Preparation of chitosan‐nanohydroxyapatite composite scaffolds by a supercritical CO2 assisted process

In this study, chitosan‐nanohydroxyapatite composite scaffolds were prepared by a supercritical fluid assisted process. For this purpose, different amounts of nanohydroxyapatite particles, that is, 0.25, 0.50, and 1.00 wt% were added to chitosan (deacetylation degree: DD 75–85%) solution (2%, w/v, in acetic acid). The gels were then frozen at −20°C, treated in acetone and dried in a supercritical fluid extractor under a constant CO₂ flow of 15 g/min at 35°C and 200 bar for 5 h to obtain porous scaffolds. Scanning electron microscope views showed that the drying of gels under supercritical CO₂ lead to the formation of microporous scaffolds with a pore size distribution of 30–150 μm. Addition of nanohydroxyapatite particles did not significantly affect the pore size distribution. Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy and X‐Ray diffraction analyses supported the successful incorporation of nanohydroxyapatite particles in the scaffold. An increase in water uptake and mechanical strength were observed in composite scaffolds. The results obtained from this study indicated that chitosan‐nanohydroxyapatite scaffolds prepared by using supercritical CO₂ shall be considered as a potential candidate for bone tissue engineering applications. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Improvement of mechanical properties and in vitro bioactivity of freeze-dried gelatin/chitosan scaffolds by functionalized carbon nanotubes

Functionalized multiwall carbon nanotubes (f-MWCNTs) were used to reinforce the freeze-dried gelatin (G)/chitosan (Ch) scaffolds for bone graft substitution. Two types of G/Ch scaffolds at a ratio of 2:1 and 3:1 by weight incorporated with 0.025, 0.05, or 0.1 and 0.2 or 0.4?wt% f-MWCNT, respectively, were prepared by freeze drying, and their structure, morphology, and physicochemical and compressive mechanical properties were evaluated. The scaffolds exhibited porous structure with pore size of 80–300 and 120–140?µm for the reinforced scaffolds of G/Ch 2:1 and 3:1, respectively, and porosity 90–93% which slightly decreased with an increase in f-MWCNTs content for both types. Incorporation of f-MWCNTs led to 11- and 9.6-fold increase in modulus, with respect to their pure biopolymer blend scaffolds at a level of 0.05?wt% for G/Ch 2:1 and 0.2?wt% for G/Ch 3:1, respectively. The higher content of f-MWCNTs resulted in loss of mechanical properties due to agglomeration. The highest value of compressive strength and modulus was obtained for G/Ch 2:1 with 0.05?wt% f-MWCNT as 411?kPa and 18.7?MPa, respectively. Improvement of in vitro bioactivity as a result of f-MWCNTs incorporation was proved by formation of a bone-like apatite layer on the surface of scaffolds upon immersion in simulated body fluid. The findings indicate that the f-MWCNT-reinforced gelatin/chitosan scaffolds may be a suitable candidate for bone tissue engineering.     

Preparation and antibacterial activity of C2-benzaldehyde-C6-aniline double Schiff base derivatives of chitosan

C₂-benzaldehyde-C₆-aniline double Schiff base derivatives of chitosan were synthesized with positioning protection method for the first time. The structures and properties of the new synthesized products were characterized by Fourier transform infrared spectroscopy, ¹³C nuclear magnetic resonance, scanning electron microscope image, X-ray diffraction, and elemental analysis. The elemental analysis results indicated that the degrees of substitution of the products were from 39.6% to 48.2%. The synthesized compounds exhibited an excellent solubility in organic solvents. The antibacterial activities of all of the derivatives were tested in the experiment, and the results showed that the prepared chitosan derivatives had significantly improved antibacterial activity of chitosan and C₂-benzaldehyde Schiff bases of chitosan toward Staphylococcus aureus (ATCC 25923) and Escherichia coli (ATCC 35218). Antibacterial activity of the Schiff bases against E. coli differs from the substituent at the same position of different anilines and increases as the sequence aniline?>?p-toluidine?>?o-toluidine, and the antibacterial activity of the Schiff bases against S. aureus increases as the sequence p-toluidine?>?aniline?>?o-toluidine. The I_C50 of the C₂-benzaldehyde-C₆-aniline double Schiff base derivatives of chitosan against E. coli and S. aureus is 0.0035 and 0.0031?mg?L^?1, respectively, much lower than that of chitosan (0.0064?mg?L^?1) and C₂-benzaldehyde Schiff bases of chitosan (0.0054?mg?L^?1). The cytotoxicity test showed that compared with chitosan and C₂-benzaldehyde Schiff bases of chitosan, the prepared chitosan derivatives had lower cytotoxicity against SCG-7901. This paper provided a new method for the synthesis of Schiff bases of chitosan, which was enlightening.     

