both MAPK and NF-κB are ideal
indicators for evaluating the hemocompatibility of biomaterial.
1335
Abstract: The aim of this study was to evaluate the suitability of CaF2 doping tricalcium silicate
(Ca3SiO5, C3S) as dental restorative materials. The solid state reaction method was used to prepare
CaF2 doping C3S (F-C3S) using CaCO3, SiO2 and CaF2 as the starting materials. The in vitro
bioactivity, the rate of heat evolution and the compressive strength were investigated. The in vitro
bioactivity was examined by soaking the pastes in simulated body fluid (SBF). The FTIR and SEM
results indicated the hydroxycarbonate apatite (HCA) layers of F-C3S pastes and pure C3S pastes
occurred after soaking for 1 day and 3 days, respectively. The difference in bioactivity was
attributed to the formation of F-substituted apatite, which has a Ksp lower than HCA. As compared
with the pure C3S, the rate of heat evolution during the hydration of F-C3S was slower. This was
avail to the dimensional stability of dental restorative materials. The pastes of F-C3S had a lower
early compressive strength in the early stage, but a higher compressive strength in the later stage.
Our results indicated that F-C3S would be bonded better to the teeth because of the earlier formation
of HCA and the higher later compressive strength. F-C3S may be a progressive candidate for dental
restorative materials.
1339