Cherenkov emission has received attention to improve timing resolution of detectors dedicated to positron emission tomography. Since the Cherenkov photons are promptly emitted within an order of 1 ps, the timing performance of the detector would be enhanced compared to a scintillation-based detector. A monolithic Cherenkov radiator which does not emit scintillation photons was employed to suppress reflections in the radiator. However, it is challenging to reconstruct the interaction position of the gamma ray because the number of Cherenkov photons emitted when a gamma ray interacts with the radiator is only 30 at most. As a photodetector, a high-dense photodetector array with individual readout was applied to extract all temporal and spatial information of the Cherenkov photons.
Monolithic Cherenkov radiator
→To maximize the timing performance of Cherenkov emission
Individual readout
→To obtain all temporal- and spatial-information from a few Cherenkov photons
Monte Carlo simulations were performed [Publication 1]. According to the simulations, we found that requirements for the photodetector are high-dense and good single photon time resolution (SPTR).For example, the SPTR must be better than σ = 40 ps to obtain a coincidence time resolution (CTR) of 100 ps full width at half maximum (FWHM).
Moreover, we have investigated potential capability of deep learning to improve the position resolution of the proposed detector [Publication 2].
An experiment measuring the CTR was performed using a high speed photodetector of MCP-PMT (R3809). The SPTR of the MCP-PMT is 25 ps FWHM.
A lead fluoride Cherenkov radiator was attached to the window face plate of the MCP-PMT using an optical glue.
As a result, the CTR better than 50 ps FWHM was successfully obtained, and this result is consistent with the simulation result [Publication 3].
There are optical boundaries in the Cherenkov detector described above. The optical boundaries will worsen the timing performance of the detector. We have developed a Cherenkov-radiator-integrated MCP-PMT (CRI-MCP-PMT) to remove the optical boundaries from the detector. The window face plate of the ordinary MCP-PMT was replaced with the Cherenkov radiator and Al2O3 layer was inserted between the radiator and the photocathode using atomic layer deposition technique.
The CTR was measured using a pair of the CRI-MCP-PMTs, and the CTR of 41.9 ps FWHM was obtained [Publication 4]. Additionally, the CTR was improved to 30.1 ps FWHM by optimizing the analysis parameters, e.g. timing pick-off threshold level and pulse area.
By reviewing all materials starting from scatch and applying an ALD technique, we succeeded in creating ALD-MCPs that ensure low noise and high signal multiplication (gain) without using materials containing lead. Eliminating lead is great step forward because its use is restricted in the RoHS directive issued by the European Union (EU) as a hazardous substance.
A coincidence experiment revealed that a PMT integrating the ALD-MCP can enhance the CTR from 41.9 to 35.4 ps FWHM compared to an ordinary MCP-PMT [reference 6].
We have succeeded in being the first in the world to achieve high-accuracy positron emission imaging without image reconstruction by utilizing the pair of detectors mentioned above, and unique light detection and signal processing techniques [reference 7]. Applying these successful research results are promising to achieve a completely innovative new type of radiation medical imaging system capable of making speedy diagnoses from a simple, compact setup yet with the same or higher accuracy than currently used radiation imaging systems such as positron emission tomography (PET). This will help boost inspection efficiency for detecting diseased tissues or organs, such as from cancer, and also reduce the radiation exposure dose, alleviating the load on the patient and medical staff. We will further improve the detector performance to make this new concept more practical.
1. R. Ota et al., Med. Phys. 45 (2018) pp. 1999-2008
2. F. Hashimoto et al., Biomed. Phys. Eng. Express 5 (2019) 035001
3. R. Ota et al., Nucl. Inst. Meth. A 923 (2019) pp. 1-4
4. R. Ota et al., Phys Med. Biol. 64 (2019) 07LT01
5. R. Ota et al., Phys. Med. biol. 65 (2020) 10NT03
6. R. Ota et al., Phys Med. Biol. 66 (2021) 064006
7. S. I. Kwon, R. Ota, et al., Nat. Photon. 15 (2021) 914-918
US Patent 10,795,035
US Patent 10,816,682
US Patent 10,996,348
US Patent 10,925,557
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