A brain PET insert MR compatible: Final design and first results

A whole-body PET device is sometimes not suitable for brain studies because the achieved image resolution is typically not sufficient to investigate small size structures. Thus, a dedicated brain PET insert system with high performance would overcome such limitations. Moreover, these functional studies lack of anatomical information. It is shown elsewhere the convenience of simultaneously acquisition of PET and MR data. In this work we show the final design and first pilot evaluation tests of a novel brain PET insert. Each detector block is based on a monolithic scintillation crystal, an array of SiPMs and a readout allowing characterizing the scintillation light distribution in the X and Y detector axes. The scintillators have a parallelepiped geometry with dimensions of 50×50×20 mm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sup> . Their lateral walls are black painted and with the entrance face coupled to a retroreflector optical layer. We have determined an average (XYZ) detector spatial resolution through the FWHM of 1.2 mm (whole scintillator volume). The DOI resolution was measured with lateral incidence experiments and found to be about 3.5 mm, also on average for all photons depth of interactions and crystal positions. Thanks to the retroreflector, the energy resolution improves when compared to a case with all surfaces black painted, resulting on an average value of 13%. The tomographic reconstruction of the data was evaluated using different algorithms, including analytical (FBP STIR-3D), iterative (MLEM and List Mode OS) and a novel method that provides images by directly tracing the measured LORs. The minimum pixel/voxel sizes that were tried are 0.8/0.4 mm, 1.0/0.5 mm and 0.16/0.16 mm, respectively. All methods made it possible to show the PET system capabilities to resolve 1.6 mm rods in a Derenzo-like phantom filled with 150 uCi and scanned for 20 minutes. Pilot tests of the PET insert inside a clinical 3T MR showed a good system performance for most of the sequences typically used for brain imaging.