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The effects of UV-assisted TiO2-photocatalytic oxidation (PCO) inactivation of pathogenic bacteria (Escherichia coli O157:H7, Listeria monocytogenes, Salmonella typhimurium) in a liquid culture using different domains of UV irradiation (A, B and C) were evaluated. Structural changes in super-coiled plasmid DNA (pUC19) and genomic DNA of E. coli were observed using gel electrophoresis to demonstrate the photodynamic DNA strand breaking activity of UV-assisted TiO2-PCO. Membrane damage in bacterial cells was observed using both a scanning electron microscope (SEM) and a confocal laser scanning microscope (CLSM). Both UVC-TiO2-PCO and UVC alone resulted in an earlier bactericidal phase (initial counts of approximately 6 log CFU/mL) in 60 s and 90 s, respectively, in liquid culture. UVC-TiO2-PCO treatment for 6 min converted all plasmid DNA to the linear form; however, under UVC irradiation alone, super-coiled DNA remained. Prolonged UVC-TiO2-PCO treatment resulted in structural changes in genomic DNA from E. coli. SEM observations revealed that bacteria suffered severe visible cell damage after UVC-TiO2-PCO treatment for 30–60 min. S. typhimurium cells showed visible damage after 30 min, which was confirmed using CLSM. All treated cells were stained red using propidium iodide under a fluorescent light.  相似文献   
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Telecommunication Systems - Integration of optical and millimeter-wave systems provide a promising solution for future giga-bits per second wireless communication systems. We have proposed and...  相似文献   
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An efficient and robust numerical scheme based on Haar wavelets and finite differences is suggested for the solution of two-dimensional time dependent linear and nonlinear partial differential equations (PDEs). Excellent feature of the scheme is the conversion of linear and non-linear PDEs to algebraic equations which are comparatively easy to handle. Convergence of the scheme, which guarantees small error norm as the resolution level increases, is also an important part of this work. Different error norms are computed to check efficiency of the technique. Computations verify accuracy, flexibility and low computational cost of the method.  相似文献   
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One of the most important manufacturing steps of the rod end materials is the induction process by which the both hardness of the surfaces and the toughness of the part can be adjusted at the same time. In the study, rod end materials which are inducted and non-inducted are simulated in the view of the fatigue life properties. In the simulations, the rod end parts are defined as functionally graded materials where the mechanical properties of the materials are varying with the dimensions. Additionally, the noninducted material properties or fully strengthened material properties are defined for the geometry in order to comprehend the contribution of the definitions on the congruity of the finite element simulation results with the experiments. When the materials properties of the rod end part are defined as functional graded, the simulation results are found to be much more close to the experimental results.

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Recently, a newly discovered Dicer-substrate siRNA (DsiRNA) demonstrates higher potency in gene silencing than siRNA but both suffer from rapid degradation, poor cellular uptake and chemical instability. Therefore, Tat-peptide was exploited to protect and facilitate their delivery into cells. In this study, Tat-peptide was complexed with siRNA or DsiRNA through simple complexation. The physicochemical properties (particle size, surface charge and morphology) of the complexes formed were then characterized. The ability of Tat-peptide to carry and protect siRNA or DsiRNA was determined by UV-Vis spectrophotometry and serum protection assay, respectively. Cytotoxicity effect of these complexes was assessed in V79 cell line. siRNA-Tat complexes had particle size ranged from 186?±?17.8 to 375?±?8.3?nm with surface charge ranged from ?9.3?±?1.0 to +13.5?±?1.0?mV, depending on the Tat-to-siRNA concentration ratio. As for DsiRNA-Tat complexes, the particle size was smaller than the ones complexed with siRNA, ranging from 176?±?8.6 to 458?±?14.7?nm. Their surface charge was in the range of +27.1?±?3.6 to +38.1?±?0.9?mV. Both oligonucleotide (ON) species bound strongly to Tat-peptide, forming stable complexes with loading efficiency of more than 86%. These complexes were relatively non cytotoxic as the cell viability of ~90% was achieved. In conclusion, Tat-peptide has a great potential as siRNA and DsiRNA vector due to the formation of stable complexes with desirable physical characteristics, low toxicity and able to carry high amount of siRNA or DsiRNA.  相似文献   
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