Geraki K, Farquharson M J, Bradley D A
Department of Radiography, City University, Rutland Place, Charterhouse Square, London EC1M 6PA, UK.
Phys Med Biol. 2004 Jan 7;49(1):99-110. doi: 10.1088/0031-9155/49/1/007.
This paper presents improvements on a previously reported method for the measurement of elements in breast tissue specimens (Geraki et al 2002 Phys. Med. Biol. 47 2327-39). A synchrotron-based system was used for the detection of the x-ray fluorescence (XRF) emitted from iron, copper, zinc and potassium in breast tissue specimens, healthy and cancerous. Calibration models resulting from the irradiation of standard aqueous solutions were used for the quantification of the elements. The present developments concentrate on increasing the convergence between the tissue samples and the calibration models, therefore improving accuracy. For this purpose the composition of the samples in terms of adipose and fibrous tissue was evaluated, using an energy dispersive x-ray diffraction (EDXRD) system. The relationships between the attenuation and scatter properties of the two tissue components and water were determined through Monte Carlo simulations. The results from the simulations and the EDXRD measurements allowed the XRF data from each specimen to be corrected according to its composition. The statistical analysis of the elemental concentrations of the different groups of specimens reveals that all four elements are found in elevated levels in the tumour specimens. The increase is less pronounced for iron and copper and most for potassium and zinc. Other observed features include the substantial degree of inhomogeneity of elemental distributions within the volume of the specimens, varying between 4% and 36% of the mean, depending on the element and the type of the sample. The accuracy of the technique, based on the measurement of a standard reference material, proved to be between 3% and 22% depending on the element, which presents only a marginal improvement (1%-3%) compared to the accuracy of the previously reported results. The measurement precision was between 1% and 9% while the calculated uncertainties on the final elemental concentrations ranged between 10% and 16%.
本文介绍了对先前报道的乳腺组织标本中元素测量方法(Geraki等人,2002年,《物理医学与生物学》47卷,2327 - 39页)的改进。使用基于同步加速器的系统来检测健康和癌变乳腺组织标本中铁、铜、锌和钾发出的x射线荧光(XRF)。由标准水溶液辐照产生的校准模型用于元素的定量分析。目前的进展集中在提高组织样本与校准模型之间的一致性,从而提高准确性。为此,使用能量色散x射线衍射(EDXRD)系统评估样本中脂肪组织和纤维组织的组成。通过蒙特卡罗模拟确定了两种组织成分和水的衰减与散射特性之间的关系。模拟结果和EDXRD测量结果使每个标本的XRF数据能够根据其组成进行校正。对不同组标本元素浓度的统计分析表明,在肿瘤标本中所有四种元素的含量都有所升高。铁和铜的升高不太明显,而钾和锌的升高最为明显。其他观察到的特征包括标本体积内元素分布的显著不均匀程度,根据元素和样本类型的不同,在平均值的4%至36%之间变化。基于标准参考物质测量的该技术的准确度,根据元素的不同,在3%至22%之间,与先前报道结果的准确度相比,仅略有提高(1% - 3%)。测量精度在1%至9%之间,而最终元素浓度的计算不确定度在10%至16%之间。