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Träfflista för sökning "WFRF:(Rasmuson Johan) srt2:(2015-2019)"

Sökning: WFRF:(Rasmuson Johan) > (2015-2019)

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2.
  • Li, Liang, 1987, et al. (författare)
  • Effect of drag models on residence time distributions of particles in a wurster fluidized bed: A DEM-CFD study
  • 2016
  • Ingår i: KONA Powder and Particle Journal. - : Hosokawa Powder Technology Foundation. - 0288-4534 .- 2187-5537. ; 2016:33, s. 264-277
  • Tidskriftsartikel (refereegranskat)abstract
    • Fluidized bed coating has been used to coat pellets or tablets with functional substances for a number of purposes. In this coating process, particle wetting, drying and film formation are coupled to particle motion. It is therefore of interest to study particle motion in such fluidized beds and to use the results to develop a model for predicting the quality of the final product. In this paper, we present results from DEM-CFD simulations, i.e. discrete element method and computational fluid dynamics simulations of particle motion in a laboratory-scale Wurster fluidized bed that was also employed in positron emission particle tracking (PEPT) experiments. As the drag force is the dominant interaction between the gas flow and the particle motion in this type of fluidized bed, the effect of drag models on the particle motion is investigated. More specifically, the particle velocity and residence time distributions of particles in different regions calculated from five different drag models are presented. It is found that the Gidaspow and Tang drag models predict both particle cycle and residence times well. The HKL and Beetstra drag models somewhat overestimate the particle velocity in the Wurster tube and therefore predict a reduced number of recirculations and a significantly shorter cycle time.
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3.
  • Li, Liang, 1987, et al. (författare)
  • PEPT Study of Particle Cycle and Residence Time Distributions in a Wurster Fluid Bed
  • 2015
  • Ingår i: AICHE Journal. - : Wiley. - 1547-5905 .- 0001-1541. ; 61:3, s. 756-768
  • Tidskriftsartikel (refereegranskat)abstract
    • Particle cycle and residence time distributions are critical factors in determining the coating quality in the Wurster process. Positron emission particle tracking experiments are performed to determine the cycle and residence times of particles in different regions of a Wurster fluid bed. The results show that particles tend to recirculate in and sneak out below from the Wurster tube. The experiments also show that a larger batch size leads to a shorter cycle time and a narrower cycle time distribution (CTD). It is possible to avoid recirculations and obtain a shorter cycle time and a narrower CTD by selecting the operating conditions appropriately or via equipment design. Experiments using binary mixtures of particles with a diameter ratio of 1.5 show that large particles have a longer cycle time than small particles and that the cycle time is shorter for mixtures with approximately equal amounts of small and large particles.
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4.
  • Li, Liang, 1987, et al. (författare)
  • Residence time distributions of different size particles in the spray zone of a Wurster fluid bed studied using DEM-CFD
  • 2015
  • Ingår i: Powder Technology. - : Elsevier BV. - 1873-328X .- 0032-5910. ; 280, s. 124-134
  • Tidskriftsartikel (refereegranskat)abstract
    • Particle cycle and residence time distributions in different regions, particularly in the spray zone, play an important role in fluid bed coating. In this study, a DEM-CFD (discrete element method, computational fluid dynamics) model is employed to determine particle cycle and residence time distributions in a laboratory-scale Wurster fluid bed coater. The calculations show good agreement with data obtained using the positron emission particle tracking (PEPT) technique. The DEM-CFD simulations of different size particles show that large particles spend a longer time in the spray zone and in the Wurster tube than small particles. In addition, large particles are found on average to move closer to the spray nozzle than small particles, which implies that the large particles could shield small particles from the spray droplets. Both of these effects suggest that large particles receive a greater amount of coating solution per unit area per cycle than small particles. However, the simulations in combination with the PEPT experiments show that this is partly compensated for by a longer cycle time for large particles. Large particles thus receive more coating per unit area per pass through the spray zone, but also travel through the spray zone less frequently than small particles.
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6.
  • Rasmuson, Johan (författare)
  • Cardiopulmonary involvement in Puumala hantavirus infection
  • 2015
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Puumala hantavirus (PUUV) causes hemorrhagic fever with renal syndrome in Europe. After inhalation of virus shed by bank voles, the virus systemically targets the vascular endothelium leading to vascular dysfunction and leakage. Many patients with PUUV infection experience cardiopulmonary manifestations but the underlying mechanisms have not been determined.The aims of the studies presented were to describe cardiopulmonary manifestations, investigate pathogenetic mechanisms including presence of virus in the lungs and the local immune response in PUUV infection.The results showed cardiopulmonary involvement of varying severity in almost all studied patients. High-resolution computed tomography frequently revealed vascular leakage into the lungs or pleural cavities. Pulmonary function tests generally showed reduced gas diffusing capacity, evidenced in patients as dyspnea, poor oxygenation and frequent need of oxygen treatment. Among patients who were not fully recovered at 3 months follow-up, remaining decreased gas diffusing capacity was highly common.Echocardiography revealed mainly right heart dysfunction which was related to manifestations within the lungs, in terms of increased estimated pulmonary vascular resistance, mild to moderate pulmonary hypertension, and reduced right ventricular systolic function in patients with more pronounced lung involvement, as indicated by need of oxygen treatment.Analyses on bronchoalveolar lavage (BAL) and bronchial biopsies revealed a highly activated cytotoxic T cell (CTL) response in the lungs. The CTL response was not balanced by the expansion of regulatory T cells and high numbers of CTLs were associated with more severe disease. PUUV RNA was detected in almost all patients’ BAL samples and the viral load was inversely correlated to the number of CTLs.Three patients presenting with severe and fatal cardiopulmonary distress were also described. Autopsies revealed PUUV protein in vascular endothelium in all investigated organs, including the heart and lungs, along with a massive CTL response mainly in the lungs.In conclusion, cardiopulmonary involvement of varying severity was present in almost all patients with PUUV infection. Cytotoxic immune responses could contribute to disease development but also help in clearing the infection. Long lasting fatigue after hantavirus infection may be explained by remaining manifestations within the lungs. 
