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This study was to evaluate the acid-buffering capacity and antibacterial properties of orthodontic adhesives containing bioactive glasses (BAGs) (45S5, 45S5F, S53P4), Hydroxyapatite, beta-tricalcium phosphate, and Canasite. Fillers comprising 15 wt% bioactive glasses, HAp, β-TCP, and Canasite incorporated with 55 wt% silanated glass were added to a mixture of UDMA/TEGDMA. Acid-buffering capacity was tested by exposing disc-shaped samples of each adhesive to medium of bacteria-produced acids, and pH changes were recorded at 24 and 48 h. Antibacterial properties were assessed by indirect testing by exposing polymerized adhesive samples to a medium and direct testing by immersing the specimens in solutions containing S. mutans and S. sanguinis. A significant buffering capacity was shown by the 45S5, 45S5F and S53P4 BAG adhesives. The antibacterial properties were not significant in all experimental adhesives. Therefore, the experimental orthodontic adhesives containing BAGs demonstrated a significant buffering capacity but did not show significant antibacterial properties against S. mutans and S. sanguinis.

The aim was to assess the effect of powder to liquid ratio (PLR) on setting time, fluoride release, and compressive strength of conventional glass ionomer cements (GICs) containing pre-reacted spherical glass fillers (SPG). GICs were prepared by mixing SPG with Fuji IX Universal liquid using PLR of 1:1, 1.5:1, 2:1, 2.5:1, 3:1. Setting time decreased from 221 to 51 s upon rising PLR. Increasing PLR decreased cumulative fluoride release (33 to 13 ppm). Diffusion coefficient of fluoride of experimental GICs (1.6-1.8×10-8 cm2/s) was comparable with that of Fuji IX Universal (1.6×10-8 cm2/s). Compressive strength of PLR 2:1 to 3:1 (93-140 MPa) were comparable with that of Fuji IX Universal (124 MPa). These results demonstrated that rising powder ratio reduced setting time, fluoride release, and compressive strength of GICs. However, the setting time and strength experimental GICs with PLR greater than 2:1 were in the acceptable range of the ISO standard.

The aim of this study was to prepare RMGICs for pulp protection that contain polyacids functionalized with methacrylate groups (CMs) to enable light-activated polymerization without the need for toxic 2-hydroxyethyl methacrylate (HEMA) monomers. The effects of using CM liquids with 0 or 5 wt% HEMA on the physical/mechanical properties and cytotoxicity of the experimental RMGICs were assessed. Spherical pre-reacted glass fillers (SPG) were used as the powder phase. The experimental RMGICs were prepared by mixing SPG with CM liquid (0 wt% HEMA, F1) or CMH liquid (5 wt% HEMA, F2). Commercial materials (Vitrebond, VB, TheraCal LC, TC) were used for the comparisons. The degree of monomer conversion and fluoride release of both F1 and F2 were significantly lower than those of VB. F1 showed comparable biaxial flexural strength with VB but higher strength than TC. The dimensional stability (mass/volume changes) of the experimental materials was comparable with that of the commercial materials. F1 and F2 exhibited higher Sr/Ca ion release and relative cell viability than VB. The use of CMH liquid reduced the strength but enhanced the fluoride release of the experimental RMGICs. In conclusion, the experimental RMGICs showed comparable strength but lower cytotoxicity compared to the commercial RMGICs. These novel materials could be used as alternative materials for pulp protection.

