Electrospun PELCL membranes loaded with QK peptide for enhancement of vascular endothelial cell growth

One of the major challenges in tissue engineering of small-diameter vascular grafts is to inhibit intimal hyperplasia and keep long-term patency after implantation. Rapid endothelialization of the grafts could be an effective approach. In this study, QK, a peptide mimicking vascular endothelial growth factor, was selected as the bioactive substrate and loaded in electrospun membranes for enhancement of vascular endothelial cell growth. In detail, QK peptide was firstly introduced with poly(ethylene glycol) diacrylate into a thiolated chitosan solution that could transfer into hydrogel. Then, suspensions or emulsions of poly(ethylene glycol)-b-poly(l-lactide-co-ε-caprolactone) (PELCL) containing QK peptide (with or without chitosan hydrogel) were electrospun into fibrous membranes. For comparison, the electrospun PELCL membrane without QK was also fabricated. Results of release behaviors showed that the electrospun membranes, especially that contained chitosan hydrogel prepared by suspension electrospinning, could successfully encapsulate QK peptide and maintain its secondary structure after released. In vitro cell culture studies exhibited that the release of QK peptide could accelerate the proliferation of vascular endothelial cells in the 9 days. It was suggested that the electrospun PELCL membranes loaded with QK peptide might have potential applications in vascular tissue engineering.     

A multisource energy harvesting utilizing highly efficient ferroelectric PMN-PT single crystal

This paper demonstrates a multi-source energy harvester that is able to utilize simultaneously both piezoelectric and pyroelectric effects in lead magnesium niobate-lead titanate (PMN-PT) single crystal. The paper presents a study of PMN-PT single crystal with a (67:33) composition grown in our laboratory via a vertical gradient freeze method without any flux. The performance of the piezoelectric and pyroelectric energy harvester using unimorph device structure was evaluated via modeling and experiment. The theoretical study was implemented based on a distributed parameter electromechanical model and the modelling procedure was approximated using finite element analysis to predict the electromechanical behavior of the harvester. The maximum power density at a resonance frequency of 50 Hz and optimum resistance of 2 MΩ was 16.7 nW/(g² cm³) under a 1 g acceleration of vibration. The measured values of electrical output parameters were in good agreement with theoretical and modelling results using MATLAB and COMSOL Multiphysics, respectively. By using the pyroelectric effect along with the piezoelectric effect, the output voltage of the energy harvester was found to be enhanced at the optimum resistance and specific frequency values. It was noticed that the output voltage was increased monotonically with temperature-difference (ΔT) and reaches up to 180 % of its original value under temperature difference of 1.7 °C at a frequency value of 49 Hz.     

Tuning the temperature coefficient of resonant frequency for 8-layer twinned hexagonal perovskite Ba<Subscript>8</Subscript>ZnTa<Subscript>6</Subscript>O<Subscript>24</Subscript> ceramics

High-Q dielectric materials ilmenite MgTiO₃, columbite MgNb₂O₆ and cubic perovskite Ba₃NiTa₂O₉ with negative temperature coefficient of resonant frequency (τ _f ) were selected as candidates for compensating the τ _f of hexagonal perovskite Ba₈ZnTa₆O₂₄. X-ray diffraction data shows that Ba₈ZnTa₆O₂₄ coexists with Ba₃NiTa₂O₉ but is not compatible with MgTiO₃ and MgNb₂O₆ at high temperature. The τ _f for the mixed hexagonal/cubic perovskite Ba₈ZnTa₆O₂₄–Ba₃NiTa₂O₉ system is tunable via the temperature compensation effect and its quality factor may be improved via annealing the ceramics at high temperature to enhance the cation ordering in the cubic component. Permittivity ε _r  ~ 22–25, Q×f > 30,000 GHz and tunable τ _f within ±10 ppm/°C were achieved in the range of about 50–80 wt% Ba₃NiTa₂O₉ for the hexagonal/cubic perovskite composite Ba₈ZnTa₆O₂₄–Ba₃NiTa₂O₉ ceramics, which is suitable for the application as dielectric resonators and filters.     

Indium selenide microrod films: chemical bath deposition from acidic bath

Films of indium selenide was deposited onto glass and indium tin oxide coated glass substrates in acidic medium using chemical bath deposition at room temperature. Indium sulphate and sodium selenosulphate were used as precursors of In³⁺ and Se^2?, respectively. The structural, surface morphological and optical properties of the deposited films were studied. Diffractograms in structural study revealed the deposited material is In₂Se₃ films. Controlled bath conditions resulted in the evolution of the In₂Se₃ microrod-like morphology. The optical band gap of the film was found to be 1.7 eV.     

