The innovative 52gMn for PET imaging: production cross section modeling and dosimetric evaluation
Abstract
Background: Recently, the reaction natV(α,x)52gMn has been proposed as a possible alternative to the standard natCr(p,x)52gMn one, but improvements in the modeling were needed to better compare the two production routes. Purpose: This work focuses on the development of precise simulations and models to compare the 52gMn production from both reactions in terms of amount of activity and radionuclidic purity (RNP), as well as in terms of dose increase (DI) due to the co-produced radioactive contaminants, with respect to a pure 52gMnCl2 injection. Methods: The nuclear code Talys has been employed to optimize the natV(α,x)52gMn cross section by tuning the parameters of the microscopic level densities. Dosimetric assessments of [xxMn]Cl2 have been accomplished with OLINDA software 2.2.0 using female and male phantoms. At the end, the yield of xxMn radioisotopes estimated for the two production routes have been combined with the dosimetric results, to assess the DI at different times after the end of the irradiation. Results: Good agreement was obtained between cross sections calculations and measurements. The comparison of the two reaction channels suggests that natV(α,x)52gMn leads to higher yield and higher purity, resulting in a less harmful impact on patients' health in terms of DI. Conclusions: Both natV(α,x) and natCr(p,x) production routes provide clinically acceptable 52gMnCl2 for PET imaging. However, the natV(α,x)52gMn reaction provides a DI systematically lower than the one obtainable with natCr(p,x)52gMn and a longer time window in which it can be used clinically (RNP 99\%).
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