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7.
  • Rasmuson, Johan, 1977-, et al. (författare)
  • Cytotoxic immune responses in the lungs correlate to disease severity in patients with hantavirus infection
  • 2016
  • Ingår i: European Journal of Clinical Microbiology and Infectious Diseases. - : Springer Science and Business Media LLC. - 0934-9723 .- 1435-4373. ; 35:4, s. 713-721
  • Tidskriftsartikel (refereegranskat)abstract
    • Hantavirus infections may cause severe and sometime life-threatening lung failure. The pathogenesis is not fully known and there is an urgent need for effective treatment. We aimed to investigate the association between pulmonary viral load and immune responses, and their relation to disease severity. Bronchoscopy with sampling of bronchoalveolar lavage (BAL) fluid was performed in 17 patients with acute Puumala hantavirus infection and 16 healthy volunteers acting as controls. Lymphocyte subsets, granzyme concentrations, and viral load were determined by flow cytometry, enzyme-linked immunosorbent assay (ELISA), and quantitative reverse transcription polymerase chain reaction (RT-PCR), respectively. Analyses of BAL fluid revealed significantly higher numbers of activated CD8+ T cells and natural killer (NK) cells, as well as higher concentrations of the cytotoxins granzymes A and B in hantavirus-infected patients, compared to controls. In patients, Puumala hantavirus RNA was detected in 88 % of BAL cell samples and correlated inversely to the T cell response. The magnitude of the pulmonary cytotoxic lymphocyte response correlated to the severity of disease and systemic organ dysfunction, in terms of need for supplemental oxygen treatment, hypotension, and laboratory data indicating renal failure, cardiac dysfunction, vascular leakage, and cell damage. Regulatory T cell numbers were significantly lower in patients compared to controls, and may reflect inadequate immune regulation during hantavirus infection. Hantavirus infection elicits a pronounced cytotoxic lymphocyte response in the lungs. The magnitude of the immune response was associated with disease severity. These results give insights into the pathogenesis and possibilities for new treatments.
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8.
  • Scholz, Saskia, et al. (författare)
  • Human hantavirus infection elicits pronounced redistribution of mononuclear phagocytes in peripheral blood and airways
  • 2017
  • Ingår i: PLoS Pathogens. - : Public library science. - 1553-7366 .- 1553-7374. ; 13:6
  • Tidskriftsartikel (refereegranskat)abstract
    • Hantaviruses infect humans via inhalation of virus-contaminated rodent excreta. Infection can cause severe disease with up to 40% mortality depending on the viral strain. The virus primarily targets the vascular endothelium without direct cytopathic effects. Instead, exaggerated immune responses may inadvertently contribute to disease development. Mononuclear phagocytes (MNPs), including monocytes and dendritic cells (DCs), orchestrate the adaptive immune responses. Since hantaviruses are transmitted via inhalation, studying immunological events in the airways is of importance to understand the processes leading to immunopathogenesis. Here, we studied 17 patients infected with Puumala virus that causes a mild form of hemorrhagic fever with renal syndrome (HFRS). Bronchial biopsies as well as longitudinal blood draws were obtained from the patients. During the acute stage of disease, a significant influx of MNPs expressing HLA-DR, CD11c or CD123 was detected in the patients' bronchial tissue. In parallel, absolute numbers of MNPs were dramatically reduced in peripheral blood, coinciding with viremia. Expression of CCR7 on the remaining MNPs in blood suggested migration to peripheral and/or lymphoid tissues. Numbers of MNPs in blood subsequently normalized during the convalescent phase of the disease when viral RNA was no longer detectable in plasma. Finally, we exposed blood MNPs in vitro to Puumala virus, and demonstrated an induction of CCR7 expression on MNPs. In conclusion, the present study shows a marked redistribution of blood MNPs to the airways during acute hantavirus disease, a process that may underlie the local immune activation and contribute to immunopathogenesis in hantavirus-infected patients.
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9.
  • Sironen, Tarja, et al. (författare)
  • Fatal Puumala Hantavirus Disease : Involvement of Complement Activation and Vascular Leakage in the Pathobiology
  • 2017
  • Ingår i: Open Forum Infectious Diseases. - : Oxford University Press. - 2328-8957. ; 4:4
  • Tidskriftsartikel (refereegranskat)abstract
    • The case-fatality rate of hantavirus disease depends strongly on the causative hantavirus, ranging from 0.1% to 40%. However, the pathogenesis is not fully understood, and at present no licensed therapies exist. We describe fatal cases caused by Puumala hantavirus indicating involvement of complement activation and vascular leakage.
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