Interphotoreceptor Retinoid‐Binding Protein Protects Retinoids from Photodegradation

Retinol degrades rapidly in light into a variety of photoproducts. It is remarkable that visual cycle retinoids can evade photodegradation as they are exchanged between the photoreceptors, retinal pigment epithelium and Müller glia. Within the interphotoreceptor matrix, all‐trans retinol, 11‐cis retinol and retinal are bound by interphotoreceptor retinoid‐binding protein (IRBP). Apart from its role in retinoid trafficking and targeting, could IRBP have a photoprotective function? HPLC was used to evaluate the ability of IRBP to protect all‐trans and 11‐cis retinols from photodegradation when exposed to incandescent light (0 to 8842 μW cm^?2); time periods of 0–60 min, and bIRBP: retinol molar ratios of 1:1 to 1:5. bIRBP afforded a significant prevention of both all‐trans and 11‐cis retinol to rapid photodegradation. The effect was significant over the entire light intensity range tested, and extended to the bIRBP: retinol ratio 1:5. In view of the continual exposure of the retina to light, and the high oxidative stress in the outer retina, our results suggest IRBP may have an important protective role in the visual cycle by reducing photodegradation of all‐trans and 11‐cis retinols. This role of IRBP is particularly relevant in the high flux conditions of the cone visual cycle.     

Use of differential impurity induced spectra for the investigation of phonon dispersion relations

The use of differential impurity induced spectra for the investigation of elementary excitations in solids is discussed. It is shown theoretically that the differential spectra are expected to have peaks at energies corresponding to energies of the excitation at critical points of the pure crystal independent of the nature of the impurity used. As an example we present experimental results of the derivative of the intensity of Raman scattered light with respect to wavelength from Tl doped KBr crystals.     

Popcorn‐Shaped Magnetic Core–Plasmonic Shell Multifunctional Nanoparticles for the Targeted Magnetic Separation and Enrichment,Label‐Free SERS Imaging,and Photothermal Destruction of Multidrug‐Resistant Bacteria

Over the last few years, one of the most important and complex problems facing our society is treating infectious diseases caused by multidrug‐resistant bacteria (MDRB), by using current market‐existing antibiotics. Driven by this need, we report for the first time the development of the multifunctional popcorn‐shaped iron magnetic core–gold plasmonic shell nanotechnology‐driven approach for targeted magnetic separation and enrichment, label‐free surface‐enhanced Raman spectroscopy (SERS) detection, and the selective photothermal destruction of MDR Salmonella DT104. Due to the presence of the “lightning‐rod effect”, the core–shell popcorn‐shaped gold‐nanoparticle tips provided a huge field of SERS enhancement. The experimental data show that the M3038 antibody‐conjugated nanoparticles can be used for targeted separation and SERS imaging of MDR Salmonella DT104. A targeted photothermal‐lysis experiment, by using 670 nm light at 1.5 W cm^?2 for 10 min, results in selective and irreparable cellular‐damage to MDR Salmonella. We discuss the possible mechanism and operating principle for the targeted separation, label‐free SERS imaging, and photothermal destruction of MDRB by using the popcorn‐shaped magnetic/plasmonic nanotechnology.     

Fabrication and gas separation properties of polybenzimidazole (PBI)/nanoporous silicates hybrid membranes

Composites of polybenzimidazole (PBI) with proton-exchanged AMH-3 and swollen AMH-3 were prepared, characterized by electron microscopy and X-ray scattering and tested for hydrogen/carbon dioxide ideal selectivity. Proton-exchanged AMH-3 was prepared under mild conditions by the ion exchange of Sr and Na cations in the original AMH-3 using aqueous solution of dl-histidine. Swollen AMH-3 was prepared by sequential intercalation of dodecylamine following the ion exchange in the presence of dl-histidine. Both silicate materials were introduced into a continuous phase of PBI as a selective phase. Mixed matrix nanocomposite membranes, prepared under certain casting conditions, with only 3 wt% of swollen AMH-3 present substantial increase of hydrogen/carbon dioxide ideal selectivity at 35 °C, i.e., more than by a factor of 2 compared to pure PBI membranes (40 vs. 15). Similar ideal selectivity was observed using higher loadings (e.g., 14%) of proton-exchanged AMH-3 particles suggesting that transport of hydrogen is faster than carbon dioxide in AMH-3-derived silicates. However, the ideal selectivity of mixed matrix membranes approaches that of pure polymer as the operating temperature increases to 100 °C and 200 °C. The composite membranes with AMH-3-derived materials were compared with MCM-22/PBI membranes. Composite membranes incorporating MCM-22 plate-like crystals show no selectivity enhancements possibly due to the presence of larger pores in MCM-22.