Application of Photoactive Nanomaterials in Degradation of Pollutants

Photoactive nanomaterials have been receiving increasing attention due to their potential application in the light-driven degradation of water and gas-phase pollutants. However, to exploit the great potential of photoactive materials and access their properties requires fine-tuning of their size/shape-dependent chemical–physical properties, and on the ability to integrate them in photoreactors or to deposit them onto large surfaces. Therefore, the synthetic approach as well as post-synthesis manipulation could strongly affect the final photocatalytic properties of the nanomaterial. The aim of the present Special Issue is to report on the most recent progress towards the application of photoactive nanomaterials and nanomaterial-based coatings in pollutant degradation, paying particular attention to cases close to real application: scalable synthetic approaches to nanocatalysts, preparation of nanocatalyst-based coatings, degradation of real pollutants and bacterial inactivation, and application in building materials

Photo-thermal effects in gold nanorods/DNA complexes

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Photocatalytic TiO2-Based Nanostructured Materials for Microbial Inactivation

Pathogenic microorganisms can spread throughout the world population, as the currentCOVID-19 pandemic has dramatically demonstrated. In this scenario, a protection against pathogensand other microorganisms can come from the use of photoactive materials as antimicrobial agents ableto hinder, or at least limit, their spreading by means of photocatalytically assisted processes activatedby light—possibly sunlight—promoting the formation of reactive oxygen species (ROS) that can killmicroorganisms in different matrices such as water or different surfaces without affecting humanhealth. In this review, we focus the attention on TiO2nanoparticle-based antimicrobial materials,intending to provide an overview of the most promising synthetic techniques, toward possiblelarge-scale production, critically review the capability of such materials to promote pathogen (i.e.,bacteria, virus, and fungi) inactivation, and, finally, take a look at selected technological applications

Catalytic hydrogenation of waste-derived lipids: A route to producing sustainable drop-in biofuels by using Re/TiO2 catalysts

The urgent threat of climate change compels modern society to transition to alternative energy sources swiftly. The production of sustainable liquid biofuels capable of substituting fossil-derived fuels is a topic of great interest. This study explores the effectiveness of Re/TiO2 catalysts in producing drop-in biofuels from waste-derived feedstock. Specifically, four Re-based catalysts supported on different TiO2 materials, namely TiO2 P25, TiO2 FSP, TiO2 M, TiO2 COTIOX were synthesized using the wet impregnation method, characterized and tested in the hydrodeoxygenation reaction of fatty acids, to uncover fundamental insight into this process. These catalysts exhibited varying levels of effectiveness. Apart from Re/TiO2 COTIOX, which showed the lowest conversion of fatty acids (30 %), the other three catalysts allowed over 98 % conversion of fatty acids into hydrocarbons after 6 h reaction, at 35 bar of H2, under solvent-free conditions and without pre-reduction of the catalyst. Notably, Re/TiO2 P25 was the most effective, attaining this remarkable result at 300 °C. The remaining catalysts, Re/TiO2 FSP and Re/TiO2 M, required higher temperatures (350 °C) to achieve complete hydrogenation of fatty acids into hydrocarbons. These effective catalysts also demonstrated great recoverability, reusability, and robustness, successfully converting waste-derived lipids, such as grease recovered from urban sewage sludge and waste cooking oil, into hydrocarbons. These findings underscore Re/TiO2 as a promising robust catalyst for waste-derived lipids hydrogenation, enabling the efficient production of drop-in biofuels and paving the way for innovative solutions in the renewable energy landscape

Eudragit s100 entrapped liposome for curcumin delivery: Anti-oxidative effect in Caco-2 cells

Curcumin is a natural polyphenol with strong antioxidant activity. However, this molecule shows a very poor bioavailability, instability, and rapid metabolism in vivo. In this work curcumin was loaded in Eudragit-coated liposomes to create a gastroresistant carrier, able to protect its load from degradation and free it at the site of absorption in the colon region. Small unilamellar vesicles were prepared and coated with Eudragit by a pH-driven method. The physico-chemical properties of the prepared systems were assessed by light scattering, transmission electron microscopy, infrared spectroscopy, and differential scanning calorimetry. The uptake of vesicles by Caco-2 cells and the anti-oxidant activity in cells were evaluated. The produced vesicles showed dimensions of about forty nanometers that after covering with Eudragit resulted to have micrometric dimensions at acid pH. The experiments showed that at pH > 7.0 the polymeric coating dissolves, releasing the nanometric liposomes and allowing them to enter Caco-2 cells. Delivered curcumin loaded vesicles were then able to decrease significantly ROS levels as induced by H2O2 in Caco-2 cells. The proposed work showed the possibility of realizing effective gastroresistant curcumin liposome formulations for the delivery of antioxidant molecules to Caco-2 cells, potentially applicable to the treatment of pathological conditions related to intestinal oxidative stress. View Full-Tex

Lipid-based systems loaded with PbS nanocrystals: near infrared emitting trackable nanovectors

