9–12 May 2006
Palais du Pharo, Marseille
Europe/Zurich timezone

Preliminary Report on LabPET, a High-Performance APD-Based Digital PET Scanner for Small Animal Imaging

11 May 2006, 14:00
1h
Palais du Pharo, Marseille

Palais du Pharo, Marseille

Speaker

Prof. Roger LECOMTE (Université de Sherbrooke, Nuclear Medicine & Radiobiology)

Description

LabPET is a second-generation APD-based PET scanner featuring quasi-individual crystal readout and massively parallel digital processing with advanced signal analysis heuristics for high-performance in vivo molecular imaging of small animals. The system implements several unique features to enhance throughput and facilitate complex imaging protocols in live animals. The basic LabPET system consists of 3072 2x2x10 mm³ scintillators assembled into phoswich LYSO/LGSO pairs, each read out by an avalanche photodiode. The detectors are arranged into 16 rings of 192 crystals each, having 16.2 cm in diameter by 37.5 mm axially. The 16 rings allow for acquisition of 31 effective image slices extending up to 110 mm in diameter. The dual-crystal readout scheme avoids resolution degradation due to light- or charge-sharing and enables very high singles count rates with low dead time in the detector front-end. Advanced parallel digital signal processing and analysis algorithms are implemented in high-performance programmable devices for crystal identification, energy discrimination and time stamping of events from individual pixels. Virtually error-free crystal identification is achieved using an auto-regressive least-mean square moving average method. Coincidence events are sorted in real time and recorded in list mode, together with scanner status information and animal physiological data. The measured intrinsic spatial resolution of coincidence response functions is 1.2 mm FWHM and 2.3 mm FWTM both axially and radially, with a near triangular shape confirming the excellent resolving capability of APD detector arrays. Using a simple linear interpolation algorithm, preliminary time resolutions of 4.5, 7.5 and 9.6 ns FWHM were obtained for LYSO-LYSO, LYSO-LGSO and LGSO-LGSO coincidences, respectively. These resolutions will be improved by implementing digital constant fraction or artificial neural networks algorithms. Initial images with a resolution phantom show that 1.2 mm hot rods can be clearly resolved. The scanner is fully integrated with ancillary devices (injectors, life-sign monitors, blood counter, etc.), all controlled through a centralized user-interface, allowing a single operator to perform elaborate imaging protocols with maximum flexibility and efficiency. The system was designed to provide a fully integrated solution for performing the most demanding molecular imaging investigations with increased throughput in a busy research environment.

Authors

Mr François BÉLANGER (Université de Sherbrooke, Electrical & Computer Engineering) Mr Jules CADORETTE (CHUS/CRCÉL, Sherbrooke Molecular Imaging Centre) Mr Marc-André TÉTRAULT (Université de Sherbrooke, Electrical & Computer Engineering) Mr Martin D. LEPAGE (Advanced Molecular Imaging (AMI) Inc.) Mr Nicolas VISCOGLIOSI (Université de Sherbrooke, Electrical & Computer Engineering) Prof. Roger LECOMTE (Université de Sherbrooke, Nuclear Medicine & Radiobiology) Prof. Réjean FONTAINE (Université de Sherbrooke, Electrical & Computer Engineering) Dr Vitali SELIVANOV (Advanced Molecular Imaging (AMI) Inc.)

Co-authors

Mr François LEMIEUX (Université de Sherbrooke, Electrical & Computer Engineering) Mr Ghislain ROBERT (Advanced Molecular Imaging (AMI) Inc.) Mr Hicham SEMMAOUI (Université de Sherbrooke, Electrical & Computer Engineering) Mr Marc-Antoine LEMONDE (Université de Sherbrooke, Physics) Ms Mélanie BERGERON (Université de Sherbrooke, Physics)

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