Silver coated bioactive glass particles for wound healing applications

Bioactive glass particles (0.42SiO₂–0.15CaO–0.23Na₂O–0.20ZnO) of varying size (<90 μm and 425–850 μm) were synthesized and coated with silver (Ag) to produce Ag coated particles (PAg). These were compared against the uncoated analogous particles (Pcon.). Surface area analysis determined that Ag coating of the glass particles resulted in increased the surface area from 2.90 to 9.12 m²/g (90 μm) and 1.09–7.71 m²/g (425–850 μm). Scanning electron microscopy determined that the Ag coating remained at the surface and there was little diffusion through the bulk. Antibacterial (Escherichia coli—13 mm and Staphylococcus epidermidis—12 mm) and antifungal testing (Candida albicans—7.7 mm) determined that small Ag-coated glass particles exhibited the largest inhibition zones compared to uncoated particles. pH analysis determined an overall higher pH consider in the smaller particles, where after 24 h the large uncoated and Ag coated particles were 8.27 and 8.74 respectively, while the smaller uncoated and Ag coated particles attained pH values of 9.63 and 9.35 respectively.     

PEG-grafted chitosan nanoparticles as an injectable carrier for sustained protein release

The development of injectable nanoparticulate “stealth” carriers for protein delivery is a major challenge. The objective of this work was to investigate the possibility of achieving the controlled release of a model protein, insulin, from PEG-grafted chitosan (PEG-g-chitosan) nanoparticles (mean diameter 150–300 nm) prepared by the ion gelation method. Insulin was efficiently incorporated into the nanoparticles, and reached as high as 38%. In vitro release showed that it could control the insulin release by choosing the composition, loading and release temperature. We observed that the composition of the nanoparticle surface (C/O ratio) increased from 2.40 to 3.23, with an increase in the incubation time. Therefore, we concluded that during this time, insulin release from PEG-g-chitosan nanoparticles followed a diffusion mechanism in which erosion was negligible. The experiments also demonstrated that PEG-g-chitosan helped to maintain the natural structure of the protein entrapped in the nanoparticles.     

Surface characterization of plasma-treated and PEG-grafted PDMS for micro fluidic applications

The contact angle measurements have shown that polydimethyl siloxane (PDMS) surfaces treated by air plasma can recover up to about 40% of its hydrophobic nature in less than 20 min of air exposure. Therefore, poly(ethylene glycol) (PEG) silane was grafted after plasma treatment to permanently change the PDMS surface as hydrophilic in nature for micro fluidic application. The surface chemistry of plasma-treated and PEG-grafted PDMS substrate has been studied using X-ray photoelectron spectroscopy (XPS). The proportion of carbon atoms as C-Si and hydrocarbon decreased for both plasma-treated as well as PEG-grafted PDMS surfaces. The plasma treatment had increased the proportion of carbon atoms as CO and C(O)OX in C1s, whereas grafting of PEG silane decreased the proportion of C(O)OX and an increase in C-OX and CO functionalities. This is due to the interaction of OCH₃ on Si (in PEG silane) with C-OX and C(O)OX on plasma-treated PDMS by covalent bonding. Therefore, an increase in CO and C-OX functionalities and relative decrease in C(O)OX is expected. The plasma treatment of micro channels had increased the fluid velocity by a factor or four and similar measurements were observed in PEG grafted micro channel in PDMS chip. This indicates that the fluid velocity depends on the hydrophilic nature of substrate. The effect of nature of fluids on the fluid velocity in PDMS-based micro channel was also studied. It was observed that the fluid velocity was decreased with decreasing the pH values of the fluid.     

Silver nanoparticles deposited on porous silicon as a surface-enhanced Raman scattering (SERS) active substrate

Silver nanoparticles were deposited spontaneously from their aqueous solution on a porous silicon (PS) layer. The PS acts both as a reducing agent and as the substrate on which the nanoparticles nucleate. At higher silver ion concentrations, layers of nanoparticle aggregates were formed on the PS surface. The morphology of the metallic layers and their SERS activity were influenced by the concentrations of the silver ion solutions used for deposition. Raman measurements of rhodamine 6G (R6G) and crystal violet (CV) adsorbed on these surfaces showed remarkable enhancement of up to about 10 orders of magnitude.     

Paper-based SERS swab for rapid trace detection on real-world surfaces

One of the important but often overlooked considerations in the design of surface-enhanced Raman scattering (SERS) substrates for trace detection is the efficiency of sample collection. Conventional designs based on rigid substrates such as silicon, alumina, and glass resist conformal contact with the surface under investigation, making the sample collection inefficient. We demonstrate a novel SERS substrate based on common filter paper adsorbed with gold nanorods, which allows conformal contact with real-world surfaces, thus dramatically enhancing the sample collection efficiency compared to conventional rigid substrates. We demonstrate the detection of trace amounts of analyte (140 pg spread over 4 cm2) by simply swabbing the surface under investigation with the novel SERS substrate. The hierarchical fibrous structure of paper serves as a 3D vasculature for easy uptake and transport of the analytes to the electromagnetic hot spots in the paper. Simple yet highly efficient and cost-effective SERS substrate demonstrated here brings SERS-based trace detection closer to real-world applications.     

