Global ETD Search

21	Measurements of 2π<sup>0</sup> and 3π<sup>0</sup> Production in Proton-Proton Collisions at a Center of Mass Energy of 2.465 GeV Koch, Inken January 2004 (has links) <p>Neutral two- and three-pion productions in proton-proton collisions at a center of mass energy of 2.465 GeV have been studied using the WASA detector and an internal pellet target at the CELSIUS storage ring in Uppsala. An important part of the detector for the measurments was a central electromagnetic calorimeter composed of 1012 CsI crystals, which measured the photons originating from neutral pion decays. Test measurements and calibration procedures for this detector part were carried out. An important part of the analysis was the identification of the neutral pions from the invariant mass of the decay gammas and the use of Monte Carlo simulations to understand the detector responds.</p><p>Total cross sections for the pp→ppπ<sup>0</sup>π<sup>0</sup> and pp→ppπ<sup>0</sup>π<sup>0</sup>π<sup>0</sup> reactions are presented as well as distributions of relevant kinematical variables for the pp→ppπ<sup>0</sup>π<sup>0</sup> reaction.</p><p>The distributions show significant deviations from phase space predictions. These deviations are typical for resonance production. The excitation of two simultaneous Δ resonances seems to be the main reaction mechanism. </p> Radiation sciences two pion three pion production WASA Celsius cross section calorimeter CsI crystals kinematical distribution Strålningsvetenskap Radiation biology Strålningsbiologi
22	Measurements of 2π0 and 3π0 Production in Proton-Proton Collisions at a Center of Mass Energy of 2.465 GeV Koch, Inken January 2004 (has links) Neutral two- and three-pion productions in proton-proton collisions at a center of mass energy of 2.465 GeV have been studied using the WASA detector and an internal pellet target at the CELSIUS storage ring in Uppsala. An important part of the detector for the measurments was a central electromagnetic calorimeter composed of 1012 CsI crystals, which measured the photons originating from neutral pion decays. Test measurements and calibration procedures for this detector part were carried out. An important part of the analysis was the identification of the neutral pions from the invariant mass of the decay gammas and the use of Monte Carlo simulations to understand the detector responds. Total cross sections for the pp→ppπ0π0 and pp→ppπ0π0π0 reactions are presented as well as distributions of relevant kinematical variables for the pp→ppπ0π0 reaction. The distributions show significant deviations from phase space predictions. These deviations are typical for resonance production. The excitation of two simultaneous Δ resonances seems to be the main reaction mechanism. Radiation sciences two pion three pion production WASA Celsius cross section calorimeter CsI crystals kinematical distribution Strålningsvetenskap Radiation biology Strålningsbiologi
23	Accurate description of heterogeneous tumors for biologically optimized radiation therapy Nilsson, Johan January 2004 (has links) In this thesis, a model of tissue oxygenation is presented, that takes into account the heterogeneous nature of tumor vasculature. Even though the model is rather simple, the resulting oxygen distributions agree very well with clinically observed oxygen distributions for most tumors and healthy normal tissues. The model shows that the vascular density may not describe the oxygenation of a tissue sufficiently well, unless the heterogeneity of the vascular system is taken into account. Based on the oxygen distributions from the tissue model, the associated radiation response at low and high doses can be determined. The radiation response of heterogeneous tumors should preferably be described by two clonogen compartments, one resistant and one sensitive, dominating the response at high and low radiation doses, respectively. Furthermore, each compartment should be characterized by the effective radiation resistance and the effective clonogen number. The resistant-sensitive model of radiation response has been analyzed in great detail. It accurately describes the response of severely heterogeneous tumors, both at low and high doses and LET values. The effective response parameters are given as integrals, averaged over the whole spectrum of radiation resistance. The parameters can also be determined from clinically established dose-response relations. The main properties of the dose-response relation for a generally heterogeneous tumor is described in some detail. The normalized dose-response gradient has been generalized to take heterogeneities in both dose delivery and radiation response into account. This quantity is important for accurate treatment plan optimization using intensity modulated radiation therapy for individual patients. heterogeneous tumors radiation therapy biological optimization tumor hypoxia effective radiation sensitivity effective radiation resistance Radiation biology Strålningsbiologi
24	Energy and intensity modulated radiation therapy with electrons Olofsson, Lennart January 2005 (has links) In recent years intensity modulated radiation therapy with photons (xIMRT) has gained attention due to its ability to reduce the dose in the tissues close to the tumour volume. However, this technique also results in a large low dose volume. Electron IMRT (eIMRT) has the potential to reduce the integral dose to the patient due to the dose fall off in the electron depth dose curves. This dose fall off makes it possible to modulate the dose distribution in the direction of the beam by selecting appropriate electron energies. The use of a computer based energy selection method was examined in combination with the IMRT technique to optimise the electron dose distribution. It is clearly illustrated that the energy optimisation procedure reduces the dose to lung and heart in a breast cancer treatment. To shape the multiple electron subfields (beamlets) that are used in eIMRT, an electron multi leaf collimator (eMLC) is needed. However, photons produced in a conventional electron treatment head could penetrate such an added eMLC, thus producing an undesirable dose contribution. The leakage levels normally achieved are acceptable for standard single electron field treatments but could become unacceptably high in eIMRT treatments where a lot of small subfields are combined. To limit