Abstract

BackgroundWhile alpha microdosimetry dates back a couple of decades, the effects of localized energy deposition of alpha particles are often still unclear since few comparative studies have been performed. Most modern alpha microdosimetry studies rely for large parts on simulations, which negatively impacts both the simplicity of the calculations and the reliability of the results. A novel microdosimetry method based on the Fluorescent Nuclear Track Detector, a versatile tool that can measure individual alpha particles at sub-micron resolution, yielding accurate energy, fluence and dose rate measurements, was introduced to address these issues.MethodsBoth the detectors and U87 glioblastoma cell cultures were irradiated using an external Am241 alpha source. The alpha particle tracks measured with a Fluorescent Nuclear Track Detector were used together with high resolution 3D cell geometries images to calculate the nucleus dose distribution in the U87 glioblastoma cells. The experimentally obtained microdosimetry parameters were thereafter applied to simulations of 3D U87 cells cultures (spheroids) with various spatial distributions of isotopes to evaluate the effect of the nucleus dose distribution on the expected cell survival.ResultsThe new experimental method showed good agreement with the analytically derived nucleus dose distributions. Small differences (< 5%) in the relative effectiveness were found for isotopes in the cytoplasm and on the cell membrane versus external irradiation, while isotopes located in the nucleus or on the nuclear membrane showed a substantial increase in relative effectiveness (33 – 51%).ConclusionsThe ease-of-use, good accuracy and use of experimentally derived characteristics of the radiation field make this method superior to conventional simulation-based microdosimetry studies. Considering the uncertainties found in alpha radionuclide carriers in-vivo and in-vitro, together with the large contributions from the relative biological effectiveness and the oxygen enhancement ratio, it is expected that only carriers penetrating or surrounding the cell nucleus will substantially benefit from microdosimetry.

Highlights

  • While alpha microdosimetry dates back a couple of decades, the effects of localized energy deposition of alpha particles are often still unclear since few comparative studies have been performed

  • The interest in alpha radionuclide therapy remains on the rise [1,2,3,4,5], partly for its ability to deal with tumours resistant to gamma and beta radiation attributed to the high Linear Energy Transfer (LET) of alpha particles [6, 7]

  • Microdosimetry for alpha particles deals with the determination of the absorbed dose distribution in cell nuclei, the so called nucleus dose distribution (NDD) [8]

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Summary

Introduction

While alpha microdosimetry dates back a couple of decades, the effects of localized energy deposition of alpha particles are often still unclear since few comparative studies have been performed. (FNTD) [15, 16], which allows for robust measurement of individual alpha particles with great accuracy [17, 18] Using these detectors, the point of entrance, direction and energy of alpha particles tracks can be measured at submicrometer resolution [19, 20]. The point of entrance, direction and energy of alpha particles tracks can be measured at submicrometer resolution [19, 20] This detailed knowledge of the radiation field can be used to calculate the energy deposited in cell nuclei with relative ease and without the need for assumptions regarding the radiation field characteristics or geometry. The resulting microdosimetric spectra can be of great value for both cell survival studies as well as DNA damage and repair studies

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