A method for converting dose-to-medium to dose-to-tissue in Monte Carlo studies of gold nanoparticle-enhanced radiotherapy

被引:32
作者
Koger, B. [1 ]
Kirkby, C. [1 ,2 ,3 ]
机构
[1] Univ Calgary, Dept Phys & Astron, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Dept Oncol, Calgary, AB T2N 1N4, Canada
[3] Jack Ady Canc Ctr, Dept Med Phys, Lethbridge, AB T1J 1W5, Canada
关键词
gold nanoparticles; Monte Carlo; radiation therapy; RADIATION-THERAPY; SIMULATION; ENERGY; RADIOSENSITIZATION; FEASIBILITY; SPECTRA;
D O I
10.1088/0031-9155/61/5/2014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Gold nanoparticles (GNPs) have shown potential in recent years as a means of therapeutic dose enhancement in radiation therapy. However, a major challenge in moving towards clinical implementation is the exact characterisation of the dose enhancement they provide. Monte Carlo studies attempt to explore this property, but they often face computational limitations when examining macroscopic scenarios. In this study, a method of converting dose from macroscopic simulations, where the medium is defined as a mixture containing both gold and tissue components, to a mean dose-to-tissue on a microscopic scale was established. Monte Carlo simulations were run for both explicitly-modeled GNPs in tissue and a homogeneous mixture of tissue and gold. A dose ratio was obtained for the conversion of dose scored in a mixture medium to dose-to-tissue in each case. Dose ratios varied from 0.69 to 1.04 for photon sources and 0.97 to 1.03 for electron sources. The dose ratio is highly dependent on the source energy as well as GNP diameter and concentration, though this effect is less pronounced for electron sources. By appropriately weighting the monoenergetic dose ratios obtained, the dose ratio for any arbitrary spectrum can be determined. This allows complex scenarios to be modeled accurately without explicitly simulating each individual GNP.
引用
收藏
页码:2014 / 2024
页数:11
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