Effects of PNN/PZT ratios on phase structure,electric properties and relaxation behavior of PZN–PNN–PZT ceramics

Pb(Zn_1/3Ni_2/3)_c(Ni_1/3Nb_2/3)_a(Zr_xTi_y)_bO₃ (PZN–PNN–PZT, the ratios of PNN/PZT a/b were 0.88, 1 and 1.136) piezoelectric ceramics were prepared by a traditional solid-state reaction method. The effects of PNN/PZT ratio on phase structure, microstructure and electric properties as well as the relaxation behaviors of PZN–PNN–PZT ceramics were investigated. The XRD patterns showed that all ceramics samples had a pure perovskite phase structure. Meanwhile, it was found that the phase structure undergoes a tetragonal, tetragonal-rhombohedral to rhombohedral transition as ratios of PNN/PZT increased. With the increasing of a/b from 0.88 to 1.136, the dielectric constant and diffusive phase coefficient decreases, it was indicated that relaxation behaviors also decreased. When ceramics with a/b was 1.136, the dielectric relaxation γ reached the minimum and electrical properties were poor. The electric properties of ceramics with a/b was 1.00 have an excellent properties, it was indicated that ceramics reached an optimization at the MPB structure.     

Novel method to transform ZnO nanorods into interlaced tattered nanosheets by changing the target inclination angle

ZnO nanoparticles were synthesized by liquid-phase pulse laser ablation of a Zn foil target immersed in deionized water. Nanosecond Q-switched Nd:YAG laser pulses of 532 nm were applied to the Zn foil target at a perpendicular and inclined (θ = 45°) angles. X-ray diffraction analysis revealed that both cases feature a ZnO nanostructure with a hexagonal wurtzite structure and that the particle size increases with the inclined target angle. Field emission scanning electron microscopy results of a colloidal drop cast on a glass substrate showed the ZnO has a nanorod structure in the case of a perpendicular target angle and an interlaced tattered nanosheet structure in the case of an inclined target angle. Photoluminescence spectra showed emission peaks in the UV, violet, blue, and green spectral regions, which correspond to excitonic and various defects resulting in an enhancement of emissions at inclined target angle.     

Microstructure and fracture behavior of non eutectic Sn–Bi solder alloys

The microstructure and mechanical properties of Sn–xBi (x = 10, 20, 25, and 35) solder alloy were investigated by scanning electronic microscope and notch tensile test. The results showed that the microstructure of Sn–10Bi and Sn–20Bi solder alloy was constituted by Bi particle and β-Sn phase. The microstructure of Sn–25Bi and Sn–35Bi solder alloy was consisted of eutectic phase and primary phase. The ultimate tensile load of Sn–20Bi solder alloy was higher than that of Sn–10Bi in notch tensile test. The ultimate tensile load of Sn–25Bi and Sn–35Bi was declined gradually compared with that of Sn–20Bi solder alloy. The fracture energy of Sn–xBi was decreased continuously when the Bi fraction increased. Crack observation, fracture surface observation, and finite element analysis revealed that the crack initiation and propagation of Sn–25Bi and Sn–35Bi was dominated by the fracture of brittle eutectic phase. Therefore, the ultimate tensile load and fracture energy of Sn–25Bi and Sn–35Bi were damaged compared with that of Sn–20Bi.     

Biocompatible nano-gallium/hydroxyapatite nanocomposite with antimicrobial activity

Intensive research in the area of medical nanotechnology, especially to cope with the bacterial resistance against conventional antibiotics, has shown strong antimicrobial action of metallic and metal-oxide nanomaterials towards a wide variety of bacteria. However, the important remaining problem is that nanomaterials with highest antibacterial activity generally express also a high level of cytotoxicity for mammalian cells. Here we present gallium nanoparticles as a new solution to this problem. We developed a nanocomposite from bioactive hydroxyapatite nanorods (84?wt %) and antibacterial nanospheres of elemental gallium (16?wt %) with mode diameter of 22?±?11?nm. In direct comparison, such nanocomposite with gallium nanoparticles exhibited better antibacterial properties against Pseudomonas aeruginosa and lower in-vitro cytotoxicity for human lung fibroblasts IMR-90 and mouse fibroblasts L929 (efficient antibacterial action and low toxicity from 0.1 to 1?g/L) than the nanocomposite of hydroxyapatite and silver nanoparticles (efficient antibacterial action and low toxicity from 0.2 to 0.25?g/L). This is the first report of a biomaterial composite with gallium nanoparticles. The observed strong antibacterial properties and low cytotoxicity make the investigated material promising for the prevention of implantation–induced infections that are frequently caused by P. aeruginosa.     

