COVID-19, as the cause of a global pandemic, has resulted in lockdowns all over the world since early 2020. Both theoretical and experimental efforts are being made to find an effective treatment to suppress the virus, constituting the forefront of current global safety concerns and a significant burden on global economies. The development of innovative materials able to prevent the transmission, spread, and entry of COVID-19 pathogens into the human body is currently in the spotlight. The synthesis of these materials is, therefore, gaining momentum, as methods providing nontoxic and environmentally friendly procedures are in high demand. Here, a highly virucidal material constructed from SiO2-Ag composite immobilized in a polymeric matrix (ethyl vinyl acetate) is presented. The experimental results indicated that the as-fabricated samples exhibited high antibacterial activity towards Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) as well as towards SARS-CoV-2. Based on the present results and radical scavenger experiments, we propose a possible mechanism to explain the enhancement of the biocidal activity. In the presence of O2 and H2O, the plasmon-assisted surface mechanism is the major reaction channel generating reactive oxygen species (ROS). We believe that the present strategy based on the plasmonic effect would be a significant contribution to the design and preparation of efficient biocidal materials. This fundamental research is a precedent for the design and application of adequate technology to the next-generation of antiviral surfaces to combat SARS-CoV-2.

Pro-oxidant effects of phenolic compounds are usually correlated to the one-electron redox potential of the phenoxyl radicals. Here we demonstrated that, besides their oxidizability, hydrophobicity can also be a decisive factor. We found that esterification of protocatechuic acid (P0) provoked a profound influence in its pro-oxidant capacity. The esters bearing alkyl chains containing two (P2), four (P4) and seven (P7) carbons, but not the acid precursor (P0), were able to exacerbate the oxidation of trolox, α-tocopherol and rifampicin. This effect was also dependent on the catechol moiety, since neither gallic acid nor butyl gallate showed any pro-oxidant effects. A comparison was also made with apocynin, which is well-characterized regarding its pro-oxidant properties. P7 was more efficient than apocynin regarding co-oxidation of trolox. However, P7 was not able to co-oxidize glutathione and NADH, which are targets of the apocynin radical. A correlation was found between pro-oxidant capacity and the stability of the radicals, as suggested by the intensity of the peak current in the differential pulse voltammetry experiments. In conclusion, taking into account that hydroquinone and related moieties are frequently found in biomolecules and quinone-based chemotherapeutics, our demonstration that esters of protocatechuic acid are specific and potent co-catalysts in their oxidations may be very relevant as a pathway to exacerbate redox cycling reactions, which are usually involved in their biological and pharmacological mechanisms of action.

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The excessive activation of neutrophils generates reactive oxygen species (ROS) and the secretion of primary granular enzymes, such as myeloperoxidase (MPO), which is implicated in numerous inflammatory diseases. The aim of this study was to evaluate chalcones as inhibitors of the chlorinating activity of MPO using in vitro and ex vivo assays. In addition to cytotoxic properties, the inhibition of respiratory burst, the scavenger capacity, and the oxidation potential were measured. 4'-Aminochalcone (1), 4'-amino-4- fluorochalcone (2), and 4'-amino-4-methylchalcone (3) exhibited potent inhibition of the chlorinating activity of MPO, as evaluated in a neutrophil system and a free cell system, to the following degree: (1) IC50 = 0.265 � 0.036 μmol L-1; (2) IC50 = 0.250 � 0.081 μmol L-1; and (3) IC50 = 0.250 � 0.012 μmol L-1. These values were similar to those for 5-fluorotryptamine (IC50 = 0.192 � 0.012 μmol L-1), a compound considered to be a potent MPO inhibitor. These aminochalcones were not toxic to neutrophils at concentrations below 100 μmol L- 1, as determined by the trypan blue exclusion assay. Compounds 1-3 presented a high oxidation potential (Epa1 ≉ 0.80 V), low scavenger capacity against DPPH• and HOCl, and low inhibition of respiratory burst. These data indicated that aminochalcones are potent inhibitors of MPO chlorinating activity, a new property for chalcone derivatives, given that they are neither antioxidant agents nor inhibitors of respiratory burst. In conclusion, the selected aminochalcones have potential as pharmacological agents for inflammatory diseases.

The ongoing COVID-19 pandemic has pushed scientists and technologists to find novel strategies to develop new materials to prevent the transmission, spread, and entry of pathogens into the human body. In this report, the fabrication of polyvinyl chloride (PVC)-SiO 2 -Ag composite is presented, in which the percentage of Ag is 0.84% wt. Our findings render that this composite eliminates (> 99.8%) bacteria and fungus ( Staphylococcus aureus , Escherichia coli , Penicillium funiculosum ) and SARS-CoV-2, by surface contact in 2 h hours and 15 min, respectively. Specific migration analysis shown that the use of the PVC-SiO 2 -Ag composite is considered safe and effective for food preservation. This research and innovation front can be considered a breakthrough for the design of biocide materials. Future directions for this exciting and highly significant research field can open the door to the development of new technologies for the fabrication of packaging films to protect consumer products (such as fruits, vegetables, and other foods). Supplementary information The online version contains supplementary material available at 10.1007/s10965-021-02729-1.

Fx1 Highlights: • Thin alumina barrier coating can enhance photo-activity of bismuth vanadate photoanode materials • There are two distinct potential domains with different enhancement characteristics and mechanisms • The thickness of alumina films can be controlled with a sol-gel coating to provide optimized performance Abstract Nanostructured semiconductor photoanodes play an important role in solar fuel generation, and the design of the semiconductor -aqueous electrolyte interface can be crucial in enhancing the energy conversion efficiency. We have investigated the effects on photoelectrochemical oxygen evolution for monoclinic nanostructured BiVO4 films uncoated and coated with microporous sol-gel Al2O3 "over-layers". Variation of the thickness of the Al2O3 coating (formed by surface sol-gel deposition and annealing at 435 o C) led to a reduction of pseudo-capacitance and allowed optimization of the quantum efficiency. Exploration of the photocurrent enhancement as a function of applied potential reveals two distinct potential domains/mechanisms: (i) a low bias region enhancement effect (assigned to a lowering of the rate of external recombination of electrons with oxygen) and (ii) a high bias region of enhancement (assigned to higher charge carrier mobility due to less trapping in surface states).

In this paper, we study theoretically and experimentally the effect of induced charging currents on the fast-scan cyclic voltammetry. As explained in this paper, the phenomenon originates from the coupling between faradaic and capacitive currents in the presence of uncompensated resistance. Due to the existence of induced charging currents, the capacitive contribution to the total current is different from the capacitive current measured in the absence of electroactive species. In this paper, we show that this effect is particularly important when the ratio of the capacitive current and the total current is close to unity, even for a relatively low cell time constant. Consequently, the conventional background subtraction method may be inaccurate in these situations. In this work, we develop a method that separates the faradaic and capacitive currents, combining simulation and experimental data. The method is applicable even in the presence of potential-dependent capacitance. The theoretical results are compared with some previously reported results and with experiments carried out on the potassium ferrocyanide/ferricyanide redox couple. Platinum disk electrodes of different diameters and NaClO4 support electrolyte of different concentrations were used to obtain different cell time constants. The proposed method allowed us to separate the real capacitive current even in the situations where the conventional background subtraction used in many published papers is clearly inappropriate.

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