The targeted delivery of multicomponent cargos to cancer cells by nanoporous particle-supported lipid bilayers

Encapsulation of drugs within nanocarriers that selectively target malignant cells promises to mitigate side effects of conventional chemotherapy and to enable delivery of the unique drug combinations needed for personalized medicine. To realize this potential, however, targeted nanocarriers must simultaneously overcome multiple challenges, including specificity, stability and a high capacity for disparate cargos. Here we report porous nanoparticle-supported lipid bilayers (protocells) that synergistically combine properties of liposomes and nanoporous particles. Protocells modified with a targeting peptide that binds to human hepatocellular carcinoma exhibit a 10,000-fold greater affinity for human hepatocellular carcinoma than for hepatocytes, endothelial cells or immune cells. Furthermore, protocells can be loaded with combinations of therapeutic (drugs, small interfering RNA and toxins) and diagnostic (quantum dots) agents and modified to promote endosomal escape and nuclear accumulation of selected cargos. The enormous capacity of the high-surface-area nanoporous core combined with the enhanced targeting efficacy enabled by the fluid supported lipid bilayer enable a single protocell loaded with a drug cocktail to kill a drug-resistant human hepatocellular carcinoma cell, representing a 10(6)-fold improvement over comparable liposomes.     

Quantitative investigation of soot distribution by laser-induced incandescence

Strategies employed for quantitative measurement by laser-induced incandescence are detailed. Data are obtained for several laminar diffusion flames formed from blended Diesel fuels of known composition. A tomographic procedure is developed to scale the two-dimensional data to soot volume fraction and to correct for the trapping of signal by the soot field. Scaling is achieved by use of laser extinction along the measurement plane. The findings are used in discussions of measurement issues within turbulent environments. Data are augmented with elastic scattering measurements, allowing particle-size and number-density distributions to be inferred. A degree of axial and radial similarity among various flames suggests that the processes of soot formation and oxidation occur over similar time scales for each fuel.     

Pervaporation as an alternative to headspace

The use of pervaporation as an alternative to headspace is proposed. The analytical system involves the speciation of organomercury compounds in solid samples using pervaporation, which has been coupled for the first time to gas chromatography. The speciation of mercury as Me(2)Hg, Et(2)Hg, and MeHgCl has been carried out without any derivatization of the analytes, which, after separation from the solid matrix, are preconcentrated on a Tenax minicolumn prior to desorption and chromatographic separation on a semicapillary column (HP-1) prior to atomic fluorescence detection. No column degradation was observed. Linear ranges and detection limits slightly better than those obtained by headspace GC were observed for mercury species in solid samples. Excellent recoveries (between 95 and 107%) for mercury species added to complex solid samples were obtained by this extremely simple and easily automated setup.     

Inhibitory Effect of Fusarium Mycotoxins on Growth of Brewing Yeasts. 2. Deoxynivalenol and Nivalenol*

The effect of the trichothecene mycotoxins deoxynivalenol (DON) and nivalenol (NIV) on growth of Saccharomyces cerevisiae lager and ale strains has been studied. The toxins were added into the growth medium in low and high concentrations. Yeast growth was assessed by measurement of dry weight or relative growth, cell number, viability and conductance change of the growth medium using direct and indirect methods. The inhibitory effect of both DON and NIV on yeast growth was dependent on toxin concentration. Additionally, when the extent of inhibition of yeast growth caused by high concentrations of both toxins was observed, it was subject to yeast strain, length of incubation and method used to assess yeast growth. The lowest concentrations of mycotoxin causing significant inhibition on growth of brewing yeasts were: 100 μg/ml DON for the lager strain and 50 μg/ml for the ale strain, and 50 μg/ml NIV for the ale strain.