The objective of this study was to evaluate the antibacterial properties and pH changes of bioactive glasses and zinc oxide nanowire in different concentrations. Bioactive glasses (45S5 and 45S5F) were prepared in three concentrations of 10, 20, and 50 mg/ml and zinc oxide nanowire was prepared in 1 and 5 mg/ml concentrations. The materials were exposed to 500 ml brain heart infusion broth (BHI) with 1.5 x 107 of S.mutans and S.sanguinis separately. Antibacterial properties were tested indirectly by collecting 100 ml of each sample and transferred into a 96 well-plate. The optical density (OD) was evaluated using spectrophotometry at 630 nm at 24h and 48h. The pH changes were recorded. The data were statistically analyzed by Kruskal-Wallis tests. The result showed that the pH changes were significantly different in the Bioactive glass samples, while zinc oxide nanowire showed stable pH. Antibacterial activity against S.mutans was significant lower for 45S5 at 50 mg/ml, 45S5F and zinc oxide nanowire in all concentrations at 24 h. While in 48 h, 45S5, 45S5F and zinc oxide nanowire showed significant antibacterial activity in all concentration except 45S5F at 10 mg/ml. Antibacterial activity against S.sanguinis was significant for 45S5 and 45S5F at 20 and 50 mg/ml and zinc oxide nanowire in all concentration at 48h. It can be concluded that Bioactive glasses (45S5 and 45S5F) exhibited antibacterial properties and pH changes depending on its concentration, while zinc oxide nanowire exhibited antibacterial properties at low concentrations with a constant pH value.

The aim of this study was to assess the effect of different commercial liquid phases (Ketac, Riva, and Fuji IX) and the use of spherical pre-reacted glass (SPG) fillers on cement maturation, fluoride release, compressive (CS) and biaxial flexural strength (BFS) of experimental glass ionomer cements (GICs). The experimental GICs (Ketac_M, Riva_M, FujiIX_M) were prepared by mixing SPG fillers with commercial liquid phases using the powder to liquid mass ratio of 2.5:1. FTIR-ATR was used to assess the maturation of GICs. Diffusion coefficient of fluoride (DF) and cumulative fluoride release (CF) in deionized water was determined using the fluoride ion specific electrode (n=3). CS and BFS at 24 h were also tested (n=6). Commercial GICs were used as comparisons. Riva and Riva_M exhibited rapid polyacrylate salt formation. The highest DF and CF were observed with Riva_M (1.65x10-9 cm2/s) and Riva (77 ppm) respectively. Using SPG fillers enhanced DF of GICs on average from ~2.5x10-9 cm2/s to ~3.0x10-9 cm2/s but reduced CF of the materials on average from ~51 ppm to ~42 ppm. The CS and BFS of Ketac_M (144 and 22 MPa) and Fuji IX_M (123 and 30 MPa) were comparable to commercial materials. Using SPG with Riva significantly reduced CS and BFS from 123 MPa to 55 MPa and 42 MPa to 28 MPa respectively. The use of SPG fillers enhanced DF but reduced CF of GICs. Using SPG with Ketac or Fuji IX liquids provided comparable strength to the commercial materials. Resumo O objetivo deste estudo foi avaliar o efeito de diferentes fases líquidas comerciais (Ketac, Riva e Fuji IX) e o uso de partículas esféricas de vidro pré-reagido (SPG) na maturação do cimento, liberação de flúor, força de compressão (CS) e resistência biaxial à flexão (BFS) de cimentos de ionômero de vidro (GICs) experimentais. Os GICs experimentais (Ketac_M, Riva_M, FujiIX_M) foram preparados pela mistura de partículas SPG com fases líquidas comerciais usando a proporção de pó para massa líquida de 2,5: 1. O FTIR-ATR foi usado para avaliar a maturação dos GICs. O coeficiente de difusão do flúor (DF) e a liberação cumulativa de flúor (CF) em água deionizada foram determinados usando o eletrodo específico do íon fluoreto (n = 3). CS e BFS em 24 h também foram testados (n = 6). GICs comerciais foram usados como comparações. Riva e Riva_M exibiram rápida formação de sal de poliacrilato. Os maiores DF e CF foram observados com Riva_M (1,65x10-9 cm2/s) e Riva (77 ppm), respectivamente. O uso de partículas SPG melhorou o DF de GICs em média de ~ 2,5x10-9 cm2/s a ~ 3,0x10-9 cm2/s, mas reduziu o CF dos materiais em média de ~ 51 ppm a ~ 42 ppm. O CS e BFS de Ketac_M (144 e 22 MPa) e Fuji IX_M (123 e 30 MPa) foram comparáveis aos materiais comerciais. Usar SPG com Riva reduziu significativamente CS e BFS de 123 MPa para 55 MPa e 42 MPa para 28 MPa, respectivamente. O uso de SPG partículas melhorou o DF, mas reduziu o CF dos GICs. O uso de partículas SPG com líquidos Ketac ou Fuji IX proporcionou resistência comparável aos materiais comerciais.

