Design, synthesis, photophysical and electrochemical properties of 2-(4,5-diphenyl-1-p-aryl-1H-imidazol-2-yl)phenol-based boron complexes.

New hybrid organic-inorganic boron compounds using an imidazole core have been readily synthesized by a two-step procedure from commercially available simple starting materials. All boron compounds were fully characterized by multinuclear NMR spectroscopy, LC-MS, thermogravimetric analysis, cyclic voltammetry and single crystal X-ray diffraction analysis (for & ). The photoluminescence measurements of revealed distinct emission peak maxima located at 378, 379 and 387 nm, respectively. Electroluminescent devices fabricated using these boron compounds () suggest that the boron compounds are capable of transporting electrons. A maximum brightness of 6450 cd m(-2) at 12.5 V was realized when compound was used as an electron-transporting material.

Evenly distributed thin-film Ag coating on stainless plate by tricomponent Ag/silicate/PU with antimicrobial and biocompatible properties.

A tricomponent nanohybrid dispersion in water comprising silver nanoparticles (AgNP), nanometer-thick silicate platelets (NSP), and water-based polyurethane (PU) was developed for surface coating on orthopedic metal plates. The previously developed AgNP-on-NSP nanohybrid was homogeneously blended into a selected waterborne PU dispersion at varied weight ratios from 1/0.1 to 1/10 (w/w). PU was used to adhere the Ag nanohybrid to the metal surface. The resultant dispersions were analyzed and found to contain AgNP 2-18 nm in diameter and characterized by using UV absorption and TEM micrograph. The subsequent coating of AgNP/NSP-PU dispersion generated a film of 1.5 µm thickness on the metal plate surface, further characterized by an energy dispersive spectroscope (EDS) to show the homogeneous distribution of Ag, Si, and C elements on the metal plates. The surface antimicrobial efficacy was proven for the coating composition of AgNP/NSP to PU ranging from 1/1 to 1/5 by weight ratio but irrelevant to the thickness of the coated materials. The metal plate coated with the high Ag content at 1/1 (w/w) ratio was shown to have very low cytotoxicity toward the contacted mammal fibroblasts. Overall, the optimized tricomponent Ag/silicate/PU in water dispersion from 1/2 to 1/3 (w/w) could generate a stable film on a metal surface exhibiting both antimicrobial and biocompatible properties. The facile coating technique of the AgNP/NSP in waterborne PU is proven to be viable for fabricating infection- and cytotoxicity-free medical devices.

In vitro and in vivo evaluation of chitosan-gelatin scaffolds for cartilage tissue engineering.

Chitosan-gelatin polyelectrolyte complexes were fabricated and evaluated as tissue engineering scaffolds for cartilage regeneration in vitro and in vivo. The crosslinker for the gelatin component was selected among glutaraldehyde, bisepoxy, and a water-soluble carbodiimide (WSC) based upon the proliferation of chondrocytes on the crosslinked gelatin. WSC was found to be the most suitable crosslinker. Complex scaffolds made from chitosan and gelatin with a component ratio equal to one possessed the proper degradation rate and mechanical stability in vitro. Chondrocytes were able to proliferate well and secrete abundant extracellular matrix in the chitosan-gelatin (1:1) complex scaffolds crosslinked by WSC (C1G1WSC) compared to the non-crosslinked scaffolds. Implantation of chondrocytes-seeded scaffolds in the defects of rabbit articular cartilage confirmed that C1G1WSC promoted the cartilage regeneration. The neotissue formed the histological feature of tide line and lacunae in 6.5 months. The amount of glycosaminoglycans in C1G1WSC constructs (0.187±0.095 µg/mg tissue) harvested from the animals after 6.5 months was 14 wt.% of that in normal cartilage (1.329±0.660 µg/mg tissue). The average compressive modulus of regenerated tissue at 6.5 months was about 0.539 MPa, which approached to that of normal cartilage (0.735 MPa), while that in the blank control (3.881 MPa) was much higher and typical for fibrous tissue. Type II collagen expression in C1G1WSC constructs was similarly intense as that in the normal hyaline cartilage. According to the above results, the use of C1G1WSC scaffolds may enhance the cartilage regeneration in vitro and in vivo.

