Initial Measurements with the PETsys TOFPET2 ASIC Evaluation Kit and a Characterization of the ASIC TDC

For a first characterization, we used the two KETEK-PM3325-WB SiPMs each equipped with a 3x3x5 mm${}^3$ LYSO scintillation crystal provided with the PETsys TOFPET2 ASIC Evaluation Kit. We changed the lower of two discriminator thresholds (D_T1) in the timing branch from vth_t1 = 5 - 30. The overvoltage was varied in a range of 1.25 V - 7.25 V. The ambient temperature was kept at 16{\deg}C. For all measurements, we performed an energy calibration including a correction for saturation. We evaluated the energy resolution, the coincidence resolving time (CRT) and the coincidence rate. At an overvoltage of 6 V, we obtained an energy resolution of about 10% FWHM, a CRT of approximately 210 ps FWHM and 400 ps FWTM, the coincidence rate showed only small variations of about 5%. To investigate the influence of the ambient temperature, it was varied between 12{\deg}C - 20{\deg}C. At 12{\deg}C and an overvoltage of 6.5 V, a CRT of approx. 195 ps FWHM and an energy resolution of about 9.5% FWHM could be measured. Observed satellite peaks in the time difference spectra were investigated in more detail. We could show that the location of the satellite peaks is correlated with a programmable delay element in the trigger circuit.Comment: This paper is under review with IEEE TRPMS. It has been presented in a talk at the PSMR 2018. This version of the manuscript was submitted as revision 2 to TRPMS after incrporating the comments of the reviewers. Only minor textchanges were made. Results, values and figures did not chang

Advances in Clinical Molecular Imaging Instrumentation

In this article, we describe recent developments in the design of both single-photon emission computed tomography (SPECT) and positron emission tomography (PET) instrumentation that have led to the current range of superior performance instruments. The adoption of solid-state technology for either complete detectors [e.g., cadmium zinc telluride (CZT)] or read-out systems that replace photomultiplier tubes [avalanche photodiodes (APD) or silicon photomultipliers (SiPM)] provide the advantage of compact technology, enabling flexible system design. In SPECT, CZT is well suited to multi-radionuclide and kinetic studies. For PET, SiPM technology provides MR compatibility and superior time-of-flight resolution, resulting in improved signal-to-noise ratio. Similar SiPM technology has also been used in the construction of the first SPECT insert for clinical brain SPECT/MRI

The future of hybrid imaging—part 3: PET/MR, small-animal imaging and beyond

Since the 1990s, hybrid imaging by means of software and hardware image fusion alike allows the intrinsic combination of functional and anatomical image information. This review summarises in three parts the state of the art of dual-technique imaging with a focus on clinical applications. We will attempt to highlight selected areas of potential improvement of combined imaging technologies and new applications. In this third part, we discuss briefly the origins of combined positron emission tomography (PET)/magnetic resonance imaging (MRI). Unlike PET/computed tomography (CT), PET/MRI started out from developments in small-animal imaging technology, and, therefore, we add a section on advances in dual- and multi-modality imaging technology for small animals. Finally, we highlight a number of important aspects beyond technology that should be addressed for a sustained future of hybrid imaging. In short, we predict that, within 10 years, we may see all existing multi-modality imaging systems in clinical routine, including PET/MRI. Despite the current lack of clinical evidence, integrated PET/MRI may become particularly important and clinically useful in improved therapy planning for neurodegenerative diseases and subsequent response assessment, as well as in complementary loco-regional oncology imaging. Although desirable, other combinations of imaging systems, such as single-photon emission computed tomography (SPECT)/MRI may be anticipated, but will first need to go through the process of viable clinical prototyping. In the interim, a combination of PET and ultrasound may become available. As exciting as these new possible triple-technique—imaging systems sound, we need to be aware that they have to be technologically feasible, applicable in clinical routine and cost-effective

Organ-Dedicated Molecular Imaging Systems

[EN] In this review, we will cover both clinical and technical aspects of the advantages and disadvantages of organ specific (dedicated) molecular imaging (MI) systems, namely positron emission tomography (PET) and single photon emission computed tomography, including gamma cameras. This review will start with the introduction to the organ-dedicated MI systems. Thereafter, we will describe the differences and their advantages/disadvantages when compared with the standard large size scanners. We will review time evolution of dedicated systems, from first attempts to current scanners, and the ones that ended in clinical use. We will review later the state of the art of these systems for different organs, namely: breast, brain, heart, and prostate. We will also present the advantages offered by these systems as a function of the special application or field, such as in surgery, therapy assistance and assessment, etc. Their technological evolution will be introduced for each organ-based imager. Some of the advantages of dedicated devices are: higher sensitivity by placing the detectors closer to the organ, improved spatial resolution, better image contrast recovery (by reducing the noise from other organs), and also lower cost. Designing a complete ring-shaped dedicated PET scanner is sometimes difficult and limited angle tomography systems are preferable as they have more flexibility in placing the detectors around the body/organ. Examples of these geometries will be presented for breast, prostate and heart imaging. Recently achievable excellent time of flight capabilities below 300-ps full width at half of the maximum reduce significantly the impact of missing angles on the reconstructed images.This work was supported in part by the European Research Council through the European Union's Horizon 2020 Research and Innovation Program under Grant 695536, in part by the EU through the FP7 Program under Grant 603002, and in part by the Spanish Ministerio de Economia, Industria y Competitividad through PROSPET (DTS15/00152) funded by the Ministerio de Economia y Competitividad under Grant TEC2016-79884-C2-1-R.González Martínez, AJ.; Sánchez, F.; Benlloch Baviera, JM. (2018). Organ-Dedicated Molecular Imaging Systems. IEEE Transactions on Radiation and Plasma Medical Sciences. 2(5):388-403. https://doi.org/10.1109/TRPMS.2018.2846745S3884032