SAMRC, Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa.
Department of Pure and Applied Chemistry, University of Fort Hare, Alice 5700, South Africa.
Molecules. 2020 Jul 8;25(14):3114. doi: 10.3390/molecules25143114.
The validation of a sensitive and reliable analytical procedure for the determination of pharmaceutical and personal care products (PPCPs) in solid environmental samples is reported in this study. Initially, two types of derivatization were used for the identification of the 13 target PPCP standards (acylation and silylation), but silylation proved to be better in sensitivity as it detected all of the analytes under investigation. Samples were extracted using an ultrasonicator, concentrated and re-dissolved in 100 mL water, then cleaned-up using C18 cartridges before silylation that preceded the Gas chromatography-mass Spectrometry detector (GC-MS) analyses. The optimized method provided a linear response over the range of 10-400 ng·g with r > 0.992 and satisfactory recoveries (>45.6%) for the 13 compounds of interest. In this study, the variation of the sonication temperature, type of organic solvent for extraction, and types of cartridge were used to optimize the extraction procedure. A good repeatability (within day) and reproducibility (between days) with a relative standard deviation (RSD) that was equal or less than 13% for all the PPCPs were achieved with the developed extraction procedures for the irrigated soil and sewage sludge samples. The limits of detection (LODs) of the tested compounds varied from 0.1 ng·g (aspirin) to 1.4 ng·g (doxycycline) and from 0.1 ng·g (codiene) to 1.7 ng·g (doxycycline) for soils and sewage sludge samples, respectively. The method was successfully applied to the sludge of wastewater treatment plants and soils of an irrigated golf course. Among the tested emerging pollutants, paracetamol showed the highest concentration value of 98.9 ng·g in the sludge, and for the irrigated soil (0 to 10 cm), the concentration ranged from 1.16 ng·g (aspirin) to 8.57 ng·g (ibuprofen).
本研究报告了一种用于测定环境固体样品中药物和个人护理产品(PPCP)的灵敏、可靠的分析方法的验证。最初,使用两种衍生化方法(酰化和硅烷化)来鉴定 13 种目标 PPCP 标准品,但硅烷化在灵敏度方面表现更好,因为它可以检测到所有被研究的分析物。样品使用超声提取器提取,浓缩后重新溶解在 100 mL 水中,然后使用 C18 小柱进行净化,再进行硅烷化,最后进行气相色谱-质谱联用(GC-MS)分析。优化后的方法在 10-400 ng·g 范围内呈现线性响应,相关系数(r)大于 0.992,对于 13 种感兴趣的化合物,回收率均大于 45.6%。在本研究中,使用超声温度、提取用有机溶剂类型和小柱类型的变化来优化提取程序。对于灌溉土壤和污水污泥样品,开发的提取程序具有良好的日内和日间重复性,相对标准偏差(RSD)等于或小于 13%。所有测试化合物的检出限(LOD)从 0.1 ng·g(阿司匹林)到 1.4 ng·g(强力霉素)不等,从 0.1 ng·g(可待因)到 1.7 ng·g(强力霉素)不等,分别用于土壤和污水污泥样品。该方法成功应用于污水处理厂的污泥和灌溉高尔夫球场的土壤。在所测试的新兴污染物中,对乙酰氨基酚在污泥中的浓度最高,为 98.9 ng·g,而在灌溉土壤(0 至 10 cm)中,浓度范围为 1.16 ng·g(阿司匹林)至 8.57 ng·g(布洛芬)。