Effects of types and length of soft-segments on the physical properties and blood compatibility of polyurethanes.

Segmented polyurethane (SPU) materials based on different soft-segment component (PPG, PTMO and PBA) and various length of soft-segment (molecular weight of PBA: 500, 700 and 1000) were synthesized in this research. The soft-segment components were synthesized from polyether-polyols (PPG and PTMO) or from polyester-polyol (PBA). The physical properties and structure characterization of the synthesized SPUs were fully investigated using differential scanning calorimetry (DSC) analysis, and stress-strain measurements. Blood compatibility was evaluated with the platelet adhesion ratio (PAR) and the morphological observation for adhering platelets. Our results showed that the physical properties and blood compatibility of SPUs were closely related to its composition, which was controlled by (1) the types of the soft-segment component employed and (2) the length of soft segments. Polyether-polyol-based SPUs exhibited greater phase separations, poorer tensile strengths, and better blood compatibility, compared with polyester-polyol-based SPUs. SPUs with shorter soft-segment component exhibited greater phase mixing, higher tensile strength, but lower blood compatibility of SPUs, as compared with its counterparts with longer soft-segment component.

A novel urethane acrylate-based root canal sealer with improved degree of conversion, cytotoxicity, bond strengths, solubility, and dimensional stability.

INTRODUCTION: We have developed new urethane acrylate-based root canal sealers using polycarbonate (PC) as polyol and 2,2-azobis(2-methyl)butyronitrile (AMBN) as a thermal initiator. The purpose of this study was to compare the properties among a group of seven sealers: (1) polybutyleneadipate (PBA) with 2,2-azobis-isobutyronitrile (AIBN), (2) PBA-AMBN, (3) PC-AIBN, (4) PC-AMBN, (5) AH Plus (Dentsply DeTrey GmbH, Konstanz, Germany), (6) Epiphany (Pentron Clinical Technologies, Wallingford, CT), and (7) EndoREZ (Ultradent Products, Inc, South Jordan, UT). METHODS: Attenuated total reflectance-Fourier transforming infrared spectroscopy was used to analyze the degree of conversion. Cytotoxicity was evaluated using MTT assay. In addition, push-out bond strength, solubility, and dimensional stability were investigated. RESULTS: Urethane acrylate-based root canal sealers behaved better than Epiphany and EndoREZ for the properties evaluated in this study. The PC-AMBN sealer exhibited the highest degree of conversion even in the apical third, and its cytotoxicity for nonsetting and aged specimens at 24 hours was comparable to AH Plus sealer. In addition, the PC-AMBN sealer with zinc oxide/thermoplastic polyurethane cones had a significantly higher bond strength than AH Plus with gutta percha. Solubility and dimensional changes of the PC-AMBN sealer conformed to the American National Standards Institute/American Dental Association (ANSI/ADA) standard 57. CONCLUSIONS: The PC-AMBN sealer has great potential for use in endodontic therapy.

Kinetic study of acid depolymerization of chitosan and effects of low molecular weight chitosan on erythrocyte rouleaux formation.

In this study, the depolymerization of chitosan was carried out in an acetic acid aqueous solution and was followed by viscometry for molecular weight determination. It was found that the depolymerization rate increased with elevated temperatures and with high acid concentrations. Based on FTIR analysis, the chitosan was depolymerized randomly along the backbone; no other structural change was observed during the acid depolymerization process. Revealed in the TGA study, the degradation temperature and char yield of LMWCs (low molecular weight chitosan) were molecular weight dependent. The blood compatibility of LMWCs was also investigated: rouleaux formation was observed when erythrocyte contacted with LMWCs, which showed that LMWCs are able to interfere with the negatively charged cell membrane through its polycationic properties. Furthermore, as regards a kinetics investigation, the values of M(n) (number-average molecular weight) were obtained from an experimentally determined relationship. The kinetics study showed that the complex salt, formed by amine on chitosan and acetic acid, acted as catalyst. Finally, the activation energy for the hydrolysis of the glycosidic linkage on chitosan was calculated to be 40kJ/mol; the mechanism of acid depolymerization is proposed. In summary, LMWCs could be easily and numerously generated with acid depolymerization for further biological applications.

