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Repeated imaging of lung cancer development using PIXSCAN, a low dose micro-CT scanner based on XPAD hybrid pixel detectors

Authors :
C. Hemmer
J. C. Clemens
Franca Cassol Brunner
P. Breugnon
Geneviève Rougon
F. Mann
A. Bonissent
P. Delpierre
B. Dinkespiler
E. Vigeolas
C. Meessen
J. Luchino
Christian Morel
Franck Debarbieux
Centre de Physique des Particules de Marseille (CPPM)
Aix Marseille Université (AMU)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)
Institut de Biologie du Développement de Marseille (IBDM)
Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
Source :
IEEE Transactions on Nuclear Science, World Molecular Imaging Congress 2008, World Molecular Imaging Congress 2008, Sep 2008, Nice, France. pp.242-245, ⟨10.1109/TNS.2009.2037319⟩, IEEE Transactions on Nuclear Science, Institute of Electrical and Electronics Engineers, 2010, 57, pp.242-245, HAL, IEEE Transactions on Nuclear Science, 2010, 57, pp.242-245. ⟨10.1109/TNS.2009.2037319⟩, Nucl. Sci., Nucl. Sci., 2010, 57, pp.242-245
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

International audience; PIXSCAN is the first micro-CT prototype based on XPAD hybrid pixel detectors whose properties (high signal to noise ratio and high detection efficiency) allow imaging at low irradiation dose. We have tested the impact of repeated imaging sessions with PIXSCAN on living mice. Mice were subjected on average to 10 imaging sessions over two weeks without any detectable sign of X-ray injuries as assessed by spontaneous activity in the cage, examination of hair and skin, or comparison of lung absorbing properties for X-rays. PIXSCAN was therefore used to non-invasively monitor the progression of lung metastasis in a murine model of cancer. Aim of was two-fold: i) to provide imaging assistance to decide timing of animal sacrifice and subsequent histological characterization of the tumors; ii) to optimize imaging protocol to allow direct evaluation of new therapeutic agents to stop cancer progression. Comparing in vivo tomographic reconstruction of freely breathing mice with post mortem examination of their lungs, we have shown that identification and localization of millimetric tumors was compatible with our low dose X-ray imaging protocol, allowing determination of tumor growth kinetics. In this context, interest of respiratory gating will be discussed.

Details

Language :
English
ISSN :
00189499
Database :
OpenAIRE
Journal :
IEEE Transactions on Nuclear Science, World Molecular Imaging Congress 2008, World Molecular Imaging Congress 2008, Sep 2008, Nice, France. pp.242-245, ⟨10.1109/TNS.2009.2037319⟩, IEEE Transactions on Nuclear Science, Institute of Electrical and Electronics Engineers, 2010, 57, pp.242-245, HAL, IEEE Transactions on Nuclear Science, 2010, 57, pp.242-245. ⟨10.1109/TNS.2009.2037319⟩, Nucl. Sci., Nucl. Sci., 2010, 57, pp.242-245
Accession number :
edsair.doi.dedup.....d16f3d4c9fe95100bafc875d574a47e6
Full Text :
https://doi.org/10.1109/TNS.2009.2037319⟩