BACKGROUND Polycaprolactone (PCL)-biphasic calcium phosphate (BCP) scaffolds fabricated using Melt-Stretching and Compression Molding (MSCM) can release calcium and phosphate ions, which are essential for bone formation. OBJECTIVE Responses of the osteoblasts seeded on three groups of scaffolds including group A; PCL-20% BCP (%wt), group B; PCL-30% BCP and group C (control); pure PCL (100% PCL) were evaluated. METHODS The cell-scaffold constructs were made by seeding osteoblast cell lines at 1×105 cells/scaffold. The constructs of each group were divided for culturing in proliferation medium (PR) and osteogenic induction medium (OS) for 30 days. RESULTS The cells attached and grew on the scaffolds of all groups. The cell number and the differentiation markers of groups A and B were remarkably higher than those of group C over the observation periods. Slow proliferation of the cells of group A and B in the PR medium in the first 7 days corresponded to the maximum increases in alkaline phosphatase activities (ALP). The maximum levels of ALP of those groups in the OS medium were not detected until day 14. The levels of osteocalcin of those groups were not statistically different when cultured in both mediums. CONCLUSIONS The MSCM scaffolds are suitable for supporting attachment and growth of the osteoblasts. Additional BCP into the PCL-based scaffolds accelerate early differentiation of the cells in the constructs even without osteogenic-inductive condition.

Background Biocompatibility and degradation of poly e-caprolactone (PCL)-Biphasic Calcium Phosphate (BCP) scaffolds fabricated by the "Melt Stretching and Compression Molding (MSCM)" technique were evaluated in rat models. Objectives Degradation behaviors and histological biocompatibility of the PCL-20% BCP MSCM scaffolds and compare with those of PCL-20% β-tricalcium phosphate (TCP) scaffolds commercially fabricated by Fused Deposition Modeling (FDM) were evaluated. Methods The study groups included Group A: PCL-20% BCP MSCM scaffolds and Group B: PCL-20% TCP FDM scaffolds, which were implanted subcutaneously in twelve male Wistar rats. On day 14, 30, 60 and 90, dimensional changes of the scaffolds and their surrounding histological features were assessed using Micro-Computed Tomography (μ-CT) and histological analysis. Changes of their molecular weight were assessed using Gel Permeation Chromatography (GPC). Results Formation of collagen and new blood vessels throughout the scaffolds of both groups increased with time with low degrees of inflammation. The μ-CT and GPC analysis demonstrated that the scaffolds of both groups degraded with time, but, their molecular weight slightly changed over the observation periods. All results of both groups were not significantly different. Conclusions The PCL-20% BCP MSCM scaffolds were biocompatible and biodegradable in vivo. Their properties were comparable to those of the commercial PCL-20% TCP scaffolds.

A composite of 70/30 poly(lactic acid)/hydroxyapatite was systematically prepared using various amounts of glycidyl methacrylate as reactive compatibilizer or Joncryl ADR®-4368 containing nine glycidyl methacrylate functions as a chain extension/branching agent to improve the mechanical and biological properties for suitable usage as internal bone fixation devices. The effect of glycidyl methacrylate/Joncryl on mechanical properties of poly(lactic acid)/hydroxyapatite was investigated through flexural strength. Cell proliferation and differentiation of osteoblast-like MC3T3-E1 cells cultured on the composite samples were determined by Alamar Blue assay and alkaline phosphatase expression, respectively. Result shows that flexural strength tends to decrease, as glycidyl methacrylate content increases except for 1 wt.% glycidyl methacrylate. With an addition of dicumyl peroxide, the flexural strength shows an improvement than that of without dicumyl peroxide probably due to the chemical bonding of the hydroxyapatite and poly(lactic acid) as revealed by FTIR and NMR, whereas the composite with 5 wt.% Joncryl shows the best result, as the flexural strength increases getting close to pure poly(lactic acid). The significant morphology change could be seen in composite with Joncryl where the uniform agglomeration of hydroxyapatite particles oriented in poly(lactic acid) matrix. Addition of the epoxy functional compatibilizers at suitable percentages could also have benefits to cellular attachment, proliferation, differentiation and mineralization. So that, this poly(lactic acid)/hydroxyapatite composite could be a promising material to be used as internal bone fixation devices such as screws, pins and plates.