Antibacterial activity and biocompatibility of a chitosan-gamma-poly(glutamic acid) polyelectrolyte complex hydrogel.

In this study, we prepared a polyelectrolyte complex (PEC) hydrogel comprising chitosan as the cationic polyelectrolyte and gamma-poly(glutamic acid) (gamma-PGA) as the anionic polyelectrolyte. Fourier transform infrared spectroscopy revealed that ionic complex interactions existed in the chitosan-gamma-PGA PEC hydrogels. The compressive modulus increased upon increasing the degree of complex formation in the chitosan-gamma-PGA PEC hydrogel; the water uptake decreased upon increasing the degree of complex formation. At the same degree of complex formation, the compressive modulus was larger for the chitosan-dominated PEC hydrogels; the water uptake was larger for the gamma-PGA-dominated ones. Scanning electron microscopy images revealed the existence of interconnected porous structures (pore size: 30-100mum) in all of the chitosan-gamma-PGA PEC hydrogels. The chitosan-gamma-PGA PEC hydrogels also exhibited antibacterial activity against Escherichia coli and Staphylococcus aureus. In addition, in vitro cell culturing of 3T3 fibroblasts revealed that all the chitosan-gamma-PGA PEC hydrogels were effective in promoting cell proliferation, especially the positively charged ones (chitosan-dominated). Therefore, the chitosan-gamma-PGA polyelectrolyte hydrogel appears to have potential as a new material for biomedical applications.

Morphological control of the electrochemically deposited poly(4-vinyltriphenylamines) (PVTPAs).

The morphology of the thin films obtained from electrochemical deposition of poly(4-vinyltriphenylamine)s (PVTPAs) on ITO surface varies as their molecular weight increases. The SEM studies revealed that while uniform coating could be obtained from low molecular weight PVTPAs (approximately 2700), uneven and rough coating with numerous cracks on the surface would be formed from high molecular weight PVTPAs. These defects could be reduced by using our surface modification strategy, in which the ITO surface was first primed with a thin layer of electrochemical coating of poly(methylenetriphenylamine) (PMTPA). This coating would turn the highly polar ITO surface into a nonpolar conducting surface that benefits for the PVTPA deposition. Our electroluminescence test suggested that this type of PMTPA/PVTPA composite film is good for hole injection and transportation.

Fast fabrication of integrated surface-relief and particle-diffusing plastic diffuser by use of a hybrid extrusion roller embossing process.

Most plastic diffusers are either of surface-relief or particle-diffusing types, based on different principles and fabrication methods. This paper reports an innovative extrusion roller embossing process, which enables the fabrication of diffusers with both surface-relief and particle-diffusing functions. An extruder with die is employed to fabricate the thin film of PC/bead composite; the roller micro-embossing process is used to replicate the microstructure onto the surface of PC composite film. A metallic roller mold with microstructures is fabricated using turning process. During the extrusion rolling embossing process, the extruded film of PC with diffusion beads is immediately pressed against the surface of the roller mold. Under the proper processing parameters, the plastic diffusers integrating surface-relief and particle-diffusing functions have been successfully fabricated. The shape, uniformity, and optical properties of fabricated diffuser have been verified. This method shows the great potential for continuous fabrication of high-performance plastic diffusers integrating surface-relief and particle-diffusing functions with high throughput.

A novel polyurethane-based root canal-obturation material and urethane-acrylate-based root canal sealer-part 2: evaluation of push-out bond strengths.

