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A preclinical microbeam facility with a conventional x‐ray tube

PURPOSE: Microbeam radiation therapy is an innovative treatment approach in radiation therapy that uses arrays of a few tens of micrometer wide and a few hundreds of micrometer spaced planar x‐ray beams as treatment fields. In preclinical studies these fields efficiently eradicated tumors while norm...

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Autores principales: Bartzsch, Stefan, Cummings, Craig, Eismann, Stephan, Oelfke, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association of Physicists in Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5965367/
https://www.ncbi.nlm.nih.gov/pubmed/27908159
http://dx.doi.org/10.1118/1.4966032
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author Bartzsch, Stefan
Cummings, Craig
Eismann, Stephan
Oelfke, Uwe
author_facet Bartzsch, Stefan
Cummings, Craig
Eismann, Stephan
Oelfke, Uwe
author_sort Bartzsch, Stefan
collection PubMed
description PURPOSE: Microbeam radiation therapy is an innovative treatment approach in radiation therapy that uses arrays of a few tens of micrometer wide and a few hundreds of micrometer spaced planar x‐ray beams as treatment fields. In preclinical studies these fields efficiently eradicated tumors while normal tissue could effectively be spared. However, development and clinical application of microbeam radiation therapy is impeded by a lack of suitable small scale sources. Until now, only large synchrotrons provide appropriate beam properties for the production of microbeams. METHODS: In this work, a conventional x‐ray tube with a small focal spot and a specially designed collimator are used to produce microbeams for preclinical research. The applicability of the developed source is demonstrated in a pilot in vitro experiment. The properties of the produced radiation field are characterized by radiochromic film dosimetry. RESULTS: 50 μm wide and 400 μm spaced microbeams were produced in a 20 × 20 mm(2) sized microbeam field. The peak to valley dose ratio ranged from 15.5 to 30, which is comparable to values obtained at synchrotrons. A dose rate of up to 300 mGy/s was achieved in the microbeam peaks. Analysis of DNA double strand repair and cell cycle distribution after in vitro exposures of pancreatic cancer cells (Panc1) at the x‐ray tube and the European Synchrotron leads to similar results. In particular, a reduced G2 cell cycle arrest is observed in cells in the microbeam peak region. CONCLUSIONS: At its current stage, the source is restricted to in vitro applications. However, moderate modifications of the setup may soon allow in vivo research in mice and rats.
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spelling pubmed-59653672018-05-24 A preclinical microbeam facility with a conventional x‐ray tube Bartzsch, Stefan Cummings, Craig Eismann, Stephan Oelfke, Uwe Med Phys Emerging Imaging and Therapy Modalities PURPOSE: Microbeam radiation therapy is an innovative treatment approach in radiation therapy that uses arrays of a few tens of micrometer wide and a few hundreds of micrometer spaced planar x‐ray beams as treatment fields. In preclinical studies these fields efficiently eradicated tumors while normal tissue could effectively be spared. However, development and clinical application of microbeam radiation therapy is impeded by a lack of suitable small scale sources. Until now, only large synchrotrons provide appropriate beam properties for the production of microbeams. METHODS: In this work, a conventional x‐ray tube with a small focal spot and a specially designed collimator are used to produce microbeams for preclinical research. The applicability of the developed source is demonstrated in a pilot in vitro experiment. The properties of the produced radiation field are characterized by radiochromic film dosimetry. RESULTS: 50 μm wide and 400 μm spaced microbeams were produced in a 20 × 20 mm(2) sized microbeam field. The peak to valley dose ratio ranged from 15.5 to 30, which is comparable to values obtained at synchrotrons. A dose rate of up to 300 mGy/s was achieved in the microbeam peaks. Analysis of DNA double strand repair and cell cycle distribution after in vitro exposures of pancreatic cancer cells (Panc1) at the x‐ray tube and the European Synchrotron leads to similar results. In particular, a reduced G2 cell cycle arrest is observed in cells in the microbeam peak region. CONCLUSIONS: At its current stage, the source is restricted to in vitro applications. However, moderate modifications of the setup may soon allow in vivo research in mice and rats. American Association of Physicists in Medicine 2016-11-02 2016-12 /pmc/articles/PMC5965367/ /pubmed/27908159 http://dx.doi.org/10.1118/1.4966032 Text en © 2016 The Authors. Published by American Association of Physicists in Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Emerging Imaging and Therapy Modalities
Bartzsch, Stefan
Cummings, Craig
Eismann, Stephan
Oelfke, Uwe
A preclinical microbeam facility with a conventional x‐ray tube
title A preclinical microbeam facility with a conventional x‐ray tube
title_full A preclinical microbeam facility with a conventional x‐ray tube
title_fullStr A preclinical microbeam facility with a conventional x‐ray tube
title_full_unstemmed A preclinical microbeam facility with a conventional x‐ray tube
title_short A preclinical microbeam facility with a conventional x‐ray tube
title_sort preclinical microbeam facility with a conventional x‐ray tube
topic Emerging Imaging and Therapy Modalities
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5965367/
https://www.ncbi.nlm.nih.gov/pubmed/27908159
http://dx.doi.org/10.1118/1.4966032
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