275 research outputs found

    Nanoparticle synthesis using high-powered pulse-modulated induction thermal plasma

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    金沢大学理工研究域電子情報学系Nanoparticle synthesis was performed using the high-powered pulse-modulated induction thermal plasma (PMITP) technique to study the effect of coil current modulation on synthesized nanoparticles. This is the first paper to present a summary of results of TiO2 nanoparticle synthesis using high-power Ar-O2 PMITP at 20 kW. The synthesized particles were analysed using field emission scanning electron microscopy and X-ray diffractometry. In addition, optical emission spectroscopy was used during nanoparticle synthesis experiments to measure TiO spectra and to determine the time-averaged vibrational and rotational temperatures of TiO in the reaction chamber. The results showed that the PMITP produced smaller nanoparticles and a narrower size distribution of particles. Moreover, PMITP provided a lower temperature region in the reaction chamber downstream of the plasma torch than such regions in non-modulated thermal plasmas. © 2010 IOP Publishing Ltd

    Clinical Evaluation of the Peroral Cholangioscopy Using a New Videoscope

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    Peroral cholangioscopy (PCS) has been performed in 22 cases using XCHF-B200 (Olympus Optical Co.) since June 1995 and in 77 cases using CHF-B20 (Olympus Optical Co.) after EST from Jan. 1989. XCHF-B200 has a longer rigid portion of distal end and a smaller channel diameter than CHF-B20. The successful rate of PCS using XCHF-B200 (82%) was lower than that of CHF-B20 (89%). The vascular pattern and fine vertical groove of the bile duct mucosa were shown more clearly on the photographs obtained with XCHF-B200 than those obtained with CHF-B20. However, not enough biopsy specimens could be obtained because the channel diameter of XCHF-B200 was rather small

    Molecular characterization and validation of commercially available methods for haptoglobin measurement in bottlenose dolphin

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    AbstractHaptoglobin (Hp) is a positive acute-phase protein and a valuable marker of inflammation in both human and veterinary medicine. The aim of this study was to validate the molecular characterization of Hp in dolphins and to validate commercially available Hp measurement methods such as Hp-ELISA (originally designed for pigs) and Hp–hemoglobin (Hb) binding assay. The dolphin Hp (dHp) amino acid sequence appeared most similar to pig Hp by sequence homology and phylogenetic clustering. Amino acid sequence analysis revealed that dHp comprises the Hp1 form of α1 and β chains. The anti-pig Hp antibody cross-reacted with both recombinant dHp, expressed by Escherichia coli, and dHp from serum. The intra- and inter-assay levels of imprecision of pig Hp-ELISA and the Hp–Hb binding assay were found to be tolerable for the determination of Hp in dolphin, and there was no significant discrepancy between the two determination methods. The ability of the assay to differentiate between healthy and inflammation groups was investigated, and a significant increase in Hp concentration was detected in inflammatory conditions. Thus, Hp is a useful inflammation marker for dolphin, and the Hp concentration in dolphin serum samples can be reliably measured using commercially available pig Hp-ELISA and Hp–Hb binding assay

    Molecular epidemiology of livestock rabies viruses isolated in the northeastern Brazilian states of Paraíba and Pernambuco from 2003 - 2009

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    <p>Abstract</p> <p>Background</p> <p>Limited or no epidemiological information has been reported for rabies viruses (RABVs) isolated from livestock in the northeastern Brazilian states of Paraíba (PB) and Pernambuco (PE). The aim of this study was to clarify the molecular epidemiology of RABVs circulating in livestock, especially cattle, in these areas between 2003 and 2009.</p> <p>Findings</p> <p>Phylogenetic analysis based on 890 nt of the nucleoprotein (N) gene revealed that the 52 livestock-derived RABV isolates characterized here belonged to a single lineage. These isolates clustered with a vampire bat-related RABV lineage previously identified in other states in Brazil; within PB and PE, this lineage was divided between the previously characterized main lineage and a novel sub-lineage.</p> <p>Conclusions</p> <p>The occurrences of livestock rabies in PB and PE originated from vampire bat RABVs, and the causative RABV lineage has been circulating in this area of northeastern Brazil for at least 7 years. This distribution pattern may correlate to that of a vampire bat population isolated by geographic barriers.</p

    Molecular epidemiological tracing of a cattle rabies outbreak lasting less than a month in Rio Grande do Sul in southern Brazil

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    Abstract\ud \ud Background\ud Vampire bat-transmitted cattle rabies cases are typically encountered in areas where the disease is endemic. However, over the period of a month in 2009, an outbreak of cattle rabies occurred and then ended spontaneously in a small area of the Rio Grande do Sul State in southern Brazil. To investigate the epidemiological characteristics of this rabies outbreak in Rio Grande do Sul, 26 nucleotide sequences of rabies virus (RABV) genomes that were collected in this area were analyzed phylogenetically.\ud \ud \ud Results\ud Nucleotide sequence identities of the nucleoprotein gene and G–L intergenic region of the 26 RABVs were greater than 99.6 %. Phylogenetic analysis showed that all RABVs clustered with the vampire bat-related cattle RABV strains and that the RABVs were mainly distributed in southern Brazil.\ud \ud \ud Conclusions\ud The findings of the present study suggested that a small population of rabid vampire bats carrying a single RABV strain produced a spatiotemporally restricted outbreak of cattle rabies in southern Brazil.This study was supported in part by a Grant-in-Aid for Scientific Research\ud (24580453) from the Japan Society for the Promotion of Science and the\ud Strategic Research Base Development Program, “International joint research\ud and training of young researchers for zoonosis control in a globalized world”,\ud and a matching fund subsidy from the Ministry of Education, Culture, Sports,\ud Science and Technology of Japan (S0991023 and S1491007)
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