Ultrasound assisted synthesis of Ag-decorated TiO2 active in visible light.

Titanium dioxide is the most popular photocatalyst to degrade organic pollutants in air, as well as in water. The principal drawback preventing its commercial application lies in its limited absorption of the visible light (400-700nm), while it is active under UV irradiation (≤387nm). Supporting noble metals in the form of nanoparticles on TiO2 increases its activity in the visible range. However, both the synthesis of noble metal nanoparticles and their deposition on TiO2 are multi-step processes that often require organic solvents. Here, we deposit Ag nanoparticles from AgNO3 on the surface of micrometric TiO2 with H2O as a solvent and under ultrasound irradiation at 30Wcm-2. Ultrasound increases the surface amount of Ag on TiO2 with heterogeneous size distribution of Ag nanoparticles, which are bigger and overlaid (1-20nm vs. 0.5-3nm) compared to the sample obtained in traditional conditions (TEM images). While this change in morphology had no effect on acetone photodegradation under UV light, the 5%, 10%, and 20% Ag-TiO2 degraded 17%, 20% and 24% acetone under visible light, respectively. The 10% by weight Ag-TiO2 sample obtained in absence of ultrasound only degraded 14% acetone in 6h, while the bare TiO2 was not active.

Zn- vs Bi-based oxides for o-toluidine photocatalytic treatment under solar light.

The photodegradation of the highly toxic o-toluidine pollutant was deeply investigated both under UV and solar irradiations by using three different semiconductors: pure ZnO, Bi-impregnated ZnO, and Bi2O3 nanopowders (synthesized by precipitating method). All the samples were deeply characterized on structural, morphological, surface, and optical points of view. The disappearance and the relative mineralization of o-toluidine molecules were followed by linear sweep voltammetry (LSV) and total organic carbon (TOC) determinations, respectively. Hence, correlations between their physico-chemical properties and the photocatalytic performances, passing from UV to solar light, were drawn and a hypothesis on the photodegradation mechanism has been proposed, on the basis of the HPLC/MS results. Bare Bi2O3 samples, due to the exploitation of both their visible light absorption and the negligible intermediates formation, resulted to be higher performing under solar irradiation than either pure or Bi-doped ZnO nanopowders. Graphical abstract.

3D Mass Spectrometry Imaging Reveals a Very Heterogeneous Drug Distribution in Tumors.

Mass Spectrometry Imaging (MSI) is a widespread technique used to qualitatively describe in two dimensions the distribution of endogenous or exogenous compounds within tissue sections. Absolute quantification of drugs using MSI is a recent challenge that just in the last years has started to be addressed. Starting from a two dimensional MSI protocol, we developed a three-dimensional pipeline to study drug penetration in tumors and to develop a new drug quantification method by MALDI MSI. Paclitaxel distribution and concentration in different tumors were measured in a 3D model of Malignant Pleural Mesothelioma (MPM), which is known to be a very heterogeneous neoplasm, highly resistant to different drugs. The 3D computational reconstruction allows an accurate description of tumor PTX penetration, adding information about the heterogeneity of tumor drug distribution due to the complex microenvironment. The use of an internal standard, homogenously sprayed on tissue slices, ensures quantitative results that are similar to those obtained using HPLC. The 3D model gives important information about the drug concentration in different tumor sub-volumes and shows that the great part of each tumor is not reached by the drug, suggesting the concept of pseudo-resistance as a further explanation for ineffective therapies and tumors relapse.

Hazardous o-toluidine mineralization by photocatalytic bismuth doped ZnO slurries.

Photocatalytic mineralization of o-toluidine in aqueous media under UV/solar irradiation was achieved by bare and bismuth doped zinc oxide nanoparticles. By adopting different analytical approaches a reaction mechanism is proposed, explaining the differences in photodetoxification performances.