Silver-gold alloy nanoparticles biofabricated by fungal xylanases exhibited potent biomedical and catalytic activities.

The search for biocompatible nanoparticles with vast applicability has impacted on exploration of various biomaterials for the synthesis of mono and bimetallic nanoparticles. Xylanase is widely regarded as an industrially important enzyme but its potentials in nanotechnological applications are yet to be fully explored. The current study investigates the exploit of xylanases of Aspergillus niger L3 (NE) and Trichoderma longibrachiatum L2 (TE) produced through valorization of corn-cob, to synthesize silver-gold alloy nanoparticles (Ag-AuNPs). Characterization of the Ag-AuNPs involved UV-vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and field emission scanning electron microscopy and transmission electron microscopy, while their prospective use as antimicrobial, antioxidant, catalytic, anticoagulant, and thrombolytic agents were studied. The biosynthesized Ag-AuNPs were ruby red and light purple with surface plasmon resonance at 520 and 534 nm for NEAg-AuNPs and TEAg-AuNPs, respectively; while FTIR showed that protein molecules capped and stabilized the nanoparticles. The Ag-AuNPs were anisotropic with spherical, oval, and irregular shapes having sizes ranging from 6.98 to 52.51 nm. The nanoparticles appreciably inhibited the growth of tested clinical bacteria (23.40-90.70%) and fungi (70.10-89.05%), and also scavenged 2,2-diphenyl-1-picrylhydrazyl (48.51-53.79%) and hydrogen peroxide (80.5-95.50%). Furthermore, the Ag-AuNPs degraded malachite green (91.39%) and methylene blue (47.10%). Moreover, the Ag-AuNPs displayed outstanding anticoagulant and thrombolytic activities using human blood. This study further emphasizes the significance of xylanases in nanobiotechnology as it has established the potential of xylanases to synthesize Ag-AuNPs, which is being reported for the first time.

Fungal biomolecules assisted biosynthesis of Au-Ag alloy nanoparticles and evaluation of their catalytic property.

The catalytic reduction of methylene blue was studied using biosynthesised gold-silver (Au-Ag) alloy nanoparticles (NPs). The fungal biomass of Trichoderma harzianum was used as a reducing and stabilising agent in the synthesis of Au-Ag alloy NPs. The synthesised NPs were well characterised by UV-vis spectroscopy, dynamic light scattering, X-ray diffraction, transmission electron microscopy, energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The plausible synthesis mechanism involved in the formation of Au-Ag alloy NPs was also discussed with diagrammatic representation. A series of experiments was performed to investigate the catalytic activity of the as-prepared Au-Ag alloy NPs and found that the alloy NPs show excellent catalytic activity.

Interfacial properties and in vitro cytotoxic effects of surface-modified near infrared absorbing Au-Au(2)S nanoparticles.

Near infrared (NIR) absorbing Au-Au(2)S nanoparticles were modified with surfactants of different hydrocarbon chain lengths to allow loading of anticancer drug, cisplatin. The interfacial interactions and surfactant chain length effects on drug loading, optical properties and cytotoxicity were discussed in this work. Short-chain surfactants were oriented closer to the surface normal and were adsorbed at higher densities. Surface modification also changed the optical properties of the particles. Notably, particles modified with short-chain surfactants exhibited a red shift, whereas particles modified with long-chain surfactants showed a blue shift. The in vitro cytotoxicity of drug-loaded surface-modified particles was dependent on the surfactants' chain length. Significant cytotoxicity was observed for 1 mg/ml of drug-loaded particles using surfactants with the shortest chain length. After NIR triggered drug release, the released Pt compounds were observed to be cytotoxic, while remaining nanoparticles did not exhibit any cytotoxicity. Also, the released Pt compounds upon NIR irradiation of drug-loaded particles were observed to be more toxic and had a different molecular structure from cisplatin.

Corrosion of copper, nickel, and gold dental casting alloys: an in vitro and in vivo study.

The corrosion behavior of commercially available copper, nickel, and gold alloys for dental castings was investigated. The alloys investigated included: three copper alloys (76-87Cu, 6-11A1, 0-12Zn, 1-5Ni, 0-4Fe, 0.5-1.2Mn), two nickel alloys (68-78Ni, 12-16Cr, 4-14Mo, 0-1.7Be), and one gold alloy (77Au, 14Ag, 8Cu, 1Pd). Anodic and cathodic polarization curves, long-term immersion tests in saline and artificial saliva solutions, and dog crown studies were conducted to evaluate both the in vitro and in vivo corrosion characteristics of the alloys. All evaluations conducted demonstrated that the copper alloys were highly susceptible to corrosion attack. High corrosion currents were observed in the in vitro tests, and SEM of the alloys specimens showed significantly altered surfaces. The anodic polarization curves predicted that the beryllium-containing nickel alloy should be susceptible to localized corrosion and SEM revealed an etched surface with corrosion of certain microstructural features. No significant corrosion was predicted or observed for the non-beryllium nickel alloy and the gold alloy. The in vitro corrosion evaluations predicted the in vivo corrosion behavior for the alloys. Since the three copper alloys and the beryllium-containing nickel alloy demonstrated significant corrosion under the tested conditions, the use of these alloys for restorative procedures is questionable due to the release of significant levels of selected ions to the oral cavity.

Plaque accumulation on composite surfaces after various finising procedures.

A clinical study was undertaken to determine the rate at which plaque accumulates on the surfaces of composite restorations on which four finishing techniques were used. Plaque on these surfaces was compared with that on control surfaces with polished metallic or glazed porcelain restorations, and unrestored enamel surfaces. Composite surfaces were covered with plaque after 24 hours regardless of the finishing technique used. Plaque did not collect on adjacent control teeth to this degree until the third day, although the diffence remained statistically significant. Surface discrepancies on the polished composites were shown in scanning electron micrographs and with laboratory measurements.