180 research outputs found
Feasibility Studies for the Panda Experiment at Fair
PANDA, the detector to study AntiProton ANnihilations at DArmstadt, will be
installed at the future international Facility for Anti-proton and Ion Research
(FAIR) in Darmstadt, Germany. The PANDA physics program is oriented towards the
studies of the strong interaction and hadron structure performed with the
highest quality beam of anti-protons [1]. In the preparation for PANDA
experiments, large-scale simulation studies are being performed to validate the
performance of all individual detector components and to advice on detector
optimisation. The feasibility of the analysis strategies together with the
calibration methods are being studied. Simulations were carried out using the
framework called PandaROOT [2], based on ROOT and the Virtual Monte Carlo
concept [3].
[1] http://www-panda.gsi.de; Technical Progress Report (2005); Physics
Performance Report (2009), arXiv:0903.3905v1.
[2] [PANDA Collaboration] S. Spataro, J. Phys. 119, 032035 (2008).
[3] http://root.cern.chComment: Proceeding of the XXXI Mazurian Lakes Conference on Physics, Piaski,
30.08-6.09, 200
Proton radiography to improve proton radiotherapy: Simulation study at different proton beam energies
To improve the quality of cancer treatment with protons, a translation of
X-ray Computed Tomography (CT) images into a map of the proton stopping powers
needs to be more accurate. Proton stopping powers determined from CT images
have systematic uncertainties in the calculated proton range in a patient of
typically 3-4\% and even up to 10\% in region containing
bone~\cite{USchneider1995,USchneider1996,WSchneider2000,GCirrone2007,HPaganetti2012,TPlautz2014,GLandry2013,JSchuemann2014}.
As a consequence, part of a tumor may receive no dose, or a very high dose can
be delivered in healthy ti\-ssues and organs at risks~(e.g. brain
stem)~\cite{ACKnopf2013}. A transmission radiograph of high-energy protons
measuring proton stopping powers directly will allow to reduce these
uncertainties, and thus improve the quality of treatment.
The best way to obtain a sufficiently accurate radiograph is by tracking
individual protons traversing the phantom
(patient)~\cite{GCirrone2007,TPlautz2014,VSipala2013}. In our simulations we
have used an ideal position sensitive detectors measuring a single proton
before and after a phantom, while the residual energy of a proton was detected
by a BaF crystal. To obtain transmission radiographs, diffe\-rent phantom
materials have been irradiated with a 3x3~cm scattered proton beam, with
various beam energies. The simulations were done using the Geant4 simulation
package~\cite{SAgostinelli2003}.
In this study we focus on the simulations of the energy loss radiographs for
various proton beam energies that are clinically available in proton
radiotherapy.Comment: 6 pages, 6 figures, Presented at Jagiellonian Symposium on
Fundamental and Applied Subatomic Physics, 7-12 June, 2015, Krak\'ow, Polan
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Printability study of metal ion crosslinked PEG-catechol based inks
In this paper we explore the printability of reversible networks formed by catechol functionalized PEG solutions and metal cations (Al3+, Fe3+ or V3+). The printability and shape fidelity were dependent on the ink composition (metal ion type, pH, PEG molecular weight) and printing parameters (extrusion pressure and printing speed). The relaxation time, recovery rate and viscosity of the inks were analyzed in rheology studies and correlated with thermodynamic and ligand exchange kinetic constants of the dynamic bonds and the printing performance (i.e. shape fidelity of the printed structures). The relevance of the relaxation time and ligand exchange kinetics for printability was demonstrated. Cells seeded on the materials crosslinked with Al3+, Fe3+ ions were viable and revealed well-spread morphologies during 7 day culture, indicating the potential of the formulations to be used as inks for cell encapsulation. The proposed dynamic ink design offers significant flexibility for 3D bioprinting, and enables straightforward adjustment of the printable formulation to meet application-specific needs
Evidence of the Coulomb force effects in the cross sections of the deuteron-proton breakup at 130 MeV
High precision cross-section data of the deuteron-proton breakup reaction at