Microwave-assisted synthesis and characterization of antibacterial O-crosslinked chitosan hydrogels doped with TiO2 nanoparticles for skin regeneration

Abstract

Tissue engineering provides alternative solutions to traditional transplantation. In this study a novel strategy of chitosan scaffolds obtainment based on selective O-crosslinking using Aspartic acid and the addition of TiO₂ nanoparticles is presented. Prepared under microwave conditions biomaterials were of increased mechanical and thermal durability thanks to NPs presence comparing to pure chitosan. Moreover porous scaffolds maintained antimicrobial activity against S. Aureus and E. Coli. Biomaterials were susceptible to in vitro biodegradation and degradation. Hydrogels exhibited positive impact on proliferation activity of fibroblasts. Thus they may be applied as 3D scaffolds in tissue engineering focused on wound healing.     

Novel Fe2O3-doped glass /chitosan scaffolds for bone tissue replacement

In this study quaternary bioglass system (BG) SiO₂–CaO–Na₂O–P₂O₅ doped with Fe₂O₃ was prepared by the sol–gel method. Furthermore, 3D scaffolds were designed through blending Fe₂O₃ -doped bioglass with chitosan to obtain various compositions of scaffolds by the freeze-drying technique. The thermal behavior, morphological properties, porosity (%), mechanical properties and physicochemical properties of BG and scaffolds were evaluated by DSC/TGA, TEM, SEM, liquid displacement method, universal testing machine, XRD and FTIR. In addition, the in vitro bioactivity of the prepared scaffolds was studied in phosphate buffer saline (PBS) through the determination of PBS ions concentrations, as well as the degradation and the observation of precipitated calcium phosphate layer by SEM coupled with EDX and FTIR behavior. The cell viability of the prepared scaffolds was conducted against Baby Hamster Kidney fibroblasts (BHK-21) cell line. The presence of Fe₂O₃ decreased the T_g (from 513 to 390?°C) and the size decreased (from 20.89 to 50.81–13.92–27.87?nm). The scaffolds porosity (%) decreased upon Fe₂O₃ doping but the mechanical strength increased. Cell viability results for the designed scaffolds demonstrated acceptable cell viability compared with normal cells. Therefore, the designed scaffolds are promoted as regenerated materials that can be used for bone tissue replacement.     

Effects of Acylation and Crosslinking on the Material Properties and Cadmium Ion Adsorption Capacity of Porous Chitosan Beads

Abstract

Chitosan is a novel glucosamine biopolymer derived from the shells of marine organisms. This biopolymer is very attractive for heavy metal ion separations from wastewater because it is selective for toxic transition metal ions over less toxic alkali or alkane earth metal ions. Highly porous, 3-mm chitosan beads were prepared by an aqueous phase-inversion technique for casting gel beads followed by freeze drying. In the attempt to simultaneously improve material properties and adsorption capacity, chitosan was chemically modified by 1) homogeneous acylation of amine groups with nonanoyl chloride before bead casting, and 2) heterogeneous crosslinking of linear chitosan chains with the bifunctional reagent glutaric dialdehyde (GA) after bead casting but before freeze drying. The random addition of C₈ hydrocarbon side chains to about 7% of the amine groups on uncrosslinked chitosan beads via N-acylation improved the saturation adsorption capacity from 169 to 216 mg Cd²⁺/g-bead at saturation (pH 6.5, 25°C) but only slightly reduced solubility in acid solution. Crosslinking of the N-acylated chitosan beads with 0.125 to 2.5 wt% GA in the crosslinking bath increased the internal surface area from 40 to 224 m²/g and rendered the beads insoluble in 1 M acetic acid (pH 2.36). However, crosslinking of the N-acylated chitosan beads reduced the saturation adsorption capacity to 136 mg Cd²⁺/g-bead at 0.75 wt% GA and 86 mg Cd²⁺/g-bead at 2.5 wt% GA. Crosslinking also significantly reduced the compression strength. There was no clear relationship between internal surface area and adsorption capacity, suggesting that the adsorbed cadmium was not uniformly loaded into the bead.     

