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首页> 外文期刊>Medical Physics >Experimental determination of beam quality conversion factors k(Q) in clinical photon beams using ferrous sulphate (Fricke) dosimetry.
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Experimental determination of beam quality conversion factors k(Q) in clinical photon beams using ferrous sulphate (Fricke) dosimetry.

机译:使用硫酸亚铁(Fricke)剂量测定法对临床光子束的束质量转换因子k(Q)进行实验测定。

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摘要

The implementation of protocols based on absorbed dose to water standards requires beam quality conversion factors, k(Q). Calculated values of k(Q) are available for ionization chambers used for reference dosimetry. Ideally, k(Q) should be experimentally determined at the same beam qualities as that of the user. In this work we measure k(Q) factors in clinical photon beams and compare them with calculated and measured values. Beam quality conversion factors are determined for clinical photon beams of nominal energies 4 MV, 6 MV, 15 MV, and 25 MV, for commonly used cylindrical ionization chambers. Twelve chambers of eight different types are used. For three of them, no experimental data have previously been available. The experimental procedure is based on measurements with ionization chambers and Fricke dosimetry in the reference beam (60Co gamma radiation) and in clinical linear accelerator beams. The k(Q) values determined in this work generally agree within 0.5% with previously reported experimentalvalues both when %dd(10)x and TPR2010 are used for beam quality specification. The agreement with calculated data is generally within 0.5%, except for the 15 MV beam. For this beam the measured values are usually between 0.5% and 1% lower than the data taken from the TG-51 protocol or the TRS-398 code of practice. For three NE2571 chambers and three NE2581 chambers, the maximum observed deviation of individual k(Q) values is 0.2% and 0.4%, respectively.
机译:基于吸收剂量到水标准的协议的实施需要光束质量转换因子k(Q)。 k(Q)的计算值可用于用于参考剂量测定的电离室。理想情况下,应以与用户相同的光束质量通过实验确定k(Q)。在这项工作中,我们测量临床光子束中的k(Q)因子,并将其与计算值和测量值进行比较。对于常用的圆柱形电离室,确定了标称能量为4 MV,6 MV,15 MV和25 MV的临床光子束的束质量转换因子。使用了八个不同类型的十二个腔室。对于其中三个,以前没有可用的实验数据。实验程序基于在参考光束(60Co伽马射线)和临床线性加速器光束中使用电离室和Fricke剂量法进行的测量。当%dd(10)x和TPR2010用于光束质量规范时,这项工作中确定的k(Q)值通常与先前报道的实验值相差0.5%。除15 MV光束外,与计算数据的一致性通常在0.5%以内。对于此光束,测量值通常比TG-51协议或TRS-398实务守则中的数据低0.5%至1%。对于三个NE2571腔室和三个NE2581腔室,单个k(Q)值的最大观察到的偏差分别为0.2%和0.4%。

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