130 MeV deuteron energy are compared with the theoretical predictions obtained
with a coupled-channel extension of the CD Bonn potential with virtual
Delta-isobar excitation, without and with inclusion of the long-range Coulomb
force. The Coulomb effect is studied on the basis of the cross-section data
set, extended in this work to about 1500 data points by including breakup
geometries characterized by small polar angles of the two protons. The
experimental data clearly prefer predictions obtained with the Coulomb
interaction included. The strongest effects are observed in regions in which
the relative energy of the two protons is the smallest.Comment: 9 pages, 3 figures, submitted to Physics Letters
Proton tracking in a high-granularity Digital Tracking Calorimeter for proton CT purposes
Radiation therapy with protons as of today utilizes information from x-ray CT
in order to estimate the proton stopping power of the traversed tissue in a
patient. The conversion from x-ray attenuation to proton stopping power in
tissue introduces range uncertainties of the order of 2-3% of the range,
uncertainties that are contributing to an increase of the necessary planning
margins added to the target volume in a patient. Imaging methods and
modalities, such as Dual Energy CT and proton CT, have come into consideration
in the pursuit of obtaining an as good as possible estimate of the proton
stopping power. In this study, a Digital Tracking Calorimeter is benchmarked
for proof-of-concept for proton CT purposes. The Digital Tracking Calorimeteris
applied for reconstruction of the tracks and energies of individual high energy
protons. The presented prototype forms the basis for a proton CT system using a
single technology for tracking and calorimetry. This advantage simplifies the
setup and reduces the cost of a proton CT system assembly, and it is a unique
feature of the Digital Tracking Calorimeter. Data from the AGORFIRM beamline at
KVI-CART in Groningen in the Netherlands and Monte Carlo simulation results are
used to in order to develop a tracking algorithm for the estimation of the
residual ranges of a high number of concurrent proton tracks. The range of the
individual protons can at present be estimated with a resolution of 4%. The
readout system for this prototype is able to handle an effective proton
frequency of 1 MHz by using 500 concurrent proton tracks in each readout frame,
which is at the high end range of present similar prototypes. A future further
optimized prototype will enable a high-speed and more accurate determination of
the ranges of individual protons in a therapeutic beam.Comment: 21 pages, 8 figure
Measurements of scattering observables for the break-up reaction
High-precision measurements of the scattering observables such as cross
sections and analyzing powers for the proton-deuteron elastic and break-up
reactions have been performed at KVI in the last two decades and elsewhere to
investigate various aspects of the three-nucleon force (3NF) effects
simultaneously. In 2006 an experiment was performed to study these effects in
break-up reaction at 135 MeV with the detection system, Big
Instrument for Nuclear polarization Analysis, BINA. BINA covers almost the
entire kinematical phase space of the break-up reaction. The results are
interpreted with the help of state-of-the-art Faddeev calculations and are
partly presented in this contribution.Comment: Proceedings of 19th International IUPAP Conference on Few-Body
Problems in Physics, Bonn University, 31.08 - 05.09.2009, Bonn, GERMAN
Fluorescent Nanodiamonds for Tracking Single Polymer Particles in Cells and Tissues
Polymer nanoparticles are widely used in drug delivery and are also a potential concern due to the increased burden of nano- or microplastics in the environment. In order to use polymer nanoparticles safely and understand their mechanism of action, it is useful to know where within cells and tissues they end up. To this end, we labeled polymer nanoparticles with nanodiamond particles. More specifically, we have embedded nanodiamond particles in the polymer particles and characterized the composites. Compared to conventional fluorescent dyes, these labels have the advantage that nanodiamonds do not bleach or blink, thus allowing long-term imaging and tracking of polymer particles. We have demonstrated this principle both in cells and entire liver tissues.</p
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