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CELLION Technical Report
Tilman Butz Universität Leipzig CELLION Midterm Meeting Bordeaux 3.2.–
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Map of Sites
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Table of Contents Introduction
Components of NMPs with external beams Accelerators and ion sources Horizontal vs. vertical beamlines Beam formation Exit windows Ion detectors and online microscopy Petri dishes Target translation stages Hit accuracy Automatic cell recognition Track visualization Summary
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Cell to cell communication !
Introduction Random irradiation superposition of various interaction points => mixture of cellular responses Targeted irradiation selected interaction point counted number of ions => specific cellular responses Cell to cell communication !
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Accelerators and Ion Sources
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Linear Energy Transfer
A. Hauptner, S. Dietzel, G.A. Drexler, P. Reichart, R. Krücken, T. Cremer, A.A. Friedl, G. Dollinger, Radiat. Environ. Biophys 42 (2004) 237.
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2 MV Tandetron at Guildford
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intermediate image distance
A high demagnification system for the sub-micron region 5000 3150 100 40 250 object image Dimensions in mm. Not to scale. a0 =7.5 300 beam axis cross-over X intermediate image distance working distance -A B C -D -C A long working distance quadrupole doublet – triplet setup for 3 MeV protons allowing : High demagnifications (65 X 100) keeping spherical aberrations at a reasonable level. Intermediate beam focus and cross over for real imaging, diagnostics and fine tuning of the doublet Comfortable intermediate (300 mm) and working distances (250 mm) in analysis or cellular irradiation configuration A total beam length less than 10 metres 100 mm long OM 50 quadrupoles from Oxford Microbeams Ltd., U.K. (bore gap : 15 mm) Centre d’Etudes Nucléaires de Bordeaux-Gradignan
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Horizontal vs. vertical beam lines
Microbeam room 4MV Van de Graaff Gray Cancer Institute, London
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Horizontal vs. vertical beam lines
LIPSION, Leipzig
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Horizontal vs. vertical Petri dishes
medium residual medium for vertical beams for horizontal beams
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Beam Formation: Collimation
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Beam Formation: Collimation
Legnaro
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Beam Formation: Focusing
Scanner magnetic lens system object slits aperture slits beam focus Microprobe beam line at LIPSION, Leipzig
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Exit Windows
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Exit Windows scanner exit window
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Proton Beam in Air
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External Beam Line Properties
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Ion Detectors and On-line Microscopy
CCD camera + intensifier optical table collimator assembly stage stage support & Z drive light source objective support and alignment GCI, London
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Ion Detectors and On-line Microscopy
GCI, London
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Single Ion Transmission Detector
GSI, Darmstadt IFJ, Kraków (Kraków plans to install a gas proportional counter like RARAF) e- secondary electrons from exit window allow single ion detection with nearly 100% efficiency Channeltron
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Petri Dish GCI, London
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Petri Dish Petri dishes used in Leipzig and Kraków LIPSION, Leipzig
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(polypropylene 4 µm + Cell-Tack)
Petri Dish BACK FRONT 1 cm Polymer culture support layer (polypropylene 4 µm + Cell-Tack) glass window CENBG, Bordeaux
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Translation Stage fast translation stage using voice coils
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Hit Accuracy Endothelial cell LIPSION, Leipzig
with nucleus of about 15 µm × 10 µm LIPSION, Leipzig
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Automatic Cell Recognition
CCD camera cell finding & positioning microscope computer control shutter stage detector particle microbeam GCI, London
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Automatic Cell Recognition
Carbon 4.8MeV/u; 5 hits, 3µm distance GSI, Darmstadt Recognised cell nuclei marked by crosses. Red cross: nucleus selected for irradiation
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Automatic Cell Recognition Work in Kraków
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Track Visualization: Foci
patterned irradiation 10 µm targeted irradiation
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Summary Nuclear microprobes are state of the art tools to deliver a counted number of ions to cellular targets with micron and sub-micron precision. All state of the art detection schemes for the cellular response have to be applied in order to study low dose biological effects in detail. The rapid growth of the European nuclear microprobe community with radiobiological programs is encouraging and parallels worldwide efforts.
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