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SU-E-J-66:用于体内测定质子射程和能量的金基准标记物的质子诱导X射线荧光评估。

SU-E-J-66: Evaluation of Proton Induced X-Ray Fluorescence from Gold Fiducial Markers for In-Vivo Determination of Proton Range and Energy.

作者信息

Tonner Brian, Li Zuofeng, Tishler Derek

机构信息

Moffitt Cancer Center, Tampa, FL.

University of Florida, Jacksonville, FL.

出版信息

Med Phys. 2012 Jun;39(6Part7):3667. doi: 10.1118/1.4734901.

Abstract

PURPOSE

To evaluate a method for in-vivo determination of proton range and post-Bragg peak straggling by detection of proton induced x-ray fluorescence of markers placed at known locations.

METHODS

Therapeutic beams from the UF Proton Therapy Institute were used to excite proton-induced x-ray fluorescence emission (PIXE) from cylindrical pure gold fiducial markers. The markers were embedded in a homogeneous water phantom and PIXE was measured using NaI photodetectors with energy dispersive spectral analysis. The geometry of the phantom and marker placement was chosen to model parallel-opposed beam treatment of prostate cancer by proton therapy. The fluorescence yield from these markers was further modeled using the GEANT4 Monte-Carlo package with low-energy corrections. Gold K and L shell fluorescence yield as determined by the GEANT4 simulations was verified quantitatively by comparison to measured Au yield at energies from 1 MeV to 68 MeV, and to semiempirical model calculations covering the energy range from 1 MeV to 15 MeV.

RESULTS

The Au K-shell fluorescence cross section is significantly smaller thanthat of the L-shell, but the higher yield of the L-shell fluorescence isoffset by the larger absorption as the x-ray exits the phantom. The overallrelative detection efficiency of K and L shell fluorescence depends on thedetails of the shape of the phantom and location of the marker. Acharacteristic shape of fluorescence yield as it depends on proton range isfound, which can be used to extract an in-vivo PDD profile of a spread-outBragg peak (SOBP).

CONCLUSIONS

A combination of a specific protocol for delivering a SOBP, geometriclocation of fiducial markers from CT, and simultaneous detection of protoninduced x-ray fluorescence, can determine the depth range of a primary protonbeam in-vivo. The fluorescence yield as measured at the Proton Therapy Institute is easily distinguished from background radiation.

摘要

目的

通过检测放置在已知位置的标记物的质子诱导X射线荧光,评估一种用于体内测定质子射程和布拉格峰后拖尾的方法。

方法

使用佛罗里达大学质子治疗研究所的治疗束来激发圆柱形纯金基准标记物的质子诱导X射线荧光发射(PIXE)。将标记物嵌入均匀的水体模中,并使用具有能量色散光谱分析的碘化钠光电探测器测量PIXE。选择体模和标记物放置的几何形状来模拟质子治疗对前列腺癌的平行对置束治疗。使用具有低能校正的GEANT4蒙特卡罗软件包进一步模拟这些标记物的荧光产额。通过将GEANT4模拟确定的金K和L壳层荧光产额与1 MeV至68 MeV能量下测得的金产额以及涵盖1 MeV至15 MeV能量范围的半经验模型计算结果进行比较,对其进行了定量验证。

结果

金K壳层荧光截面明显小于L壳层,但当X射线离开体模时,L壳层荧光的较高产额被较大的吸收所抵消。K和L壳层荧光的整体相对检测效率取决于体模形状和标记物位置的细节。发现了一种依赖于质子射程的特征性荧光产额形状,可用于提取扩展布拉格峰(SOBP)的体内百分深度剂量分布。

结论

特定的SOBP输送方案、CT中基准标记物的几何位置以及质子诱导X射线荧光的同时检测相结合,可以确定体内初级质子束的深度范围。在质子治疗研究所测得的荧光产额很容易与背景辐射区分开来。

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