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.     

Solid acid (superacid) catalyzed regioselective adamantylation of substituted benzenes

Adamantylation of substituted benzenes with 1-bromo-adamantane was catalyzed by solid acids including acidic ion exchange and ionomer resins, HY zeolite, sulfated zirconia and supported superacids on HY zeolite and SiO₂. Adamantylation generally takes place in excellent yield giving predominantly para products without formation of byproducts. The reactions did not require the usual workup of Friedel-Crafts reactions as catalysts were simply filtered of. Cross-linked polystyrene resin sulfonic acid (Amberlyst) was found particularly suitable as besides its high catalytic activity, high regioselectivity was observed with almost exclusive formation ofp-adamantylated benzenes. AMI, PM3 and MNDO semiempirical calculations of heats of formation showed that of all regioisomers, the para isomer is the most stable. The temperature dependence of adamantylation was also investigated allowing the optimization ofp-substituted product in high yield and excellent selectivity. Lack of isomerization of 1-p-tolyla-damantane using solid (Amberlyst, Nafion-H) and liquid acids (neat and modified trifluoromethanesulfonic acid) indicates absence of product isomerization, while the intramolecular rearrangement of the intermediate arenium complex is still possible.Catalysis by solid superacids, Part 30. For part 29, see ref.[1A].     

Antibacterial LDPE Nanocomposites Based on Zinc Oxide Nanoparticles/Vermiculite Nanofiller

Polyethylene (PE) nanocomposites with the zinc oxide-nanoparticles/vermiculite nanofiller were prepared in two-steps. In first step, the ZnO-np/V nanofiller were prepared by the mechanochemical method followed by a heat treatment at 650?°C for 90 min. In second step, this nanofiller was used in concentration 3, 6, 10 and 15 wt% for PE nanocomposites preparation via melt compounding technique, the nanocomposites plates were pressed. The particles morphology of the ZnO-np/V nanofiller, arrangement of the ZnO-np/V nanofiller and surface of the PE plates were studied using scanning electron microscopy, optical light microscopy and atomic force microscopy. The surface roughness of the PE plates was evaluated from AFM measurements. Structural changes of the ZnO-np/V nanofiller in PE nanocomposites were monitored using X-ray diffraction analysis and Fourier transform infrared analysis. The gradual and long-term antibacterial effect of PE nanocomposites was tested on the Gram positive bacteria E. faecalis by counting the colony forming units number.     

Topologically controlled growth of magnetic-metal-functionalized semiconductor oxide nanorods

Colloidal semiconductor-magnetic hybrid nanocrystals with topologically controlled composition are fabricated by heterogeneous nucleation of spherical epsilon-Co domains onto anatase TiO2 nanorods. The latter can be selectively decorated at either their tips or at multiple locations along their longitudinal sidewalls, forming lattice-matched heterointerfaces regardless of the metal deposition sites. The possibility of switching between either heterostructure growth modes arises from the facet-dependent chemical reactivity of the oxide seeds, which is governed mainly by selective adhesion of the surfactants rather than by small differences in misfit-induced interfacial strain at the relevant junction points.     

Polyblend fibers from polypropylene and mercapto-modified EVA

Polyblend fibers were made from mixtures of polypropylene (PP) and ethylene-vinyl acetate copolymers (EVA) or their mercapto-modified products [poly(ethylene-co-vinyl acetate-co-vinyl mercaptoacetate)] (EVASH). The presence of few EVA or EVASH in the PP fibers results in an increasing of the elastic modulus, indicating a reinforcing action of these functional polymers. The composition surface of the modified PP fibers was analyzed by X-ray photoelectron spectroscopy and diffuse reflectance infrared Fourier transform spectroscopy. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 2243–2249, 1997     

The effect of hydroxyl‐terminated polybutadiene‐grafted carbon fiber on the impact performance of carbon fiber–epoxy resin composites

Carbon fiber (CF) containing 1.4 and 2.1 mmol/g of —COOH and —OH groups, respectively, was functionalized by using an excess of tolylene‐2,4‐diisocyanate. The NCO‐modified CF was submitted to a graft reaction with hydroxyl‐terminated polybutadiene (HTPB). The HTPB‐grafted carbon fiber was employed as reinforcing agent for epoxy resin‐based composites. The presence of the flexible HTPB at the interface between the fiber and the matrix resulted in a substantial improvement on impact strength. Additional improvement on toughness was achieved by using epoxy matrix containing dispersed phase of HTPB. The composite morphology was also studied by scanning electron microscopy. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1424–1431, 1999     

Evaluating and comparing three community small-scale wind electrification projects

Electrification systems based on renewable energy have proven suitable for providing electricity autonomously to rural communities. Among the technical options available, wind systems are increasingly getting attention. In the northern mountains of Peru, at 3800 m.a.s.l., three community wind electrification projects have been implemented. The technical solutions used in each project are different: wind vs. hybrid photovoltaic-wind systems; individual equipment vs. microgrids. This study aims to describe, evaluate and compare these three small-scale community wind electrification projects. The evaluation of the three projects was carried out by comparing previous and present scenario; attention has been focused on project design and technical aspects, socio-economic impacts and sustainability and management model. These three examples shed light on both the advantages and disadvantages of different technological options as well as on appropriate community-level management models.     

Effect of branched PP content on the physical properties and cell growth during foaming of TPOs

Linear/branched PP blends at various ratios were used as the matrix for thermoplastic olefin (TPO) compounds, containing an ethylene–octene copolymer dispersed phase. A detailed investigation of the physical properties of these blends revealed that addition of branched PP (BPP) resulted in improved stiffness and flexural properties. Given that the phase morphology of the blends and the interfacial tension between their components remained virtually unaffected, these improvements are attributed to the higher stiffness of the BPP‐containing matrices. Talc‐filled TPOs containing branched PPs exhibited further improvements in the stiffness and flexural properties. An investigation into the bubble growth process during foaming using a batch foaming simulation system revealed that the presence of BPP resulted in a slight delay in cell nucleation, whereas the rate of bubble growth was not significantly altered. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Novel spectropolarimeter employing fixed polarizers for the determination of optically active samples

A novel spectropolarimeter, based on modification of an ordinary, inexpensive, multiwavelength ultraviolet (UV)-visible-near-infrared (NIR) spectrophotometer, is described and applied to the determination of sucrose, sucrose inversion, and enantiomeric composition of solutions of (R)-(+)-limonene and (S)-(-)-limonene. The instrument has no moving parts, and optical rotation measurements are encoded as an apparent absorbance. Apparent absorbance measurements can be combined with multivariate statistical analysis over a wide spectral range, and a background correction technique that employs the sample as its own blank provides an effective means of correcting for the presence of chromophores that also absorb over the wavelengths of interest. The instrument was tested against an ordinary polarimeter and showed good performance with both colorless and colored samples.