Effect of bioactive dental adhesive on periodontal and endodontic pathogens

The objectives of this study were to: (1) develop a new bioactive dental bonding agent with nanoparticles of amorphous calcium phosphate and dimethylaminohexadecyl methacrylate for tooth root caries restorations and endodontic applications, and (2) investigate biofilm inhibition by the bioactive bonding agent against eight species of periodontal and endodontic pathogens for the first time. Bonding agent was formulated with 5?% of dimethylaminohexadecyl methacrylate. Nanoparticles of amorphous calcium phosphate at 30?wt% was mixed into adhesive. Eight species of biofilms were grown on resins: Porphyromonas gingivalis, Prevotella intermedia, Prevotella nigrescens, Aggregatibacter actinomycetemcomitans, Fusobacterium nucleatum, Parvimonas micra, Enterococcus faecalis, Enterococcus faecium. Colony-forming units, live/dead assay, biomass, metabolic activity and polysaccharide of biofilms were determined. The results showed that adding dimethylaminohexadecyl methacrylate and nanoparticles of amorphous calcium phosphate into bonding agent did not decrease dentin bond strength (P?>?0.1). Adding dimethylaminohexadecyl methacrylate reduced the colony-forming units of all eight species of biofilms by nearly three orders of magnitude. The killing efficacy of dimethylaminohexadecyl methacrylate resin was: P. gingivalis?>?A. actinomycetemcomitans?>?P. intermedia?>?P. nigrescens?>?F. nucleatum?>?P. micra?>?E. faecalis?>?E. faecium. Dimethylaminohexadecyl methacrylate resin had much less biomass, metabolic activity and polysaccharide of biofilms than those without dimethylaminohexadecyl methacrylate (P?<?0.05). In conclusion, a novel dental adhesive was developed for root caries and endodontic applications, showing potent inhibition of biofilms of eight species of periodontal and endodontic pathogens, and reducing colony-forming units by three orders of magnitude. The bioactive adhesive is promising for tooth root restorations to provide subgingival margins with anti-periodontal pathogen capabilities, and for endodontic sealer applications to combat endodontic biofilms.     

Effect of stents coated with a combination of sirolimus and alpha-lipoic acid in a porcine coronary restenosis model

The aim of this study was to evaluate antiproliferative sirolimus- and antioxidative alpha-lipoic acid (ALA)-eluting stents using biodegradable polymer [poly-l-lactic acid (PLA)] in a porcine coronary overstretch restenosis model. Forty coronary arteries of 20 pigs were randomized into four groups in which the coronary arteries had a bare metal stent (BMS, n = 10), ALA-eluting stent with PLA (AES, n = 10), sirolimus-eluting stent with PLA (SES, n = 10), or sirolimus- and ALA-eluting stent with PLA (SAS, n = 10). A histopathological analysis was performed 28 days after the stenting. The ALA and sirolimus released slowly over 30 days. There were no significant differences between groups in the injury or inflammation score; however, there were significant differences in the percent area of stenosis (56.2 ± 11.78 % in BMS vs. 51.5 ± 12.20 % in AES vs. 34.7 ± 7.23 % in SES vs. 28.7 ± 7.30 % in SAS, P < 0.0001) and fibrin score [1.0 (range 1.0–1.0) in BMS vs. 1.0 (range 1.0–1.0) in AES vs. 2.0 (range 2.0–2.0) in SES vs. 2.0 (range 2.0–2.0) in SAS, P < 0.0001] between the four groups. The percent area of stenosis based on micro-computed tomography corresponded with the restenosis rates based on histopathological stenosis in different proportions in the four groups (54.8 ± 7.88 % in BMS vs. 50.4 ± 14.87 % in AES vs. 34.5 ± 7.22 % in SES vs. 28.9 ± 7.22 % in SAS, P < 0.05). SAS showed a better neointimal inhibitory effect than BMS, AES, and SES at 1 month after stenting in a porcine coronary restenosis model. Therefore, SAS with PLA can be a useful drug combination for coronary stent coating to suppress neointimal hyperplasia.