Mechanical modeling of silk fibroin/TiO2 and silk fibroin/fluoridated TiO2 nanocomposite scaffolds for bone tissue engineering

Biocompatible and biodegradable three-dimensional scaffolds are commonly porous which serve to provide suitable microenvironments for mechanical supporting and optimal cell growth. Silk fibroin (SF) is a natural and biomedical polymer with appropriate and improvable mechanical properties. Making a composite with a bioceramicas reinforcement is a general strategy to prepare a scaffold for hard tissue engineering applications. In the present study, SF was separately combined with titanium dioxide (TiO₂) and fluoridated titanium dioxide nanoparticles (TiO₂-F) as bioceramic reinforcements for bone tissue engineering purposes. At the first step, SF was extracted from Bombyx mori cocoons. Then, TiO₂ nanoparticles were fluoridated by hydrofluoric acid. Afterward, SF/TiO₂ and SF/TiO₂-F nanocomposite scaffolds were prepared by freeze-drying method to obtain a porous microstructure. Both SF/TiO₂ and SF/TiO₂-F scaffolds contained 0, 5, 10, 15 and 20 wt% nanoparticles. To evaluate the efficacy of nanoparticles addition on the mechanical properties of the prepared scaffolds, their compressive properties were assayed. Likewise, the pores morphology and microstructure of the scaffolds were investigated using scanning electron microscopy. In addition, the porosity and density of the scaffolds were measured according to the Archimedes’ principle. Afterward, compressive modulus and microstructure of the prepared scaffolds were evaluated and modeled by Gibson–Ashby’s mechanical models. The results revealed that the compressive modulus predicted by the mechanical model exactly corresponds to the experimental one. The modeling approved the honeycomb structure of the prepared scaffolds which possess interconnected pores.

     

Formation and leachability of hexavalent chromium in the Al2O3-CaO-MgO-Cr2O3 system

The Al₂O₃-CaO-MgO-Cr₂O₃ system has immense potential for refractory castables applications. However, Cr(III) can potentially be oxidized to carcinogenic Cr(VI) during the usage, which can cause subsequent problems with disposal. Equilibrium experiments on the Al₂O₃-CaO-MgO-4wt%Cr₂O₃ system were performed at 1500?°C in air. The effect of MgO addition (0 and 20?wt%) on the formation and leachability of hexavalent chromium was investigated using XPS, XRD, SEM-EDS, the TRGS 613 standard Cr(VI) leaching test and multiple leaching tests. A Cr(VI)-containing phase Ca₄Al₆CrO₁₆ predominantly formed in the samples with 0 and 5?wt% MgO, while the Cr(III)-containing Mg(Al, Cr)₂O₄ spinel phase formed in the samples with 10 and 20?wt% MgO. Addition of MgO suppressed the formation of Cr(VI) while favored the formation of spinel phase. Concentrations of Cr(VI) in the leachates from TRGS 613 tests exceeded the European limit of 0.0002?wt% in all samples, although decreased significantly with 20?wt% MgO addition.     