Calcium phosphate cements (CPCs) have been extensively used as bone graft substitutes for the repair of bone defect due to its biocompatibility, osteoconductivity and in-situ setting capability. They poorly degrade thus limiting their use in tissue engineering application. A possible strategy to improve the speed of CPC degradation is to add porogen to CPC to create macropores that can enhance cement resorption and can consequently be replaced by new bone. The as-generated macropores are generally not connected because of spherical shape of the porogens which can limit the extent of newly formed bone. The aim of this study was to fabricate CPCs having tubular macroporous structure by incorporating fast-dissolving maltodextrin microstrips (MDMS) and explore their properties such as setting time, mechanical property, microstructure and degradability of the cements. The results showed that after immersing MDMS-embedded composites in simulated body fluid under physiological condition for 1 d MDMS rapidly disintegrated (more than 70%), generating tubular macropores in CPCs. The disintegration of MDMS completed in 1 week. CPCs containing MDMS lower than 30% by weight had the same final setting time as those without MDMS. The average values of compressive strength of the CPC composites decreased with the disintegration of MDMS. % Porosity and pore interconnectivity increased with increasing MDMS content. In addition, MDMS-embedded CPCs were cell friendly with excellent cell adhesion, indicating a possible candidate as bone graft substitutes.

The production of the biomimetic scaffolds with well-designed porosity parameters is a critical and challenging factor in biomaterials processing. The porosity parameters (i.e., pore size, pore shape, and distribution pattern) impact scaffold permeability, proteins/cells infiltration, and angiogenesis. This study introduced a new approach for the production of gradient porous nanocomposite scaffolds with controllable porosity and permeability using basic biomaterials of collagen and nanobiphasic calcium phosphate (nBCP) powder consisting of nano HA/β-TCP. A modified freeze-drying method (i.e., variables; collagen/nBCP ratio and quenching rates) was integrated for the first time with the chemical foaming method with the use of vitamin E as a potential surfactant and porogen. Vitamin E successfully increased the range of pore size, pore interconnection, and scaffold permeability. Further control of collagen/nBCP ratios and quenching rates allowed modulation of the pore morphology, total porosity, and the surface roughness of the scaffold. Scaffolds produced using vitamin E with collagen/nBCP ratio of 92/8% at -80°C quenching rate displayed a multimodal heterogeneous pore network with a wide range of pore sizes of mostly round/oval and polygonal pore morphology. Furthermore, these scaffolds revealed a more consistent gradient porous network with peripheral large pores-that gradually become smaller toward scaffold central-that produced a significantly higher permeability and better support of initial cellular performances. Accordingly, considering the various potentials of vitamin E, this study would provide promising insight into the production of smart and customized scaffolds for regenerative and therapeutic applications.

The aim of this study was to prepare experimental resin-modified glass ionomer cements (RMGICs) containing low levels of hydroxyethyl methacrylate (HEMA) for pulp protection. Liquid and powder phases of the experimental RMGICs were polyacid functionalized with methacrylate groups and spherical pre-reacted glass fillers (SPG). Two types of liquid phase containing 0 wt. % HEMA (CM liquid) or 5 wt. % HEMA (CMH liquid) were formulated. The experimental RMGICs were prepared by mixing SPG fillers with CM liquid (F1) or CMH liquid (F2). Rheological properties were examined using a strain-controlled rheometer (n = 5). The Vickers microhardness (n = 5) and dentin shear bond strength (SBS) (n = 10) of the materials were tested. Commercial pulp protection materials (Vitrebond and TheraCal LC) were used as comparisons. The viscosity and surface microhardness of F1 (22 m Pa·s, 18 VHN) and F2 (18 m Pa·s, 16 VHN) were significantly higher than those of Vitrebond (6 mPa·s, 6 VHN) and TheraCal (0.1 mPa·s, 7 VHN). The SBS of F1 (10.7 MPa) and F2 (11.9 MPa) was comparable to that of Vitrebond (15.4 MPa) but higher than that of TheraCal LC (5.6 MPa). The addition of 5 wt. % HEMA showed no significant effect on viscosity, surface microhardness, or SBS of the experimental RMGICs. The experimental materials showed higher viscosity and microhardness but similar SBS when compared with the commercial RMGIC.

