Tunable Assembly of Photocatalytic Colloidal Coatings for Antibacterial Applications.

In this study, evaporation-induced size segregation and interparticle interactions are harnessed to tune the microstructure of photocatalytic colloidal coatings containing TiO nanoparticles and polymer particles. This enabled the fabrication of a library of five distinct microstructures: TiO-on-top stratification, a thin top layer of polymer or TiO, homogeneous films of raspberry particles, and a sandwich structure. The photocatalytic and antibacterial activities of the coatings were evaluated by testing the viability of Methicillin-resistant (MRSA) bacteria using the ISO-27447 protocol, showing a strong correlation with the microstructure.

Self-Assembly of Soluplus in Aqueous Solutions: Characterization and Prospectives on Perfume Encapsulation.

Soluplus is an amphiphilic graft copolymer intensively studied as a micellar solubilizer for drugs. An extensive characterization of the nanostructure of its colloidal aggregates is still lacking. Here, we provide insights into the polymer's self-assembly in water, and we assess its use as an encapsulating agent for fragrances.

Physicochemical characterization of green sodium oleate-based formulations. Part 2. Effect of anions.

Hypothesis: In Part 1 of this work we reported the behavior of a moderately concentrated dispersion of sodium oleate (NaOL) in water that produces elongated wormlike micelles (WLMs). Prompted by the striking effect induced by adding potassium chloride to the original NaOL dispersion, here we investigate the effect of different anions (with fixed cation) on NaOL or KOL-based hydrogels upon addition of different strong electrolytes. The interest in these investigations relies on the fact that they are among the best candidates for the production of eco-friendly stimulus-responsive materials.

Encapsulation of volatile compounds in liquid media: Fragrances, flavors, and essential oils in commercial formulations.

The first marketed example of the application of microcapsules dates back to 1957. Since then, microencapsulation techniques and knowledge have progressed in a plethora of technological fields, and efforts have been directed toward the design of progressively more efficient carriers. The protection of payloads from the exposure to unfavorable environments indeed grants enhanced efficacy, safety, and stability of encapsulated species while allowing for a fine tuning of their release profile and longer lasting beneficial effects.

Tuning the Encapsulation of Simple Fragrances with an Amphiphilic Graft Copolymer.

The encapsulation of poorly water-soluble compounds such as perfumes, flavors, and bioactive molecules is a key step in the formulation of a large variety of consumer products in the fields of household care and personal care. We study the encapsulation ability of an amphiphilic poly(ethylene glycol)--poly(vinyl acetate) (PEG--PVAc) graft copolymer, extending the focus to the entire phase diagram of polymer/perfume/water systems with three common natural fragrances. The three perfume molecules (2-phenyl ethanol, L-carvone, and α-pinene) possess different water affinities, as expressed by their octanol/water partition coefficients.

Binding of lanthanide salts to zwitterionic phospholipid micelles.

As the use of lanthanide salts in biophysical systems increases and the separation of lanthanides from nuclear and other wastes with extraction processes has become an important technological challenge, a deeper understanding of the behavior of lanthanides at lipid interfaces is urgently needed. In this work the interaction of lanthanide salts with zwitterionic phospholipids is probed using aqueous micelles of the surfactant dodecyl phosphocholine (DPC), which are useful membrane-mimetic model systems, widely used for the solubilization of membrane proteins in aqueous solutions. Because more than one species exists in lanthanide salt solutions, even at the pH value of 4 used in this experiment, the major goal of this investigation is to examine which species are actually binding to the micelles.