this photon contribution, the photon MLC (xMLC) was used to shield off large parts of the photon leakage. The effect of this xMLC shielding on the reduction of photon leakage, the electron beam penumbras, and electron output (dose level), was studied using Monte Carlo methods for different electron treatment head designs. The use of helium as a mean to reduce the electron scatter in the treatment head, and thus the perturbating effect of the xMLC on electron beam penumbra and output, was also investigated. This thesis shows that the effect of the xMLC shielding on the electron beam penumbra and output can be made negligible while still obtaining a significantly reduced x-ray leakage dose contribution. The result is a large gain in radiation protection of the patient and a better dynamic range for the eIMRT dose optimisation. For this optimisation a computer based electron energy selection method was developed and tested on two clinical cases. Radiation sciences Radiation therapy Conformal therapy IMRT Electrons Electron treatment head Electron MLC Bremsstrahlung reduction Integral dose Penumbra Output factor Strålningsvetenskap Radiation biology Strålningsbiologi
25	Molecular Radionuclide Imaging Using Site-specifically Labelled Recombinant Affibody Molecules : Preparation and Preclinical Evaluation Ahlgren, Sara January 2010 (has links) Radionuclide molecular imaging is an emerging multidisciplinary technique that is used in modern medicine to visualise diseases at cellular and molecular levels. This thesis is based on five papers (I-V) and focuses on the development of site-specific radiolabelled recombinant anti-HER2 Affibody molecules and preclinical evaluations in vitro and in vivo of the labelled conjugates. This work is part of a preclinical development of an Affibody molecule-based tracer for molecular imaging of HER2 expressing tumours. Papers I and II report the evaluation of the Affibody molecule ZHER2:2395-C, site-specifically labelled with the radiometals 111In (for SPECT) and 57Co (as a surrogate for 55Co, suitable for PET applications) using a thiol reactive DOTA derivative as a chelator. Both conjugates demonstrated very suitable biodistribution properties, enabling high contrast imaging just a few hours after injection. Papers III and IV report the development and optimization of a technique for site-specific labelling of ZHER2:2395-C with 99mTc using an N3S chelating peptide sequence. 99mTc-ZHER2:2395-C demonstrated high and specific tumour uptake and rapid clearance of non-bound tracer from the blood, resulting in high tumour-to-non-tumour ratios shortly after injection, enabling high contrast imaging. In addition, in the study described in paper IV, freeze-dried kits previously developed for 99mTc-labelling were optimised, resulting in the development of a kit in which all the reagents and protein needed for labelling of ZHER2:2395-C with 99mTc were contained in a single vial. Paper V reports the evaluation of an anti-HER2 Affibody molecule, ABY-025, with a fundamentally re-engineered scaffold. Despite the profound re-engineering, the biodistribution pattern of 111In-ABY-025 was very similar to that of two variants of the parental molecule. It seems reasonable to believe that these results will also be applicable to Affibody molecules towards other targets. Hopefully, this work will also be helpful in the development of other small proteinaceous tracers. molecular radionuclide imaging Affibody molecules HER2 cancer detection radiolabelling technetium indium cobalt SPECT PET Oncology Onkologi Diagnostic radiology Diagnostisk radiologi Radiation biology Strålningsbiologi
26	Positron Emission Tomography (PET) Studies in Anxiety Disorders Michelgård Palmquist, Åsa January 2010 (has links) Anxiety disorders are very common and the primary feature is abnormal or inappropriate anxiety. Fear and anxiety is often mediated by the amygdala, a brain structure rich in substance P (SP) and neurokinin 1 (NK1) receptors. To learn more about how the human amygdala is modulated by fear and anxiety in event-triggered anxiety disorders and to investigate if the SP/NK1 receptor system is affected, regional cerebral blood flow (rCBF) ([15O]-water; Study I and II) and the SP/NK1 receptor system ([11C]GR205171; Study III and IV) were studied with positron emission tomography (PET). In Study I we investigated the neural correlates of affective startle modulation in persons with specific phobia by measuring rCBF during exposure to fearful and non-fearful pictures, paired and unpaired with acoustic startle stimuli. Fear-potentiated startle was associated with activation of the affective part of the anterior cingulate cortex and the left amygdaloid–hippocampal area. In Study II short-term drug treatment effects on rCBF in patients diagnosed with social phobia was evaluated, comparing the NK1 receptor antagonist GR205171 to the selective serotonin reuptake inhibitor citalopram and placebo. Social anxiety and neural activity in the medial temporal lobe including the amygdala was significantly reduced by both drugs but not placebo. In Study III we investigated if activity in the SP/NK1 receptor system in the amygdala would be affected by fear provocation in individuals with specific snake or spider phobia. Fear provocation was associated with a decreased uptake of the NK1 antagonist [11C]GR205171 in the amygdala, possibly explained by an increase in endogenous SP release occupying the NK1 receptors. Study IV was conducted to explore the resting state NK1 receptor availability in PTSD patients as compared to healthy controls. Increased resting state binding of the tracer [11C]GR205171 in the amygdala of patients with PTSD suggested an increased amount of available receptors. In summary, fear and fear-potentiated startle modulates the human amygdala, possibly through the SP/NK1 receptor system. Positron emission tomography PET amygdala fear anxiety anxiety disorders specific phobia social phobia posttraumatic stress disorder PTSD regional cerebral blood flow rCBF substance P SP neurokinin 1 receptor NK1 GR205171 STAI-S Psychiatry Psykiatri Neurobiology Neurobiologi Neuroscience Neurovetenskap Experimental brain research Experimentell hjärnforskning Molecular neurobiology Molekylär neurobiologi Radiation biology Strålningsbiologi Neurobiology Neurobiologi Neurobiology Neurobiologi

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