Physical properties and biocompatibility of polycaprolactone (PCL)–biphasic calcium phosphate (BCP) scaffolds fabricated by the modified melt stretching and multilayer deposition (mMSMD) technique were evaluated in vitro. The PCL–BCP scaffold specimens included group A; PCL: BCP (wt%) = 80:20 and group B; 70:30. Mechanical properties of the scaffolds were assessed using a universal testing machine. Degradation behaviors of the scaffolds were assessed over 60 days. The amount of calcium and phosphate ions released from the scaffolds was detected over 30 days. Attachment and growth of osteoblasts on the scaffolds and indirect cytocompatibility to those cells were evaluated. The results showed that the scaffolds of both groups could withstand compressive forces on their superior aspect very well; however, their lateral aspect could only withstand light forces. Degradation of the scaffolds over 2 months was low (group A = 1.92 ± 0.47% and group B = 2.9 ± 1.3%, p > 0.05). The concentrations of calcium and phosphate ions released from the scaffolds of both groups significantly increased on day 7 ( p

A series of TiO2 modified hydroxyapatite composites (HA/TiO2) with different compositions were prepared. Phase formations and morphologies of the obtained HA/TiO2 composite were characterised using X-ray diffraction and SEM, and their photocatalytic activities were also determined by decomposition of methylene blue solution. Filter cloths were prepared by depositing the composite on polyester non-wovens via pad dry cure, and their filtering effectiveness was examined by photocatalytic activity measurement and bactericidal test. Hydroxyapatite/TiO2 composites were successfully prepared and exhibited photocatalytic properties. With increasing ratio of anatase titania in the HA/TiO2 composite from 20 to 30 and 50%, photocatalytic activity of composite material increased such that HATi5050 composite exhibited the highest photocatalytic activity. Non-woven filters coated with HA/TiO2 composites also exhibited good photocatalytic activities. Less difference in photocatalytic activity between HATi7030 an...

To improve biphasic calcium phosphate (BCP) ceramic strength, well known biocompatible and strong ceramics such as SiO2, ZrO2 and TiO2 were added to BCP with hydroxyapatite/tricalcium phosphate ratios of 70:30 (BCP7030). SiO2, ZrO2 and TiO2 powders with 2, 5 and 10 wt-% each were mixed with the BCP7030 powder. X-ray diffractometry and scanning electron microscopy (SEM) were used to determine the crystal structures and morphology of the sintered samples respectively. The physical properties and flexural strength of the samples were measured. Cell proliferation and differentiation of osteoblast-like Saos-2 cells cultured on BCP ceramics were determined by Alamar Blue assay and alkaline phosphatase expression respectively. Finally, SEM was performed to investigate the cell morphology on the surfaces of the specimens. The BCP7030 sample with 10 wt-%TiO2 displayed an optimum bending strength of ∼61 MPa and showed the strongest enhancement of cell proliferation and differentiation among all tested reinf...