Preparation and characterization of bioactive glass nanoparticles prepared by sol-gel for biomedical applications

Bioactive glass nanoparticles (BG-NPs), based on both ternary (SiO(2)-CaO-P(2)O(5)) and binary (SiO(2)-CaO) systems, were prepared via an optimized sol-gel method. The pH of preparation and the effect of heat treatment temperature were evaluated, as well as the effect of suppressing P in the bioactivity ability of the materials. The morphology and composition of the BG-NPs were studied using FTIR, XRD and SEM. The bioactive character of these materials was accessed in?vitro by analyzing the ability for apatite formation onto the surface after being immersed in simulated body fluid (SBF). XRD, EDX and SEM were used to confirm the bioactivity of the materials. The BG-NP effect on cell metabolic activity was assessed by seeding L929 cells with their leachables, proving the non-cytotoxicity of the materials. Finally the most bioactive BG-NPs developed (ternary system prepared at pH?11.5 and treated at 700?°C) were successfully combined with chitosan in the production of biomimetic nanocomposite osteoconductive membranes that could have the potential to be used in guided tissue regeneration.     

Synthesis and characterization of manganese containing mesoporous bioactive glass nanoparticles for biomedical applications

Mesoporous bioactive glass (BG) nanoparticles based in the system: SiO₂–P₂O₅–CaO–MnO were synthesized via a modified Stöber process at various concentrations of Mn (0–7 mol %). The synthesized manganese-doped BG nanoparticles were characterized in terms of morphology, composition, in vitro bioactivity and antibacterial activity. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET) analysis confirmed that the particles had spherical morphology (mean particle size: 110?nm) with disordered mesoporous structure. Energy dispersive X-ray spectroscopy (EDX) confirmed the presence of Mn, Ca, Si and P in the synthesized Mn-doped BG particles. Moreover, X-ray diffraction (XRD) analysis showed that Mn has been incorporated in the amorphous silica network (bioactive glass). Moreover, it was found that manganese-doped BG particles form apatite crystals upon immersion in simulated body fluid (SBF). Inductively coupled plasma atomic emission spectroscopy (ICP-OES) measurements confirmed that Mn is released in a sustained manner, which provided antibacterial effect against Bacillus subtilis, Pseudomonas aeruginosa and Staphylococcus aureus. The results indicate that the incorporation of Mn in the bioactive glass network is an effective strategy to develop novel multifunctional BG nanoparticles for bone tissue engineering.     

In-situ partial sintering of gold-nanoparticle sheets for SERS applications

A new, versatile substrate design for surface-enhanced Raman spectroscopy (SERS) is introduced that provides better illumination and collection efficiency than other solid substrates. It uses sheets of 5 nm diameter gold nanoparticles that are draped by drying-mediated self-assembly onto 100 nm thick silicon nitride membranes. During laser illumination, partial in-situ sintering of the nanoparticles into larger structures with tiny gaps (≈2 nm) greatly increases the SERS enhancement factor. The detection of 1 pM of p-mercaptoaniline and 1 fg of 2,4-dinitrotoluene is demonstrated. The use of self-assembled nanoparticle sheets furthermore makes it possible to perform SERS detection in situ on top of a probe solution droplet.     

Modification of porous calcium phosphate surfaces with different geometries of bioactive glass nanoparticles

In this study, the effects of bioactive glass nanoparticles' (nBGs) size and shape incorporated into hydroxyapatite/β-tricalcium phosphate (BCP) scaffolds were investigated. We prepared a highly porous (> 85%) BCP scaffold and coated its surface with a nanocomposite layer consisted of polycaprolactone (PCL) and rod (~ 153 nm in height and ~ 29 nm in width) or spherical (~ 33 nm and 64 nm in diameter) nBGs. Osteogenic gene expression by primary human osteoblast-like cells (HOB) was investigated using quantitative real time polymerase chain reaction (q-RT-PCR). We demonstrated for the first time that in vitro osteogenesis is dramatically affected by the shape of the nBGs, whereby rod shaped nBGs showed the most significant osteogenic induction, compared to spherical particles (regardless of their size). Importantly, the good biological effect observed for the rod shaped nBGs was coupled by a marked increase in the modulus (~ 48 MPa), compressive strength (~ 1 MPa) and failure strain (~ 6%), compared to those for the BCP scaffolds (~ 4 MPa, ~ 1 MPa and ~ 0.5% respectively). The findings of this study demonstrated that the shape of the nBGs is of significant importance when considering bone regeneration.     

