10 research outputs found

    Characteristics Of Laser-Induced Plasma As A Spectroscopic Light Emission Source

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    Laser-induced plasma is today a widespread spectroscopic emission source. It can be easily generated using compact and reliable nanosecond pulsed lasers and finds applications in various domains with laser-induced breakdown spectroscopy (LIBS). It is however such a particular medium which is intrinsically a transient and non-point light emitting source. Its timeand space-resolved diagnostics is therefore crucial for its optimized use. In this paper, we review our work on the investigation of the morphology and the evolution of the plasma. Different time scales relevant for the description of the plasma\u27s kinetics and dynamics are covered by suitable techniques. Our results show detailed evolution and transformation of the plasma with high temporal and spatial resolutions. The effects of the laser parameters as well as the background gas are particularly studied. © 2012 American Institute of Physics

    Qualidade pós-colheita da alface hidropônica em ambiente protegido sob malhas termorefletoras e negra

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    Considerando que a duração da exposição, a qualidade e intensidade de luz afetam as características de qualidade das hortaliças folhosas, conduziu-se um experimento, em ambiente protegido, com o objetivo de avaliar a qualidade pós-colheita da alface hidropônica, sob os efeitos das malhas de sombreamento, com diferentes percentagens de atenuação da radiação solar. O delineamento experimental foi o de blocos casualizados, no esquema fatorial 2 x 5, com três repetições, sendo os tratamentos constituídos por quatro malhas termorefletoras (40; 50; 60 e 70% de sombreamento) e uma testemunha, com malha negra 50%. Em cada parcela, representada por um sistema hidropônico individual, foi cultivada a alface (cv. Olinda, Crespa), sendo avaliada sua qualidade por ocasião da colheita e após quatro dias de armazenamento refrigerado (7,6 ± 1ºC e 27 ± 5 % UR). Observou-se que o excesso de sombreamento, ocasionado pelas malhas termorefletoras 60 e 70% e malha negra 50%, comprometeram a aparência da alface. As plantas submetidas ao sombreamento com a malha termorefletora 40% apresentaram menor perda de massa, ao final de quatro dias de armazenamento. Os graus de sombreamento ocasionados pelas malhas termorefletoras e pela malha negra não influenciaram nos teores de ácido cítrico, sólidos solúveis, vitamina C e clorofila total da alface

    Thrombin-receptor antagonist vorapaxar in acute coronary syndromes

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    BACKGROUND Vorapaxar is a new oral protease-activated–receptor 1 (PAR-1) antagonist that inhibits thrombin-induced platelet activation. METHODS In this multinational, double-blind, randomized trial, we compared vorapaxar with placebo in 12,944 patients who had acute coronary syndromes without ST-segment elevation. The primary end point was a composite of death from cardiovascular causes, myocardial infarction, stroke, recurrent ischemia with rehospitalization, or urgent coronary revascularization. RESULTS Follow-up in the trial was terminated early after a safety review. After a median follow-up of 502 days (interquartile range, 349 to 667), the primary end point occurred in 1031 of 6473 patients receiving vorapaxar versus 1102 of 6471 patients receiving placebo (Kaplan–Meier 2-year rate, 18.5% vs. 19.9%; hazard ratio, 0.92; 95% confidence interval [CI], 0.85 to 1.01; P = 0.07). A composite of death from cardiovascular causes, myocardial infarction, or stroke occurred in 822 patients in the vorapaxar group versus 910 in the placebo group (14.7% and 16.4%, respectively; hazard ratio, 0.89; 95% CI, 0.81 to 0.98; P = 0.02). Rates of moderate and severe bleeding were 7.2% in the vorapaxar group and 5.2% in the placebo group (hazard ratio, 1.35; 95% CI, 1.16 to 1.58; P<0.001). Intracranial hemorrhage rates were 1.1% and 0.2%, respectively (hazard ratio, 3.39; 95% CI, 1.78 to 6.45; P<0.001). Rates of nonhemorrhagic adverse events were similar in the two groups. CONCLUSIONS In patients with acute coronary syndromes, the addition of vorapaxar to standard therapy did not significantly reduce the primary composite end point but significantly increased the risk of major bleeding, including intracranial hemorrhage
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