This study aims to improve the strength of porous BCP samples by the addition of titanium dioxide (TiO2), the well known biocompatible and strong ceramic. BCP powder with HA/TCP ratio of 70/30 (BCP7030) obtained by mixing a pure HA and β-TCP powder. TiO2 powder with 2 (BCP_2Ti), 5 (BCP_5Ti) and 10 (BCP_10Ti) %wt were added into the BCP7030 powder, then ball milled in ethanol for 6 hrs. The porous samples were fabricated by the combination of the gel-casting and freeze drying techniques. All samples were sintered at 1100°C for 2 hrs. X-ray diffractometry (XRD) and scanning electron microscopy (SEM) were used to determine crystal structures and morphology of the sintered samples, respectively. Mechanical properties and porosity of samples were measured by using the universal testing machine and Archimedess principle, respectively. XRD results showed that the phases of the undoped sample can be indexed HA and β-TCP with the ratio of 70/30 as the major phases. In BCP_2Ti, CaTiO3 was observed as a minor phase among the crystallization of HA and β-TCP with the proportion of 30:70. Meanwhile, in BCP_5Ti and BCP_10Ti, XRD patterns revealed a completely transformation of HA to β-TCP with minor phases of CaTiO3 and TiO2. The microstructure of sintered samples present highly porous structure which consisted of two-dimensional pore channels along the long axis and the short axis, which replicates the ice and pore orientation in the direction of freezing. Relatively, the porosity of the samples was increased with the amount of TiO2. Surprisingly, an additions of the TiO2 was not rather improved the mechanical strength of porous BCP7030 in this study. This might be a result of a high percentage of porosity (84%).

Purpose: This study aimed to evaluate the effect of biphasic calcium phosphate (BCP) with high hydroxyapatite/tricalcium phosphate (HA/TCP) ratios on bone formation in rabbit calvarial defects. Materials and Methods: Sixteen New Zealand white rabbits were randomly divided into two groups, a control group and an experimental group. In each animal, bilateral circular defects (10-mm diameter) were created on the calvarium. In the control group (three rabbits per time frame), defects were grafted with autogenous bone chips in one side and left empty in the other side. In the experimental group (five rabbits per time frame), defects were grafted with BCP1 (HA:TCP, 8:2) in one side and BCP2 (HA:TCP, 9:1) in the contralateral side. The animals were sacrificed at 2 and 8 weeks as designated. Bone formation and residual grafting material were assessed by radiographic densitometry, microcomputed tomography (micro-CT), and histomorphometric analysis. Results: Histologic observation revealed that BCP1, BCP2, and the autogenous bone group preserved good contours of the defect, while the unfilled defect group showed connective tissue healing. Micro-CT analysis at 8 weeks showed the comparable percentages of bone volume fraction (% BV/TV) of BCP1 (20.70% ± 2.76%) and BCP2 (20.72% ± 3.97%) and two times higher than that of 2 weeks (9.90% ± 0.75%, 10.57% ± 0.85%). The autogenous group had a significantly (P < .005) greater % BV/TV (34.58% ± 8.85%) than other groups. The percentage of the material volume fraction of BCP1 and BCP2 was not different. The histomorphometry demonstrated a higher increase in newly formed bone from 2 to 8 weeks in all groups, and all were comparable (autogenous: 4.30% ± 0.76%, 12.83% ± 7.74%; unfilled: 2.82% ± 1.19%, 8.14% ± 6.35%; BCP1: 3.01% ± 2.57%, 8.81% ± 3.86%; BCP2: 3.24% ± 1.09%, 10.27% ± 3.98%). Conclusion: BCP with a high ratio of HA presented good osteoconductive properties and space-maintaining capacity and would be beneficial for long-term preservation or when stable graft volume is essential.

The biphasic calcium phosphate (BCP) concept was introduced to overcome disadvantages of single phase biomaterials. In this study, we prepared BCP from nanoHA and β-TCP that were synthesized via a solid state reaction. Three different ratios of pure BCP and collagen-based BCP scaffolds (%HA/%β-TCP; 30/70, 40/60 and 50/50) were produced using a polymeric sponge method. Physical and mechanical properties of all materials and scaffolds were investigated. XRD pattern proved the purity of each HA, β-TCP and BCP. SEM showed overall distribution of macropores (80-200 µm) with appropriate interconnected porosities. Total porosity of pure BCP (93% ± 2) was found to be higher than collagen-based BCP (85%± 3). It was observed that dimensional shrinkage of larger scaffold (39% ± 4) is lower than smaller one (42% ± 5) and scaffolds with higher HA (50%) ratio experienced greater shrinkage than those with higher β-TCP (70%) ratio (45% ±3 and 36% ±1 respectively). Mechanical properties of both groups tend to be very low and collagen coating had no influence on mechanical behavior. Further studies may improve the physical properties of these composite BCP.