Preparation and characterization of porous scaffold composite films by blending chitosan and gelatin solutions for skin tissue engineering

Biodegradable polymers have significant potential in biotechnology and bioengineering. However, for some applications, they are limited by their inferior mechanical properties and unsatisfactory compatibility with cells and tissues. In the present investigation blends of chitosan and gelatin with various compositions were produced as candidate materials for biomedical applications. Fourier transform infrared spectral analysis showed good compatibility between these two biodegradable polymers. The composite films showed improved tensile properties, highly porous structure, antimicrobial activities, low water dissolution, low water uptake and high buffer uptake compared to pure chitosan or gelatin films. These enhanced properties could be explained by the introduction of free ? OH, ? NH₂ and ? NHOCOCH₃ groups of the amorphous chitosan in the blends and a network structure through electrostatic interactions between the ammonium ions (? NH³⁺) of the chitosan and the carboxylate ions (? COO^?) of the gelatin. Scanning electron microscopy images of the blend composite films showed homogeneous and smooth surfaces which indicate good miscibility between gelatin and chitosan. The leafy morphologies of the scaffolds indicate a large and homogeneous porous structure, which would cause increased ion diffusion into the gel that could lead to an increase in stability in aqueous solution, buffer and temperature compared to the gelatin/chitosan system. In vivo testing was done in a Wistar rat (Rattus norvegicus) model and the healing efficiencies of the scaffolds containing various compositions of chitosan were measured. The healing efficiencies in Wistar rat of composites with gelatin to chitosan ratios of 10:3 and 10:4 were compared with that of a commercially available scaffold (Eco‐plast). It was observed that, after 5 days of application, the scaffold with a gelatin to chitosan ratio of 10:3 showed 100% healing in the Wistar rat; however, the commercial Eco‐plast showed only a little above 40% healing of the dissected rat wound. Copyright © 2012 Society of Chemical Industry     

Hot corrosion resistance of air plasma sprayed ceramic Sm2SrAl2O7 (SSA) thermal barrier coatings in simulated gas turbine environments

Samarium strontium aluminate (Sm₂SrAl₂O₇-SSA) and Yttria-stabilized zirconia (YSZ) thermal barrier coatings (TBCs) were developed on NiCrAlY bond coated Inconel 718 superalloy substrate using air plasma spray process. The hot corrosion study was conducted in simulated gas turbine environments (molten mixtures of 50?wt% Na₂SO₄ + 50?wt% V₂O₅ and 90?wt% Na₂SO₄ + 5?wt% V₂O₅ + 5?wt% NaCl) for two different temperatures of 700 and 900?°C. A developed SSA TBCs showed about 8% and 22% lower lifetime at 700 and 900?°C, respectively than YSZ TBCs in 50?wt% Na₂SO₄ +?50?wt% V₂O₅ (vanadate). The hot corrosion life of SSA TBCs being found about 13% and 39% lower than YSZ TBCs in 90?wt% Na₂SO₄ +?5?wt% V₂O₅ +?5?wt% NaCl (chloride) at 700 and 900?°C, respectively. X-ray diffraction results showed the formation of SmVO₄, SrV₂O₆, and SrSO₄ as a major hot corrosion product in 50?wt% Na₂SO₄ +?50?wt% V₂O₅ and 90?wt% Na₂SO₄ +?5?wt% V₂O₅ +?5?wt% NaCl environments respectively for SSA TBCs. Similarly, YSZ TBCs also showed YVO₄ as hot corrosion product in vanadate and chloride environments. Both the TBCs suffer a more severe hot corrosion attack in chloride environment at 900?°C. The leaching of Sr²⁺ and Y³⁺ ions from SSA and YSZ respectively play a vital role in the destabilization of coating in vanadate and chloride environments at 700 and 900?°C. In both SSA and YSZ TBCs, the leaching of ion has significantly low influence as compared to attack by chloride ions at the bond coat-top coat interface in the presence of chloride environment. The hot corrosion resistance of SSA TBCs was improved three times higher in the presence of MgO and NiO inhibitor in vanadate environment at 900?°C mainly due to the formation of a stable Ni₃V₂O₈ phase at the surface.     

