Department of Chemistry, University of Pavia, 27100 Pavia, Italy.
Department of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Int J Environ Res Public Health. 2020 Jul 3;17(13):4782. doi: 10.3390/ijerph17134782.
The purpose of this study was to set up a sensitive method for the simultaneous determination of phycotoxins and cyanotoxins-Emerging pollutants with different structures and harmful properties (hepatotoxicity, neurotoxicity and cytotoxicity)-In environmental waters. Due to the low concentrations detected in these samples, a pre-concentration step is required and here it was performed in a single step with a commercial cartridge (Strata™-X), achieving enrichment factors up to 200 and satisfactory recovery (R = 70-118%) in different aqueous matrices. After solid-phase extraction (SPE), toxins were separated and quantified by High Performance Liquid Chromatography- Heated ElectroSpray Ionisation Tandem Mass Spectrometry (HPLC-HESI-MS/MS) in Multiple Reaction Monitoring (MRM) mode. An analytical evaluation of the proposed method was done based on the analytical figures of merit, such as precision and trueness, linearity, selectivity, and sensitivity, and it turned out to be a robust tool for the quantification of ng L levels, phycotoxins and cyanotoxins in both freshwater and saltwater samples.
本研究旨在建立一种灵敏的方法,用于同时测定环境水中具有不同结构和有害特性(肝毒性、神经毒性和细胞毒性)的新兴污染物——藻毒素和蓝藻毒素。由于这些样品中检测到的浓度较低,因此需要进行预浓缩步骤,这里采用商用柱(Strata™-X)一步完成,在不同的水基质中达到高达 200 的富集因子和令人满意的回收率(R = 70-118%)。固相萃取(SPE)后,毒素通过高效液相色谱-加热电喷雾串联质谱法(HPLC-HESI-MS/MS)在多重反应监测(MRM)模式下进行分离和定量。基于分析质量参数(如精密度和准确度、线性、选择性和灵敏度)对所提出的方法进行了分析评估,结果表明该方法是一种用于定量测定淡水和咸水样品中ng L 水平的藻毒素和蓝藻毒素的可靠工具。