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Regulation of wound pH from alkaline to acidic is a simple and powerful approach to reduce wound microbial colonization and infection. Here, we present a nanocomposite material possessing intrinsic acidic surface pH as an innovative antimicrobial wound dressing. This material comprises an agarose matrix nanocomposite containing nanoparticles (NPs) of the cesium salt of phosphotungstic heteropolyacid (Cs 2.5 H 0.5 PW 12 O 40 ). Self-supporting films were prepared by a casting method incorporating 5-20 wt % Cs 2.5 H 0.5 PW 12 O 40 NPs into the matrix. Films are flexible with tensile strengths between 28.55 and 32.15 MPa and exhibit broad biocidal activity against neutralophilic pathogens, including Gram-positive bacteria, Gram-negative bacteria, yeast, and filamentous fungi. The nano-antimicrobial Cs 2.5 H 0.5 PW 12 O 40 functions as an efficient and self-controlled proton delivery agent that lowers the surface pH of the nanocomposites to the range 7.0 > pH ≥ 3.0. Nanocomposite films containing 20 wt % Cs 2.5 H 0.5 PW 12 O 40 NPs presented a surface pH of 3.0 and highest antimicrobial activity. Using quantitative reverse transcription polymerase chain reaction, we demonstrated that the antimicrobial mechanism of the nanocomposites is acid-induced because of the transcriptional induction of glutamate-dependent acid resistance genes in Escherichia coli. Additionally, nanocomposite films do not damage skin according to an in vivo rabbit skin model with no derived edema or erythema. The wound care safety of this material is due to low release of heavy metal heteropolyanions ([PW 12 O 40 ] 3- ), no nanoparticle leaching, and proton controlled release resulting in nonirritating acid levels for human skin models.

The transfer of pathogens from contaminated surfaces to patients is one of the main causes of health care-associated infections (HCAIs). Cases of HCAIs due to multidrug-resistant organisms have been growing worldwide, whereas inorganic nano-antimicrobials are valuable today for the prevention and control of HCAIs. Here, we present a cesium salt of phosphotungstic heteropolyacid (Cs 2.5 H 0.5 PW 12 O 40 ) as a promising nanomaterial for use in antimicrobial product technologies. This water-insoluble Keggin salt exhibits a broad biocide spectrum against Gram-positive and Gram-negative bacteria, yeasts, and filamentous fungi even under dark conditions. The Cs 2.5 H 0.5 PW 12 O 40 nanoparticles (NPs) act as a proton-regulated antimicrobial whose activity is mediated on the release of hydronium ions (H 3 O + ), yielding an in situ acidic pH several units below those tolerable by most of the fungal and bacterial nosocomial pathogens.

The purpose of this study is to evaluate the efficacy of yttria-stabilized zirconia (3Y-TZP) as an inert phase to prevent the decomposition of Bi2 V0.9 Cu0.1 O5.5 -δ (BICUVOX.1) electrolyte under reducing atmosphere. A post-mortem scanning electron microscopy (SEM) study was performed after chemical stability tests under hydrogen-rich atmosphere using a Sieverts-type apparatus. SEM results showed that BICUVOX.1 decomposition starts under a hydrogen pressure of 19.7 atm at 300°C, even in the case of the composite containing 3Y-TZP. The microstructure of BICUVOX.1 after decomposition was observed to be composed of microspheres ranging from 10 to 100 µm formed primarily of metallic bismuth. In the composite, in addition to microspheres, the microstructure contained bismuth fibers growth from the grain area of the BICUVOX.1 matrix. Despite significant surface morphological modifications, the grain-boundary-arranged 3Y-TZP particles in a BICUVOX.1-matrix composite did not result in enhanced chemical stability., (© Wiley Periodicals, Inc.)