Effect of ZrO2 content on the mechanical properties and microstructure of HAp/ZrO2 nanocomposites

This paper presents the effect of Zirconia (ZrO₂ =?0, 5, 10, 15, 20 and 25?wt%) on the mechanical properties and micro structural studies of Hydroxyapatite (Ca₁₀(PO₄)₆(OH)₂) (HAp) nano composites. HAp and Zirconia nano composites of 20–40?nm were produced using High Energy Ball milling at 300?rpm for 1?h. X-ray diffraction studies showed that the crystallite and grain size gradually decreased with the increase in ZrO₂ content till 20?wt%, after which there was a sudden raise in both parameters. A dominant ZrO₂ phase was observed in X-ray diffraction studies of sintered samples. Mechanical properties were found to significantly improve on adding 20?wt% of ZrO₂ at 1200?°C. However, the addition of 25?wt% of ZrO₂ powder decreased the mechanical properties of HAp. The reduction could be due to the increase in grain size and dominant smaller particles of ZrO₂. The improved mechanical properties were correlated with the observed micro structural features.     

The effect of TiO2 additive on sinterability and properties of SiC-Al2O3-Y2O3 composite system

In the current research, the effects of TiO₂ additive on mechanical and physical properties of SiC bodies, sintered by liquid phase methods were investigated. Al₂O₃ and Y₂O₃ were used as sintering-aids (10?wt% in total) with an Al₂O₃/Y₂O₃ ratio of 43/57 to provide liquid phase during Sintering. TiO₂ was also used as the oxide additive with an amount ranging from 0 to 10?wt%. After scaling and mixing the starting materials by a planetary mill, the obtained slurry was dried at 100?℃ for four hours. The derived powders were finally pressed under a pressure of 90?MPa. The samples were then pyrolyzed and sintered at 600?℃ and 1900?℃, respectively under argon atmosphere for 1.5?h. Phase analysis showed no trace of TiO₂ after the sintering process, demonstrating the complete TiO₂ to TiC transformation. The results showed that an increase in TiO₂ content up to 5?wt%, led an improvement in all the measured properties including the relative density, hardness, Young's modulus, bending strength, indentation fracture resistance and the brittleness factor, reaching to 96.2%, 24.4?GPa, 395.8?GPa, 521?MPa, 5.8?MPa?m^1/2 and 286.5?×?10^?6 m^?1, respectively. However more than 5?wt% additive resulted in a decrease in all the above-mentioned properties. Microstructural studies demonstrated that crack deflection and crack bridging were the major mechanisms responsible for an increase in the indentation fracture resistance.     

Mechanical and structural properties of polylactide/chitosan scaffolds reinforced with nano-calcium phosphate

In this study, chitosan/polylactide scaffolds reinforced with nano-calcium phosphate (average crystallite size of 16.5?nm) (CP) were fabricated to create a material with excellent properties for bone tissue engineering applications via freeze-casting method. The structural and mechanical properties of nanocomposite scaffolds were studied by increasing amount of chitosan/poly lactide ratio and nano-CP content in both dry and hydrate states, which reflected the exact status of scaffolds in a real biomechanical environment. The morphologies of the nanocomposite scaffolds were viewed using scanning electron microscopy (SEM) and all the scaffolds exhibited a high porosity (up to 92?%) with open pores of 38?C387???m average diameters, which decreased with increased chitosan/polylactide ratio and nano-CP content. Also, SEM photograph of the cross-sectional area of the scaffold showed nano-CP was dispersed all over the polymer matrix thoroughly. The results of mechanical tests showed that the compressive modulus (E) and compressive stress (??) enhanced, when chitosan and nano-CP increased. X-ray diffraction analysis indicated typical chitosan, polylactic acid and nano-CP peaks and showed that the increase in nano-CP weight percentage increased its peak intensities. In addition, the effect of pore-size distributions of the scaffolds with the same composition was studied in relation to mechanical properties. The results showed substantial differences in the pore-size distributions of scaffolds with the same composition prepared, which have no effect on their dry states.     

