Highly effective antimicrobial agents are needed to control the emergence of new bacterial strains, their increased proliferation capability, and antibacterial resistance that severely impact public health, and several industries including water, food, textiles, and oil and gas. Recently, bimetallic nanoparticles, formed via integration of two different metals, have appeared particularly promising with antibacterial efficiencies surpassing that of monometallic counterparts due to synergistic effects, broad range of physiochemical properties, and diverse mechanisms of action. This work aims to provide a review on developed bimetallic and supported bimetallic systems emphasizing in particular on the relation between synthesis routes, properties, and resulting efficiency. Bimetallic nanostructures on graphene, zeolites, clays, fibers, polymers, as well as non-supported bimetallic nanoparticles are reviewed, their synthesis methods and resulting properties are illustrated, along with their antimicrobial activity and potential against different strains of microbes.
Here, we demonstrate the synthesis of mesoporous carbon dots (Cdot) from date palm fronds and their excellent excitation wavelength-independent photoluminescence (PL), with high photo- and storage-stability, superior biocompatibility and thermal and electrical conductivity for the first-time by a simple, green, one-step carbonization method. Interestingly, the as-obtained Cdot manifest the spherical shape of about 50 nm average diameter having surface mesopores of size less than 10 nm with sp2 hybridized carbon. The as-synthesised mesoporous Cdot, first of its kind, evince yellow-green PL (preferred over blue PL for biological applications) around 450 nm under excitation wavelength range of 320–420 nm with absolute quantum yield of 33.7% exhibiting high photo- and storage-stability. The thermal and electrical conductivity of Cdot/water nanofluids without any surfactants is illustrated. Application of Cdot as interfacial material in organic photovoltaic cell is manifested. The Cdot exhib visible sunlight driven photocatalytic and antibacterial activity. Mesoporous Cdot further reveal excellent biocompatibility with fibroblast cell (greater than 95% viability). The novelty of this study in the formation of multifunctional mesoporous Cdot from date palm fronds could inspire both research and industrial interests in the synthesis of biomass-derived Cdot and their application in a wide array of fields.
Graphene oxide (GO) was functionalized covalently with pH-sensitive poly(2-(diethylamino) ethyl methacrylate) (PDEA) by surface-initiated in situ atom transfer radical polymerization. The structure of the PDEA-grafted GO (GO-PDEA) were examined by Fourier-transform infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis and atomic force microscopy. The grafted PDEA endowed the GO sheets with good solubility and stability in physiological solutions. Simple physisorption by π-π stacking and hydrophobic interactions on GO-PDEA can be used to load camptothecin (CPT), a widely used water-insoluble cancer drug. The loaded CPT was released only at the lower (acidic) pH normally found in a tumor environment but not in basic and neutral pH. GO-PDEA did not show practical toxicity to N2a cancer cells but the GO-PDEA-CPT complex exhibited high potency in killing N2a cancer cells in vitro. These results suggest that the GO-PDEA nanocargo carrier might be a promising material for site-specific anticancer drug delivery and controlled release.
A pH-sensitive poly(acrylic acid)-grafted graphene oxide (GO-PAA) nanocarrier was synthesized by in situ atom transfer radical polymerization to allow the oral delivery of hydrophilic macromolecular proteins in their active forms to specific cells or organs. The synthesis, morphology, and physiochemical properties of GO-PAA were examined. A model protein, bovine serum albumin (BSA) labeled with fluorescein isothiocyanate (FITC) (BSAFITC), was loaded onto GO-PAA through noncovalent interactions and its release was arrested at acidic pH similar to stomach, whereas at pH similar to intestine it was reduced, which paves way for site specific delivery without its degradation in the gastrointestinal tract. Confocal laser microscopy showed that the BSAFITC-loaded GO-PAA was internalized by KB cells by endocytosis and released into cytoplasm. Thus the GO-PAA as a transmembrane transporter is a new class of drug transporters with potential protein delivery applications.
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