Cationic poly(lactide-co-glycolide) nanoparticles as efficient in vivo gene transfection agents

Poly(lactide-co-glycolide) (PLGA), a biocompatible and biodegradable polyester co-polymer of PLA and PGA, has been recognized for its ability to deliver genes. However, gene delivery by PLGA nanoparticles is limited by their negative charge and their poor transport through mucosal barriers. In this study, PLGA nanoparticles were surface modified with cationic chitosan in an effort to improve their gene delivery capability. PLGA nanoparticles were synthesized by emulsion-diffusion-evaporation technique using PVA-chitosan (PLGA1) or PVA-chitosan-PEG (PLGA2) blend as stabilizers. This method is reproducible and produces nanoparticles with hydrodynamic diameter <200 nm. The nanoparticles were characterized by zetasizer, photon correlation spectroscopy and atomic force microscopy. A549 epithelial cells were transfected in vitro with PLGA particles complexed with a reporter plasmid encoding green fluorescent protein. PLGA particles transferred EGFP gene, but were less efficient than the lipofectamine control. The nanoparticles were also tested for their ability to transport across the nasal mucosa in vivo in mice. The results show that both PLGA1 and PLGA2 facilitate gene delivery and expression in vivo with increased efficiency and without causing inflammation, as measured by IL-6. Together, these results indicate that chitosan-modified PLGA nanoparticles have greater potential as gene carriers.     

The Number of Neighbors Needed for Connectivity of Wireless Networks

Wireless Networks - Unlike wired networks, wireless networks do not come with links. Rather, links have to be fashioned out of the ether by nodes choosing neighbors to connect to. Moreover the...     

Vapour phase crystal growth under microgravity environment

Vapour phase crystal growth experiments performed in the Skylab and ASTP missions are reviewed. The basic vapour phase crystal growth technique is described and effect of gravity is discussed. The multipurpose furnace specially designed to carry out various experiments in flight conditions is described. Ge Se, Ge Te and GeS as well as ternary GeSe_0·99 Te_0·01 and GeS_0·98 Se_0·02 crystals have been grown in space showing improvement over similarly grown crystals on ground as determined by x-ray diffraction, chomical homogeneity and surface morphology studies. Mass flux rates under microgravity conditions have been found to be up to 10 times larger than expected indicating need for better theoretical and experimental understanding of the effect of gravity on crystal growth.     

Statistical separability of spectral classes of blighted corn

The purpose of this study was to determine the statistical separability of multispectral measurements from corn having varying levels of southern corn leaf blight severity. Multispectral scanner data in twelve spectral channels in the wavelength range 0.4 to 11.7 μm were analyzed for ten selected flightlines of the 1971 Corn Blight Watch Experiment. A total of 168 corn fields having 18,804 sample points were analyzed. The blight rating information for these fields was available from ground observations. Maximum average transformed divergence between spectral classes (found by LARSYS Cluster Algorithm) of all possible pairs of blight levels, maximized over a subset of channels, was computed in each of one, two, three, and four spectral channels for each of ten flightlines. From the statistical analysis of the values of average transformed divergence, it was concluded that the greater the difference between the blight levels, the more statistically separable they are. This result is encouraging considering the fact that there are variables other than the blight severity within and between the flightlines. Although the analysis was done for corn blight only, the conclusions obtained from this analysis may well be applicable to other crop stresses because corn blight is representative of many plant stresses, especially non-systemic stresses.     

Flow injection analysis of an ultratrace amount of arsenite using a Prussian blue-modified screen-printed electrode

We report here a new electrochemical method for the selective detection of ultratrace amount of arsenite (AsO(2)(-), As(3+)) using a Prussian blue-modified screen-printed electrode (designated as PBSPE) by flow injection analysis (FIA) in 0.1 M, pH 4 KCl/HCl carrier solution. The Prussian yellow/Prussian blue redox couple of the PBSPE was found to mediate the As(3+) oxidation. Various factors influencing the determination of As(3+) were thoroughly investigated in this study. Under the optimized FIA conditions, a linear calibration plot in the range of 50 nM-300 microM with a detection limit (S/N = 3) of 25 nM (i.e., 64.9 pg in 20-microL loop) was observed at an operation potential of +0.6 V vs Ag/AgCl. The sensitivity was good enough to detect arsenite at levels lower than the current EPA standard. This modified electrode showed good resistance to interference from common ions, especially Cl(-), which is generally considered as a major interference in the determination of As(3+) by ICPMS. The practical utility of the PBSPE to detect As(3+) was demonstrated in "blackfoot" disease endemic village groundwater from the southwestern coast area of Taiwan (Pei-Men).     

Microtubule sensors and sensor array based on polyaniline synthesized in the presence of poly(styrene sulfonate)

Microtubule sensors for glucose, urea, and triglyceride were fabricated based on poly(styrene sulfonate)-polyaniline (PSS-PANI) composites synthesized within the pores of track-etched polycarbonate membranes. The synthesis of a sufficiently thick and conducting PSS-PANI film at pH 5 provided the advantage of immobilizing enzymes during polymerization. This resulted in the improvement of sensor response for urea and triglyceride by a factor of approximately 10(2) with a significant increase in the linear region of response compared to polyaniline-based sensors, where the enzymes were immobilized by physical adsorption after the polymerization. The sensors based on urea and triglyceride were found to have a higher linear range of response, better sensitivity, improved multiple use capability, and faster response time compared to the potentiometric and amperometric sensors based on polyaniline. A microtubule sensor array for glucose, urea, and triglyceride based on PSS-PANI was fabricated by immobilization of three different sets of enzymes on three closely spaced devices and its response was found to be free from cross-interference when a sample containing a mixture of the above analytes was analyzed in a single measurement.