The aim of this study is to investigate glass compositions containing BaO and MgO with a view to improve the mechanical properties of conventional glass ionomer cements. Two glass systems based on the compositions of SiO2–Al2O3–CaF2–TiO2 and SiO2–Al2O3–CaF2–ZrO2 were prepared and reacted with an in-house produced co-poly(alkenoic acid) to produce glass ionomer cements. X-ray diffraction and X-ray fluorescence were used to determine the phases and chemical compositions of the glass after melting. The morphologies of the glass powder and cement surfaces were analysed by SEM. The compressive strength and the working and setting times of the cements were also measured. Cements prepared from glass systems of SiO2–Al2O3–CaF2–TiO2 and SiO2–Al2O3–CaF2–ZrO2 containing barium and magnesium ions showed significantly increased strength compared to their original glasses. ZrBa1Mg1 cement that contained equal amounts of barium/magnesium oxide possessed high cement strength at ∼110 MPa but long setting time at ∼16 min. ...

Honeycomb structures of TiO2-modified hydroxyapatite composite (HA/TiO2) were fabricated using extrusion technique. The mixture formulations of HA/TiO2 extrusion pastes (S1-S4) were investigated to optimize the process. The filtering effectiveness of the HA/TiO2 honeycombs was evaluated by photocatalytic activity measurement and a bactericidal test. The effects of sintering temperature and honeycomb thickness on photocatalytic and antibacterial activities were additionally studied. The S3 and S4 honeycomb samples, sintered at 650°C, exhibited a similar trend in reducing methylene blue concentration. At 800°C, the S3 honeycomb sample showed a slightly faster reduction in methylene blue concentration compared to the S4 honeycomb. Honeycomb samples of 2 and 5 cm in thickness showed significantly greater photocatalytic activity than that of 1 cm such that methylene blue concentrations rapidly decreased after UV exposure for 24 hours. The S3 and S4 honeycomb samples also exhibited decomposition of both gram-negative E. coli and gram-positive S. aureus. Approximately 50% of gram-positive S. aureus and gramnegative E. coli were decomposed by the honeycombs in the sample-thickness dependent manner after 2 hours of UV exposure. Low survival ratios of bacteria (5% - 10%) were observed after 6 hours of UV exposure and the 2 mm and 5 mm thick honeycomb samples showed the greatest and most similar antibacterial activities.

The biphasic calcium phosphate (BCP) concept was introduced to overcome disadvantages of single phase biomaterials. Different composition ratios of BCP bioceramics have been studied, yet controversies regarding the effects of ratio on biomaterial behavior still exist. In this study, BCP scaffolds were prepared from nano hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) that were synthesized via a solid state reaction. Three different composition ratios of pure BCP and collagen-based BCP scaffolds (%HA/%β-TCP; 30/70, 40/60, and 50/50) were produced using a polymeric sponge method. Physical and mechanical properties of all materials and scaffolds were investigated. SEM showed overall distribution of both macropores (80–200 μm) and micropores (0.5–2 μm) with high interconnected porosities. Total porosity of pure BCP (90% ± 3%) was found to be higher than collagen-based BCP (85% ± 2%). It was observed that following sintering process, dimensional shrinkage of large scaffolds (39% ± 4%) was lower than small ones (42% ± 5%) and scaffolds with high HA ratios (50%) experienced higher dimensional changes than those with higher β-TCP (70%) ratios (45% ± 3% and 36% ± 1%, respectively). Compressive strength of both groups was less than 0.1 MPa and collagen coating had almost no influence on mechanical behavior. Further studies may improve the physical properties of these scaffolds and investigate their exact biological behaviors. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A: 2260–2268, 2012.