Institute of Analytical and Bioanalytical Chemistry, Ulm University, 89081, Ulm, Germany.
Institute of Comparative Molecular Endocrinology, Ulm University, 89081, Ulm, Germany.
Anal Bioanal Chem. 2020 Sep;412(24):6419-6429. doi: 10.1007/s00216-020-02614-8. Epub 2020 Apr 26.
Trace elements are essential for life and their concentration in cells and tissues must be tightly maintained and controlled to avoid pathological conditions. Established methods to measure the concentration of trace elements in biological matrices often provide only single element information, are time-consuming, and require special sample preparation. Therefore, the development of straightforward and rapid analytical methods for enhanced, multi-trace element determination in biological samples is an important and raising field of trace element analysis. Herein, we report on the development and validation of a reliable method based on total reflection X-ray fluorescence (TXRF) analysis to precisely quantify iron and other trace metals in a variety of biological samples, such as the liver, parenchymal and non-parenchymal liver cells, and bone marrow-derived macrophages. We show that TXRF allows fast and simple one-point calibration by addition of an internal standard and has the potential of multi-element analysis in minute sample amounts. The method was validated for iron by recovery experiments in homogenates in a wide concentration range from 1 to 1600 μg/L applying well-established graphite furnace atomic absorption spectrometry (GFAAS) as a reference method. The recovery rate of 99.93 ± 0.14% reveals the absence of systematic errors. Furthermore, the standard reference material "bovine liver" (SRM 1577c, NIST) was investigated in order to validate the method for further biometals. Quantitative recoveries (92-106%) of copper, iron, zinc, and manganese prove the suitability of the developed method. The limits of detection for the minute sample amounts are in the low picogram range. Graphical abstract.
微量元素对生命至关重要,其在细胞和组织中的浓度必须严格维持和控制,以避免病理状况。用于测量生物基质中微量元素浓度的既定方法通常只能提供单一元素信息,耗时且需要特殊的样品制备。因此,开发简单、快速的分析方法以增强生物样品中多痕量元素的测定是痕量元素分析的一个重要且不断发展的领域。在此,我们报告了一种基于全反射 X 射线荧光(TXRF)分析的可靠方法的开发和验证,该方法可精确地定量测定各种生物样品中的铁和其他痕量金属,例如肝脏、实质和非实质肝细胞以及骨髓衍生的巨噬细胞。我们表明,TXRF 允许通过添加内标进行快速而简单的单点校准,并且具有在微小样品量中进行多元素分析的潜力。该方法通过在 1 至 1600μg/L 的广泛浓度范围内用经过充分验证的石墨炉原子吸收光谱法(GFAAS)作为参考方法对匀浆中的铁进行回收实验进行了验证。99.93±0.14%的回收率表明不存在系统误差。此外,为了进一步验证生物金属的方法,还研究了标准参考物质“牛肝”(SRM 1577c,NIST)。铜、铁、锌和锰的定量回收率(92-106%)证明了所开发方法的适用性。对于微小的样品量,检测限在低皮克范围内。