64 research outputs found
LYSOZYME INTERACTION WITH NEGATIVELY CHARGED LIPID BILAYERS: PROTEIN AGGREGATION AND MEMBRANE FUSION
Understanding the effects of Cr doping in rutile TiOâ‚‚ by DFT calculations and X-ray spectroscopy
The effects of Cr on local environment and electronic structure of rutile TiOâ‚‚ are studied combining theoretical and experimental approaches. Neutral and negatively charged substitutional Cr impurities Cr_(Ti)(0)* and Cr_(Ti)(-1)* as well as Cr-oxygen vacancy complex 2Cr_(Ti) + Vâ‚€ are studied by the density functional theory (DFT) within the generalized gradient approximation (GGA) of Perdew-Burke-Ernzerhof (PBE) functional. Experimental results based on X-Ray absorption spectroscopy (XAS) and X-Ray photoelectron spectroscopy (XPS) performed on Cr doped TiOâ‚‚ at the Synchrotron facility were compared to the theoretical results. It is shown that the electrons of the oxygen vacancy tend to be localized at the t_(2g) states of the Cr ions in order to reach the stable oxidation state of Cr(3+)*. Effects of Cr on crystal field (CF) and structural distortions in the rutile TiOâ‚‚ cell were analyzed by the DFT calculations and XAS spectra revealing that the CF and tetragonal distortions in TiOâ‚‚ are very sensitive to the concentration of Cr
Glucose is a key driver for GLUT1-mediated nanoparticles internalization in breast cancer cells
The mesenchymal state in cancer is usually associated with poor prognosis due to the metastatic predisposition and the hyper-activated metabolism. Exploiting cell glucose metabolism we propose a new method to detect mesenchymal-like cancer cells. We demonstrate that the uptake of glucose-coated magnetic nanoparticles (MNPs) by mesenchymal-like cells remains constant when the glucose in the medium is increased from low (5.5 mM) to high (25 mM) concentration, while the MNPs uptake by epithelial-like cells is significantly reduced. These findings reveal that the glucose-shell of MNPs plays a major role in recognition of cells with high-metabolic activity. By selectively blocking the glucose transporter 1 channels we showed its involvement in the internalization process of glucose-coated MNPs. Our results suggest that glucose-coated MNPs can be used for metabolic-based assays aimed at detecting cancer cells and that can be used to selectively target cancer cells taking advantage, for instance, of the magnetic-thermotherapy
THYROID STIMULATING HORMONE AND THYROXINE SCREENING IN THE PRETERM NEWBORN: REFERENCE VALUES
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Study of the interaction mechanism between hydrophilic thiol capped gold nanoparticles and melamine in aqueous medium
In the last years, intense efforts have been made in order to obtain colloidal-based systems capable of pointing out the presence of melamine in food samples. In this work, we reported about the recognition of melamine in aqueous solution, using gold nanoparticles stabilized with 3-mercapto-1-propanesulfonate (AuNPs-3MPS), with the aim of deepening how the recognition process works. AuNPs were synthesized using a wet chemical reduction method. The synthesized AuNPs-3MPS probe was fully characterized, before and after the recognition process, by both physicochemical (UV–vis, FT-IR, 1H-NMR, DLS and ζ-potential) and morphostructural techniques (AFM, HR-TEM). The chemical and electronic structure was also investigated by SR-XPS. The sensing method is based on the melamine-induced aggregation of AuNPs; the presence of melamine was successfully detected in the range of 2.5−500 ppm. The results achieved also demonstrate that negatively charged AuNPs-3MPS are potentially useful for determining melamine contents in aqueous solution. SR-XPS measurements allowed to understand interaction mechanism between the probe and the analyte. The presence of sulfonate groups allows a mutual interaction mediated by electrostatic bonds between nanoparticles surface thiols and positively charged amino groups of melamine molecules
SCREENING TEST FOR CONGENITAL HYPOTHYROIDISM: THYROID STIMULATING HORMONE (TSH) AND THYROXINE (T4) IN THE ADAPTED FOR GESTATIONAL AGE NEWBORN (AGA) AND IN THE SMALL FOR GESTATIONAL AGE NEWBORN (SGA) AT TERM AND PRETERM
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