银纳米颗粒单层膜的组装及其SERS特性研究

用柠檬酸三钠还原硝酸银制备银溶胶,再添加己烷和乙醇,银纳米颗粒会组装在水面上。利用LB拉膜机滑障沿水面压缩银纳米颗粒,使得银纳米颗粒紧密有序地排列在水面上。把这层银纳米颗粒转移到硅衬底上,即得到一种密集排列的银纳米颗粒单层膜SERS基底,采用扫描电子显微镜（SEM）研究该基底的表面形貌,并以罗丹明6G（Rh6G）作为探针分子检测其SERS活性,结果表明,银纳米颗粒具有较好的均一性和聚集度,且Rh6G在该单层膜基底上得到了非常好的SERS效应。     

New target materials for innovative applications on glass

In the new emerging markets of flat panel display, photovoltaic and optical coating applications, the introduction of cylindrical rotating magnetron technology can accommodate the needs for faster, better and cheaper coating processes. Recent developments of hardware (compact end blocks, etc.) and target materials for rotatable magnetron technology offer a total solution to the innovative thin film applications.     

Strengthening coating based on silica nanoparticles for soda-lime-silica glass

We have developed a strengthening coating based on silica nanoparticles for soda-lime-silica glass, examined conditions for the synthesis of SiO₂ particles with tailored structure and application of coating of necessary thickness to glass through adsorption from solution, and optimized heat treatment of the coated glass. The nanohardness and centrosymmetric bending strength of the coated glass have been measured, and the mechanism behind the coating-induced increase in glass strength is discussed.     

Absorption mapping for characterization of glass surfaces

The surface quality of bare substrates and preparation procedures take on an important role in optical coating performances. The most commonly used techniques of characterization generally give information about roughness and local defects. A photothermal deflection technique is used for mapping surface absorption of fused-silica and glass substrates. We show that absorption mapping gives specific information on surface contamination of bare substrates. We present experimental results concerning substrates prepared by different cleaning and polishing techniques. We show that highly polished surfaces lead to the lowest values of residual surface absorption. Moreover the cleaning behavior of surfaces of multicomponent glasses and their optical performance in terms of absorption are proved to be different from those of fused silica.     

Chitosan-coated anisotropic silver nanoparticles as a SERS substrate for single-molecule detection

Surface-enhanced Raman spectroscopy (SERS) is a technique that has become widely used for identifying and providing structural information about molecular species in low concentration. There is an ongoing interest in finding optimum particle size, shape and spatial distribution for optimizing the SERS substrates and pushing the sensitivity toward the single-molecule detection limit. This work reports the design of a novel, biocompatible SERS substrate based on small clusters of anisotropic silver nanoparticles embedded in a film of chitosan biopolymer. The SERS efficiency of the biocompatible film is assessed by employing Raman imaging and spectroscopy of adenine, a significant biological molecule. By combining atomic force microscopy with SERS imaging we find that the chitosan matrix enables the formation of small clusters of silver nanoparticles, with junctions and gaps that greatly enhance the Raman intensities of the adsorbed molecules. The study demonstrates that chitosan-coated anisotropic silver nanoparticle clusters are sensitive enough to be implemented as effective plasmonic substrates for SERS detection of nonresonant analytes at the single-molecule level.     

Enhancement of luminescence of Rhodamine B by gold nanoparticles in thin films on glass for active optical materials applications

Fluorescent dyes in solid matrices have many potential applications provided that their high optical efficiencies are achieved. We present here gold nanoparticles formed and incorporated together with fluorescent dye Rhodamine B into a film of polyvinyl alcohol (PVA). The increase of fluorescence of the dye results from its interaction with surface plasmons. The electric charge on the gold nanoparticles and the distance between them and the dye molecules has a significant effect on the fluorescence intensity. Fluorescence enhancement of 74% was achieved for the negatively charged particles. Dynamic measurements reveal decrease of fluorescent lifetimes of the dye in presence of gold nanoparticles. Our findings enable utilization of films with enhanced fluorescence in optical materials such as luminescence solar concentrators, solid state tunable laser and active waveguides.     

Semiconducting glass design for device applications

A method is presented by which stable amorphous semiconductors can be chosen for switching device applications. This method is based on the empirical relationship observed between the glass transition temperature, the band gap and the mean coordination number of covalent amorphous semiconductors. In particular, it is shown that tetrahedrally coordinated glasses with band gaps in the range 0.6–1.2 eV are excellent candidates for high reliability materials. One such material, a-CdAs₂, was studied in some detail and was found to be very stable and very easy to fabricate in thin film form. Both negative resistance and threshold switching devices were successfully fabricated with this material, and preliminary results from accelerated life testing are promising.     

Effect of coupling crater structure and Ag nanoparticles on SERS enhancement

Journal of Materials Science - This study was aimed at enhancing surface plasmon resonance through a combination of Ag nanoparticles (NPs) and an asymmetric crater structure capable of...     

Enhanced processing of coatings on glass surfaces

In this contribution, basic technically usable interactions of atmospheric pressure plasmas (APP), laser irradiation and solids as well as a technique which combines such plasmas and laser irradiation are introduced. Two examples for plasma‐enhanced laser processing of coatings on glass surfaces are presented in more detail. First, APP‐assisted annealing of amorphous silicon layers is discussed. It is shown that the crystallised area is notably increased by assisting plasmas where the particular improvement factor depends on the particularly applied type of plasma. Second, the impact of assisting plasmas on laser removal of lacquers and varnishes from glass surfaces is presented. By introducing a plasma jet to the laser removal process, the laser energy required for cleaning or delamination is notably reduced.