Engineering DNA-Grafted Quatsomes as Stable Nucleic Acid-Responsive Fluorescent Nanovesicles

The development of artificial vesicles into responsive architectures capable of sensing the biological environment and simultaneously signaling the presence of a specific target molecule is a key challenge in a range of biomedical applications from drug delivery to diagnostic tools. Herein, the rational design of biomimetic DNA-grafted quatsome (QS) nanovesicles capable of translating the binding of a target molecule to amphiphilic DNA probes into an optical output is presented. QSs are synthetic lipid-based nanovesicles able to confine multiple organic dyes at the nanoscale, resulting in ultra-bright soft materials with attractiveness for sensing applications. Dye-loaded QS nanovesicles of different composition and surface charge are grafted with fluorescent amphiphilic nucleic acid-based probes to produce programmable FRET-active nanovesicles that operate as highly sensitive signal transducers. The photophysical properties of the DNA-grafted nanovesicles are characterized and the highly selective, ratiometric detection of clinically relevant microRNAs with sensitivity in the low nanomolar range are demonstrated. The potential applications of responsive QS nanovesicles for biosensing applications but also as functional nanodevices for targeted biomedical applications is envisaged.     

Calculation of pure saturation properties using cubic equations of state

A robust algorithm is outlined for the solution of the classical non-linear isofugacity problem by using equations of state (EOS). The procedure suggested is free of numerical pitfalls from the triple point to the critical point. The combination of differential stability (spinodal curve) and zero pressure reference concepts yields an automatic initialization of the calculations inside a region of convergence where the EOS can always predict pure compound vapor pressures at a given temperature.     

Imidacloprid oxidation by photo-Fenton reaction

This paper presents experimental results on the imidacloprid removal from wastewater using homogeneous photo-Fenton reactions illuminated with black light lamps. Multivariate experimental design was used to identify the effect of initial Fe(II) and H₂O₂ concentrations on process performance. The initial iron concentration played a key role in the process kinetics, whereas hydrogen peroxide concentration directly affected the extent of the oxidation process.

Imidacloprid degradation proceeded via two distinctive kinetics regimes, an initial stage of rapid imidacloprid reduction, followed by a slower oxidation process until complete removal. Under optimal conditions, more than 50% imidacloprid degradation was observed after less than 1 min treatment, and TOC and COD removal up to 65% and 80%, respectively, were measured after all hydrogen peroxide was consumed.

Raw imidacloprid samples presented significant acute toxicity to Daphnia magna and genotoxic effects on Bacillus subtilis sp. Such toxic effects remained detectable even after significant pesticide removal had been achieved, due to the presence of toxic by-products. Both acute toxicity and genotoxicity disappeared after considerable mineralization resulting in final low molecular weight by-products. Results obtained here confirm that design and operation of photo-Fenton processes should focus on toxicity removal rather than on specific target pollutants.     

Diode-pumped 2 μm vibronic (Tm3+, Yb3+):KLu(WO4)2 laser

We report on laser operation in a (6 at. % Tm, 5 at. % Yb):KLu(WO4)2 codoped crystal. The vibrational frequencies of KLu(WO4)2 are coupled to the electronic transitions of Tm3+ at 1946 nm, creating virtual final laser levels at higher energy than the ground level 3H6 of Tm3+. The longest recorded laser wavelength was 2039 nm, which is longer than permitted by a pure electronic transition in Tm3+ ions in KLu(WO4)2. We show that every laser wavelength can be explained with the electron-phonon coupling effect, where the vibration frequencies were determined through Raman spectroscopy.     

A high-flexibility DC load for fuel cell and solar arrays power sources based on DC–DC converters

In this paper, a flexible DC load to test and evaluate current–voltage characteristics of fuel cells stacks and photovoltaic modules based on DC–DC converters is proposed. The load features are simple structure, scalability, low cost, and its possibility to emulate an arbitrary load profile. The measure of the desired characteristics of fuel cells and photovoltaic modules further includes high speed of response and high fidelity. A comparison between conventional methods and the proposed one is also provided. Experimental results show the usefulness of the DC load proposed.     

Electronic structure of p-type ultraviolet-transparent conducting CuScO2 films

We investigate the electronic structure of CuScO₂ thin films grown on sapphire and mica substrates by pulsed laser deposition. X-ray diffraction and microanalysis confirm that the films have the expected delafossite crystal structure and stoichiometric proportions. The electronic structure is investigated by means of X-ray and ultraviolet photoelectron spectroscopy. Electronic states in the range 0-1350 eV are identified, making reference to theoretical density-of-states calculations up to 80 eV. Photoelectron spectra near the Fermi energy confirm the p-character of the films. Optical absorption spectroscopy shows that the films are transparent up to 3.7 eV and exhibit an intense excitonic peak, with a direct gap energy of 4.24 ± 0.05 eV at room temperature. Ab initio band structure calculations confirm the direct character of CuScO₂ and allow for an assignment of the direct gap to an electronic transition at the L point of the rhombohedral Brillouin zone.     

Coupling of a microfluidic mixer to a Fourier-transform infrared spectrometer for protein-conformation studies

The biological properties of a protein critically depend on its conformation, which can vary as a result of changes in conditions such as pH or following the addition of various substances. Being able to reliably assess the quality of protein structures under various conditions is therefore of crucial importance. Infrared (IR) spectroscopy of the Amide I band of proteins is a powerful method for the determination of protein conformations and further allows the analysis of continuously flowing solutions of the target molecule. Here, a commercial Fourier-transform infrared spectrometer was coupled to a microfluidic mixer to allow the on-line monitoring of protein conformation under varying conditions. The validity of the concept was demonstrated by continuously recording the variations of the IR spectrum of poly-L-lysine resulting from repetitive, pH-induced conformational changes.