Preparation of elastic chitosan/poly(<Emphasis Type="SmallCaps">l</Emphasis>-lactide-co-ε-caprolactone) macroporous scaffolds by acetylation and particulate leaching

For soft tissue engineering applications, 3-D macroporous acetylated chitosan/poly(l-lactideco-ε-caprolactone) (PLCL) scaffolds were prepared by acetylation and particulate leaching using sodium acetate in an acidic water/dioxane solution. Acetylated 5 wt% chitosan/PLCL scaffold of 90% porosity was determined and confirmed through various tests. The physiochemical properties of acetylated chitosan/PLCL hybrid scaffolds were examined by measuring water contact angles, pore morphology and interconnectivity using scanning electron microscopy (SEM), and dye release testing. In addition, mechanical properties such as tensile strength and bending stress recovery for determining the elasticity of scaffolds were measured. The fibroblast cell line NIH-3T3 was used to test relative cell affinities for the acetylated chitosan/PLCL vs. normal chitosan/PLCL films and porous scaffolds. The acetylated chitosan/PLCL films and scaffolds showed a high initial cell adhesion after 4 h of cell culture and increased cell proliferation compared to that of the control. The acetylated chitosan/PLCL scaffolds produced by particulate leaching showed a highly porous structure and improved the biocompatibility and stability of chitosan compared to that of chitosan-coated PLCL scaffolds. Thus, these scaffolds may be very useful for a variety of tissue engineering applications.     

Fabrication and characterization of Li4SiO4-Li2TiO3 composite ceramic pebbles using extrusion and spherodization technique

The effect of different amount of Li₂TiO₃(LT) (0–15?wt%) addition on the properties of composite Li₄SiO₄ (LS) ceramic pebbles were studied. The Li₄SiO₄-Li₂TiO₃ composite powder was prepared in-situ using solid state method at a calcination temperature as low as 800?°C. The composite pebbles were fabricated using a cost-effective and simple technique called extrusion-spherodization. The sintered pebbles were characterized for density, grain size, pore size distribution, crush load and moisture stability. The density of Li₄SiO₄ composite pebbles was improved for LS-5?wt% LT in comparison to LS pebbles when fired at 1000?°C. Moreover, the LS grain size in the composite pebbles was reduced (5.8?μm) in comparison to LS pebbles. We also found that the average crush load value of the LS-5?wt%LT composite pebbles had been improved by nearly 100% (33?N) to that of the pure LS pebbles (17?N). The LS-5?wt% LT pebbles showed improvement in stability to moisture.     

Spark plasma sintering and mechanical properties of compounds in TiB2-SiC pseudo-diagram

The influence of spark plasma sintering (SPS) parameters (temperature, time, pressure) and the role of particle size on densification, microstructure and mechanical properties of commercial additive-free TiB₂, SiC and composites thereof were studied by X-ray diffraction, scanning electron microscopy, the ultrasonic method and indentation. Three particle sizes of SiC and 2 of TiB₂ were processed. An optimal cycle was found for TiB₂ and SiC: 2000?°C, 3?min dwell time, and 100?MPa applied at 600?°C. The relative density of pure SiC increases linearly from 70% to 90% when the initial particle size decreases from 1.75?µm to 0.5?µm. Pure TiB₂ was densified up to 87%. Using 2.5?wt% SiC in TiB₂, the relative density increases to 97%. Young's modulus and the hardness of all samples were measured, with results discussed. The higher properties were obtained for additive-free TiB₂–5%SiC with a relative density of 97% and with the Young's modulus and Vickers hardness values being close to 378?GPa and 23?GPa, respectively.     

Toughening of aromatic diamine-cured epoxy resins by modification with hybrid modifiers composed of N-phenylmaleimide–styrene copolymers and N-phenylmaleimide–styrene–p-hydroxystyrene terpolymers

Hybrid modifiers composed of N-phenylmaleimide–styrene copolymers (PMS), and N-phenylmaleimide–styrene–p-hydroxystyrene terpolymers (PMSH) containing pendent p-hydroxyphenyl groups as functionalities, were used to improve the toughness of bisphenol-A diglycidyl ether epoxy resin cured with p,p′-diaminodiphenyl sulphone. The hybrid modifiers were effective in toughening the epoxy resin. When using the modifier composed of 10 wt% PMS (M?_w 313000) and 2.5 wt% PMSH (2.5 mol% p-hydroxystyrene units, M?_w 316000), the fracture toughness (K_IC) for the modified resins increased 100% with no deterioration in the flexural properties and the glass transition temperature. The improvement in toughness of the epoxy resins was attained because of the co-continuous phase structure and the improvement in interfacial adhesion. The toughening mechanism is discussed in terms of the morphological characteristics of the modified epoxy resin systems.     

