Environmental Engineering Department, Federal University of Paraná, Curitiba, Brazil.
Ecology and Environment Research Centre, Department of Natural Sciences, Manchester Metropolitan University, Manchester, UK.
Appl Spectrosc. 2020 Aug;74(8):932-939. doi: 10.1177/0003702820906422.
Recent studies to quantify the health risks that fine particulate matter with an aerodynamic less than 2.5 µm (PM) pose use in vitro approaches. One of these approaches is to incubate PM in artificial lysosomal fluid for a given period at body temperature. These body fluids used have a high ionic strength and as such can be challenging samples to analyze with atomic spectroscopy techniques. As PM is a primary health hazard because it is tiny enough to penetrate deep into the lungs and could, in addition, dissolve in the lung fluid it is important to quantify elements of toxic and/or carcinogenic concerns, reliably and accurately. Sophisticated instrumentation and expensive pre-treatment of challenging samples are not always available, especially in developing countries. To evaluate the applicability of graphite furnace atomic absorption spectrometry (GFAAS) without Zeeman correction capability to detect trace quantities of heavy metals leached from PM on to artificial lung fluid, univariate and multivariate approaches have been used for optimization purposes. The limits of quantification, LOQ, obtained by the optimized method were: 2 µg L (Cu), 3 µg L (Cr), 1 µg L (Mn), and 10 µg L (Pb). The addition/recovery experiments had a mean accuracy of: (Cu) 99 ± 7%; 110 ± 8% (Cr); 95 ± 9% (Mn), and 96 ± 11% (Pb). The average soluble fractions of PM incubated in artificial lysosomal fluid (ALF) for 1 h were: 1.2 ± 0.01 ng m Cu, 0.4 ± 0.01 ng m Cr, 0.6 ± 0.01 ng m Mn, and 4.8 ± 0.03 ng m Pb. Using historical elemental averages of PM in Curitiba (Cu 3.3 ng m, Cr 2.1 ng m, Mn 6.1 ng m, Pb 21 ng m), the percentage bioaccessibility were determined to be Cu 38%, Cr 20%, Mn 10%, and Pb 23%. The elemental values of the atmospheric soluble fraction of Cu, Cr, and Mn were below the inhalation risk concentrations. However, for Pb, the atmospheric soluble fraction exceeded the inhalation unit risk of 0.012 ng m. This robust and straightforward GF AAS method is pivotal for low and middle-income countries were most air pollution adverse effects occur and established lower-cost technologies are likely unavailable.
最近的研究使用体外方法来量化小于 2.5μm 的空气动力学直径的细颗粒物(PM)所带来的健康风险。这些方法之一是将 PM 在人工溶酶体液中在体温下孵育一段时间。这些体液具有很高的离子强度,因此对于原子光谱技术分析来说是具有挑战性的样本。由于 PM 是一种主要的健康危害,因为它足够小,可以穿透到肺部深处,并且可能会溶解在肺部液体中,因此准确可靠地量化其毒性和/或致癌性元素非常重要。复杂的仪器设备和具有挑战性的样本的昂贵预处理并非总是可用,尤其是在发展中国家。为了评估无塞曼校正功能的石墨炉原子吸收光谱法(GFAAS)在检测溶解于人工肺液中的 PM 中痕量重金属方面的适用性,已经使用了单变量和多变量方法来进行优化。通过优化方法获得的定量下限(LOQ)为:2μg L(Cu),3μg L(Cr),1μg L(Mn)和 10μg L(Pb)。加标/回收实验的平均准确度为:(Cu)99±7%;110±8%(Cr);95±9%(Mn)和 96±11%(Pb)。在人工溶酶体液(ALF)中孵育 1 小时的 PM 的平均可溶性分数为:1.2±0.01ng m Cu,0.4±0.01ng m Cr,0.6±0.01ng m Mn 和 4.8±0.03ng m Pb。使用库里蒂巴(Cu 3.3ng m,Cr 2.1ng m,Mn 6.1ng m,Pb 21ng m)的 PM 元素平均值,确定 Cu 的生物可利用百分比为 38%,Cr 为 20%,Mn 为 10%,Pb 为 23%。Cu、Cr 和 Mn 的大气可溶性部分的元素值低于吸入风险浓度。然而,对于 Pb,大气可溶性部分超过了 0.012ng m 的吸入单位风险。这种稳健而简单的 GF AAS 方法对于大多数空气污染不良影响发生的中低收入国家至关重要,因为那里可能无法获得更具成本效益的技术。