Purpose
Quantitative in vivo molecular imaging of fine brain structures requires highâspatial resolution and highâsensitivity. Positron emission tomography (PET) is an attractive candidate to introduce molecular imaging into standard clinical care due to its highly targeted and versatile imaging capabilities based on the radiotracer being used. However, PET suffers from relatively poor spatial resolution compared to other clinical imaging modalities, which limits its ability to accurately quantify radiotracer uptake in brain regions and nuclei smaller than 3 mm in diameter. Here we introduce a new practical and costâeffective highâresolution and highâsensitivity brainâdedicated PET scanner, using our depthâencoding PrismâPET detector modules arranged in a conformal decagon geometry, to substantially reduce the partial volume effect and enable accurate radiotracer uptake quantification in small subcortical nuclei.
Methods
Two PrismâPET brain scanner setups were proposed based on our 4âtoâ1 and 9âtoâ1 coupling of scintillators to readout pixels using 1.5Ă1.5Ă20$1.5 \times 1.5 \times 20$Â mm3 and 0.987Ă0.987Ă20$0.987 \times 0.987 \times 20$Â mm3 crystal columns, respectively. Monte Carlo simulations of our PrismâPET scanners, Siemens Biograph Vision, and United Imaging EXPLORER were performed using Geant4 application for tomographic emission (GATE). National Electrical Manufacturers Association (NEMA) standard was followed for the evaluation of spatial resolution, sensitivity, and countârate performance. An ultraâmicro hot spot phantom was simulated for assessing image quality. A modified Zubal brain phantom was utilized for radiotracer imaging simulations of 5âHT1A receptors, which are abundant in the raphe nuclei (RN), and norepinephrine transporters, which are highly concentrated in the bilateral locus coeruleus (LC).
Results
The PrismâPET brain scanner with 1.5 mm crystals is superior to that with 1 mm crystals as the former offers better depthâofâinteraction (DOI) resolution, which is key to realizing compact and conformal PET scanner geometries. We achieved uniform 1.3 mm fullâwidthâatâhalfâmaximum (FWHM) spatial resolutions across the entire transaxial fieldâofâview (FOV), a NEMA sensitivity of 52.1 kcps/MBq, and a peak noise equivalent count rate (NECR) of 957.8 kcps at 25.2 kBq/mL using 450â650 keV energy window. Hot spot phantom results demonstrate that our scanner can resolve regions as small as 1.35 mm in diameter at both center and 10 cm away from the center of the transaixal FOV. Both 5âHT1A receptor and norepinephrine transporter brain simulations prove that our PrismâPET scanner enables accurate quantification of radiotracer uptake in small brain regions, with a 1.8âfold and 2.6âfold improvement in the dorsal RN as well as a 3.2âfold and 4.4âfold improvement in the bilateral LC compared to the Biograph Vision and EXPLORER, respectively.
Conclusions
Based on our simulation results, the proposed highâresolution and highâsensitivity PrismâPET brain scanner is a promising costâeffective candidate ...