The application of the distance histogram in microdosimetry for evaluating heterogeneity

Heterogeneity of radionuclide distributions at a microscopic level is relevant for the dosimetry of short path-length emissions. The present study explores the methodological aspects and the limitations of source target histograms by using computer simulations of radionuclide distributions. Sources were formed by labeled cells, containing 50 decay sites each. Cell nuclei were considered as targets. Within a matrix of 2,500 cells, the authors investigated uniform distributions (MIRD assumption), various cluster sizes, the single labeled cell, and a random distribution. Furthermore, four different intracellular source localizations were studied in a matrix of one cell. The distance histograms for both matrices were combined. For both 125I and 131I , absorbed doses in the targets were calculated from multiplication of the distance histograms by the point source absorbed radiation dose distribution. The presented results indicate that the use of distance histograms might be a mathematically convenient approach to microdosimetrical studies. They provide a means to study combinations of source distributions at various levels of magnification for several radionuclides within a reasonable calculation time