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Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence

Synchrotron-generated microbeam radiotherapy holds great promise for future treatment, but the high dose gradients present conventional dosimetry with a challenge. Measuring the important peak-to-valley dose ratio (PVDR) of a microbeam-collimated synchrotron source requires both a dosimeter and an a...

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Autores principales: Annabell, N., Yagi, N., Umetani, K., Wong, C., Geso, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621279/
https://www.ncbi.nlm.nih.gov/pubmed/22514166
http://dx.doi.org/10.1107/S0909049512005237
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author Annabell, N.
Yagi, N.
Umetani, K.
Wong, C.
Geso, M.
author_facet Annabell, N.
Yagi, N.
Umetani, K.
Wong, C.
Geso, M.
author_sort Annabell, N.
collection PubMed
description Synchrotron-generated microbeam radiotherapy holds great promise for future treatment, but the high dose gradients present conventional dosimetry with a challenge. Measuring the important peak-to-valley dose ratio (PVDR) of a microbeam-collimated synchrotron source requires both a dosimeter and an analysis method capable of exceptional spatial resolution. The PVDR is of great interest since it is the limiting factor for potential application of the microbeam radiation therapy technique clinically for its tissue-sparing properties (i.e. the valley dose should be below the tolerance of normal tissue). In this work a new method of measuring the dose response of PRESAGE dosimeters is introduced using the fluorescence from a 638 nm laser on a confocal laser-scanning microscope. This fluorescent microscopy method produces dosimetry data at a pixel size as low as 78 nm, giving a much better spatial resolution than optical computed tomography, which is normally used for scanning PRESAGE dosimeters. Using this technique the PVDR of the BL28B2 microbeam at the SPring-8 synchrotron in Japan is estimated to be approximately 52:1 at a depth of 2.5 mm. The PVDR was also estimated with EBT2 GAFchromic films as 30.5:1 at the surface in order to compare the PRESAGE fluorescent results with a more established dosimetry system. This estimation is in good agreement with previously measured ratios using other dosimeters and Monte Carlo simulations. This means that it is possible to use PRESAGE dosimeters with confocal microscopy for the determination of PVDR.
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spelling pubmed-36212792013-04-12 Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence Annabell, N. Yagi, N. Umetani, K. Wong, C. Geso, M. J Synchrotron Radiat Research Papers Synchrotron-generated microbeam radiotherapy holds great promise for future treatment, but the high dose gradients present conventional dosimetry with a challenge. Measuring the important peak-to-valley dose ratio (PVDR) of a microbeam-collimated synchrotron source requires both a dosimeter and an analysis method capable of exceptional spatial resolution. The PVDR is of great interest since it is the limiting factor for potential application of the microbeam radiation therapy technique clinically for its tissue-sparing properties (i.e. the valley dose should be below the tolerance of normal tissue). In this work a new method of measuring the dose response of PRESAGE dosimeters is introduced using the fluorescence from a 638 nm laser on a confocal laser-scanning microscope. This fluorescent microscopy method produces dosimetry data at a pixel size as low as 78 nm, giving a much better spatial resolution than optical computed tomography, which is normally used for scanning PRESAGE dosimeters. Using this technique the PVDR of the BL28B2 microbeam at the SPring-8 synchrotron in Japan is estimated to be approximately 52:1 at a depth of 2.5 mm. The PVDR was also estimated with EBT2 GAFchromic films as 30.5:1 at the surface in order to compare the PRESAGE fluorescent results with a more established dosimetry system. This estimation is in good agreement with previously measured ratios using other dosimeters and Monte Carlo simulations. This means that it is possible to use PRESAGE dosimeters with confocal microscopy for the determination of PVDR. International Union of Crystallography 2012-03-15 /pmc/articles/PMC3621279/ /pubmed/22514166 http://dx.doi.org/10.1107/S0909049512005237 Text en © N. Annabell et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Papers
Annabell, N.
Yagi, N.
Umetani, K.
Wong, C.
Geso, M.
Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title_full Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title_fullStr Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title_full_unstemmed Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title_short Evaluating the peak-to-valley dose ratio of synchrotron microbeams using PRESAGE fluorescence
title_sort evaluating the peak-to-valley dose ratio of synchrotron microbeams using presage fluorescence
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621279/
https://www.ncbi.nlm.nih.gov/pubmed/22514166
http://dx.doi.org/10.1107/S0909049512005237
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