Microstructure,phase compositions and in vitro evaluation of freeze casting hydroxyapatite-silica scaffolds

Hydroxyapatite-silica (HA-SiO₂) scaffolds with different SiO₂ content (0, 2, 5 and 10 wt% SiO₂) were fabricated by freeze casting. After sintering, the scaffolds maintained the interconnected unidirectional pore channels by removing the frozen ice crystals via sublimation. X-ray diffraction (XRD) analysis indicated that SiO₂ promoted the decomposition of HA to tricalcium phosphate (TCP), comprised of α-TCP and β-TCP, which became more apparent with the increase of SiO₂ content. The microstructure observation of scanning electron microscope (SEM) showed that the scaffolds surface feature had great changes in terms of grain size and grain boundary with the addition of SiO₂. Moreover, the addition of SiO₂ could increase the porosity and pore size of the scaffolds, even allowing it to reach a maximum as the SiO₂ content increased to 5 wt%. Compression tests investigated the variation in the compressive strength of the scaffolds with the increase in the SiO₂ content, which showed first decreasing and then increasing behavior. In vitro evaluation results in simulated body fluid (1.5×SBF) revealed that the introduction of SiO₂ enhanced the growth rate of bone-like layer, especially the scaffold with 5 wt% SiO₂, which exhibited faster growth rate of bone-like layer than the other scaffolds. The XRD and fourier transformed infrared spectroscopy (FT-IR) characterization confirmed that the bone-like layer formed on the scaffold surface was a carbonate-containing hydroxyapatite bone-like layer.     

Silver Loaded Nanofibrous Curdlan Mat for Diabetic Wound Healing: An In Vitro and In Vivo Study

A fibrous scaffold of curdlan/poly(vinyl alcohol) (PVA) blend is prepared by electrospinning technique and antimicrobial property is imparted to it by the addition of silver nitrate (1, 3, and 5 wt%). All the scaffolds except the PVA/curdlan with 5 wt% AgNO₃ show good viability of Swiss 3T3 fibroblast cells. Significant reductions in the growth of Staphylococcus aureus and Escherichia coli are also observed in all the scaffolds. In vitro scratch assay and cell adhesion studies indicate that the scaffold containing 1% AgNO₃ shows significant wound healing and better cell spreading. The in vivo results also show faster healing of excision wounds in diabetic rats treated with the same material when compared to the control and the commercial sample. Furthermore, downregulation of proinflammatory cytokines and upregulation of anti‐inflammatory cytokines on the skin of the treated animals confirm that PVA/curdlan/1% AgNO₃ electrospun mat could be a promising material for diabetic wound healing.     

Calcium/chitosan spheres as catalyst for biodiesel production

Chitosan, an abundant biopolymer extracted from crustacean shells, can be used as a structuring agent by the insertion of calcium oxide and used as a catalyst in transesterification reactions. These calcium‐incorporated chitosan spheres were calcined in order to obtain a porous calcium catalyst without organic material. The materials were characterized using X‐ray diffraction, thermogravimetric analysis, Fourier transform infrared and X‐ray photoelectron spectroscopies, temperature‐programmed desorption of CO₂, scanning electron microscopy and specific surface area analysis. Afterwards the calcined calcium/chitosan spheres were used in the transesterification reaction of sunflower oil with methanol. The conversion of sunflower oil to methyl esters (Y_FAME), under optimized reaction conditions, which were determined by factorial experimental design (X_MR, 1:9; X_CAT, 3 wt%; time, 4 h; temperature, 60 °C; magnetic stirring, 1000 rpm), was 56.12 ± 0.32 wt%. These results show that chitosan can be used as a precursor for the formation of calcium/chitosan spheres, yielding a porous calcium oxide (with higher surface area) that can be used as an alkaline catalyst for biodiesel production. © 2014 Society of Chemical Industry