Hydrophobic PbS nanocrystals (NCs) emitting in the near infrared spectral region were encapsulated in the core of micelles and in the bilayer of liposomes, respectively, to form polyethylene glycol (PEG)-grafted phospholipids. The phospholipid-based functionalization process of PbS NCs required the replacement of the pristine capping ligand at the NC surface with thiol molecules. The procedures carried out for two systems, micelles and liposomes, using PEG-modified phospholipids were carefully monitored by optical, morphological and structural investigations. The hydrodynamic diameter and the colloidal stability of both micelles and liposomes loaded with PbS NCs were evaluated using Dynamic Light Scattering (DLS) and z-potential experiments, and both were satisfactorily stable in physiological media. The cytotoxicity of the resulting PbS NC-loaded nanovectors was assessed by the in vitro investigation on Saos-2 cells, indicating that the toxicity of the PbS NC loaded liposomes was lower than that of the micelles with the same NC cargo, which is reasonable due to the different overall composition of the two prepared nanocarriers. Finally, the cellular uptake in the Saos-2 cells of both the NC containing systems was evaluated by means of confocal microscopy studies by exploiting a visible fluorescent phospholipid and demonstrating the ability of both luminescent nanovectors to be internalized. The obtained results show the great potential of the prepared emitting nanoprobes for imaging applications in the second biological window

Nanostructured Photoelectrochemical Biosensing Platform for Cancer Biomarker Detection

The innovative photoelectrochemical properties of multifunctional nanomaterials are here investigated for the development of biosensing platforms for rapid and sensitive detection of a class of cancer biomarker candidates, known as microRNAs. Many different transducers have been proposed, so far, for microRNA detection. Recently, with the emergence of novel photoelectrochemically active species and new detection schemes, photoelectrochemistry has received increasing attention. Gold nanostructures have been, here, used to modify TiO2 electrodes. The surface of the nanostructured platform has been modified by nucleic acid capture probes (CPs). Biotinylated target miRNAs have been recognized by the specific CPs. The biosensing platform has been incubated with streptavidin alkaline phosphatase and exposed to a proper substrate. The product of the enzymatic reaction has been photoelectrochemically monitored. A compact and hand-held analytical device has been developed in order to have a final prototype in line with the concept of point of care testing. (C) 2017 The Authors. Published by Elsevier Ltd

Uniform TiO2/In2O3 surface films effective in bacterial inactivation under visible light

This study shows that the surface modification of TiO2 is an effective route to increase the TiO2 absorption in the visible region up to similar to 600 nm for photocatalytic applications. The In2O3 decorated TiO2 films on polyester obtained by reactive sputtering were shown to accelerate the Escherichia coli inactivation under actinic and simulated solar light. TiO2 sputtered films for 10 min inactivated bacteria within 300 min under actinic light. The inactivation time was reduced when using a TiO2 10 min-In2O3 10 s sample to 150 min when using actinic light and 90 min by simulated sunlight with 50 mW/cm(2) (one half of AM1). Thinner TiO2-In2O3 coatings led to faster bacterial inactivation compared to thicker TiO2-In2O3 layers due to the reverse diffusion of the generated charges. The increase in the optical absorption of the green coloured TiO2-In2O3 film was a function of the In2O3 loading as detected by diffuse reflectance spectroscopy (DRS). Evidence of the lack of TiO2 lattice doping by the sputtered In2O3 was found by X-ray diffraction spectroscopy (XRD). The deconvolution of TiO2 bands detected by X-ray photoelectron spectroscopy (XPS) revealed the existence of Ti4+/Ti3+ signals suggesting redox catalysis at the surface of the TiO2-In2O3. The photo-induced interfacial charge transfer (IFCT) between TiO2 and In2O3 can be accounted for by the band position potentials of both semiconductors. The faster kinetics of TiO2-In2O3 inducing E. coli inactivation with a higher quantum efficiency compared to TiO2 takes place in spite of the low intensity of the IFCT optical absorption bands >400 nm

Preparation of drug-loaded small unilamellar liposomes and evaluation of their potential for the treatment of chronic respiratory diseases

The aim of the present investigation was to evaluate the influence of liposome formulation on the ability of vesicles to penetrate a pathological mucus model obtained from COPD affected patients in order to assess the potential of such vesicles for the treatment of chronic respiratory diseases by inhalation. Therefore, Small Unilamellar Liposomes (PLAIN-LIPOSOMEs), Pluronic® F127- surface modified liposomes (PF-LIPOSOMEs) and PEG 2000PE-surface modified liposomes (PEG-LIPOSOMEs) were prepared using the micelle-to-vesicle transition (MVT) method and beclomethasone dipropionate (BDP) as model drug. The obtained liposomes showed diameters in the range of 40-65 nm, PDI values between 0.25-0.30 and surface electric charge essentially close to zero. The encapsulation efficiency was found to be dependent on the BDP/lipid ratio used and, furthermore, BDP-loaded liposomes were stable in size both at 37°C and at 4°C. All liposomes were not cytotoxic on H441 cell line as assessed by the MTT assay. The liposome uptake was evaluated through a cytofluorimetric assay that showed a non-significant reduction in the internalization of PEG-LIPOSOMEs as compared with PLAIN-LIPOSOMEs. The penetration studies of mucus from COPD patients showed that the PEG-LIPOSOMEs were the most mucuspenetrating vesicles after 27 hours. In addition, PEG- and PF-LIPOSOMEs did not cause any effect on bronchoalveolar lavage fluid proteins after aerosol administration in the mouse. The results highlight that PEG-LIPOSOMEs show the most interesting features in terms of penetration through the pathologic sputum, uptake by airway epithelial cells and safety profile