We have developed a visible-light curable urethane-acrylate/tripropylene glycol diacrylate (UA/TPGDA) oligomer to serve as a root canal sealer and a zinc oxide/thermoplastic polyurethane (ZnO/TPU) composite to serve as a root canal obturation material. The purpose of this study was to compare the push-out bond strengths of the following 8 groups of materials: (1) Tubliseal + gutta-percha (TB/GP); (2) Tubliseal + Resilon (TB/R); (3) Epiphany + gutta-percha (EP/GP); (4) Epiphany + Resilon (EP/R); (5) EndoREZ sealer + EndoREZ cone (ES/EC); (6) EndoREZ sealer + ZnO/TPU (ES/PU); (7) UA/TPGDA + EndoREZ cone (UA/EC); and (8) UA/TPGDA + ZnO/TPU (UA/PU). Eighty 1-mm-thick root slices prepared from extracted human permanent molars were randomly divided into 8 groups with 10 specimens in each group. Root slices were filled with the above obturation materials, and then push-out test was performed with a universal testing machine. The results showed that the UA/EC and UA/PU groups had significantly higher bond strengths than the other groups.

A novel polyurethane-based root canal-obturation material and urethane acrylate-based root canal sealer--part I: synthesis and evaluation of mechanical and thermal properties.

Resilon (RealSeal; SybronEndo, Orange, CA) has been developed as an alternative to gutta percha, but its advantages over gutta percha remain controversial. In this study, we developed a novel zinc oxide/thermoplastic polyurethane (ZnO/TPU) composite root canal-filling material and a visible-light curable urethane-acrylate/tripropylene glycol diacrylate (UA/TPGDA) root canal sealer. The mechanical and thermal properties of the ZnO/TPU composite were compared with those of gutta percha and Resilon. Results showed that the tensile strength and elastic modulus of the ZnO/TPU composite were markedly higher than those of gutta percha and Resilon. The melting points of all three materials were similar; however, the enthalpy change and specific heat of ZnO/TPU (9.4 J/g, 0.7 J/g degrees C) were close to those of gutta percha (10.9 J/g, 0.7 J/g degrees C) but lower than those of Resilon (28.9 J/g, 1.3 J/g degrees C). The results indicate that ZnO/TPU composite exhibits better mechanical strength than Resilon, and its combination with UA/TPGDA sealer has excellent potential to be used as a root canal-filling material.

Magnetic SiO(2)/Fe(3)O(4) colloidal crystals.

We proposed a novel technique to fabricate colloidal crystals by using monodisperse SiO(2) coated magnetic Fe(3)O(4)(SiO(2)/Fe(3)O(4)) microspheres. The magnetic SiO(2)/Fe(3)O(4) microspheres with a diameter of 700 nm were synthesized in the basic condition with ferric sulfate, ferrous sulfate, tartaric acid and tetraethyl orthosilicate (TEOS) in the reaction system. Monodisperse SiO(2)/Fe(3)O(4) superparamagnetic microspheres have been successfully used to fabricate colloidal crystals under the existing magnetic field.

Rapid fabrication of 2D and 3D photonic crystals and their inversed structures.

In this paper a new technique is proposed for the fabrication of two-dimensional (2D) and three-dimensional (3D) photonic crystals using monodisperse polystyrene microspheres as the templates. In addition, the approaches toward the creation of their corresponding inversed structures are described. The inversed structures were prepared by subjecting an introduced silica source to a sol-gel process; programmed heating was then performed to remove the template without spoiling the inversed structures. Utilizing these approaches, 2D and 3D photonic crystals and their highly ordered inversed hexagonal multilayer or monolayer structures were obtained on the substrate.

Fabrication of polymer microlens arrays using capillary forming with a soft mold of micro-holes array and UV-curable polymer.

This paper reports a simple and effective method to fabricate microlens arrays with the ultraviolet-curable resins, and a soft mold of micro-holes array. During capillary forming operation, the surface of the soft mold of micro-holes array is being pressed against the ultraviolet-curable resin layer coated on the plastic substrate. An array of convex lense can be formed in the circular holes of the soft mold due to the capillary filling and surface tension. The microlens arrays have smooth surface and uniform focusing function. The shape and height of micolens can be controlled with a proper combination of pressing pressure, pressing duration and UV curing dose. This technique shows great potential for fabricating polymer microlens arrays with high productivity and low cost.