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Detection of free microcystins in the liver and muscle of freshwater fish by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法检测淡水鱼肝和肌肉中的游离微囊藻毒素

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摘要

MC analysis of biological tissue is considered to be very difficult due to the lack of validated methods. This is the primary limiting factor for monitoring potential risks in both the flesh of aquatic organisms and the aquatic ecosystem. In this study, an effective method to determine free MCs (MC-LR and MC-RR) in the muscle and liver tissues of freshwater cultured fish was developed using solid-phase extraction (SPE) and liquid chromatography-tandem mass spectrometry (LC/MS-MS). The extraction solvent, time of extraction, eluent and purification of the extract were optimized. Various SPE cartridges were also investigated. In this optimized analytical procedure, an 85% methanol/water solution (v/v) was selected as the extraction solvent, after which the extracts were purified by removing fats and proteins; a HLB cartridge was chosen for MCs enrichment; and 90% methanol containing 0.02% formic acid/water solution (v/v) was used as the eluent. Under the optimized pretreatment conditions and instrument parameters, good recoveries of MC-LR and MC-RR were obtained at three concentrations (0.5, 1.0 and 2.0 μg g~(-1) dry weight (DW)), with values ranging from 92.5 to 98.3% and 92.1 to 98.6%, respectively. The method detection limit (MDL) for muscle samples was 0.5 μg kg~(-1) and 0.4 μg kg~(-1) (DW) for MC-LR and MC-RR, respectively. The MDL for the liver samples was 0.8 μg kg~(-1) (DW) for both MC-LR and MC-RR. The developed procedure was successfully applied to analyze MCs in the muscle and liver of fish samples collected from a Chinese freshwater aquaculture pond during bloom seasons. The MC-LR concentrations ranged from below the MDL to 4.17 μg kg~(-1) and the MC-RR concentrations ranged from below the MDL to 2.64 μg kg~(-1).
机译:由于缺乏经过验证的方法,生物组织的MC分析被认为非常困难。这是监测水生生物肉和水生生态系统中潜在风险的主要限制因素。在这项研究中,开发了一种使用固相萃取(SPE)和液相色谱-串联质谱(LC / MS)测定淡水养殖鱼的肌肉和肝脏组织中游离MC(MC-LR和MC-RR)的有效方法MS-MS)。优化了提取溶剂,提取时间,洗脱液和提取液的纯化。还研究了各种SPE滤芯。在此优化的分析程序中,选择了85%的甲醇/水溶液(v / v)作为萃取溶剂,然后通过去除脂肪和蛋白质来纯化萃取物。选择了HLB小柱进行MC富集;用含有0.02%甲酸/水溶液(v / v)的90%甲醇作为洗脱液。在优化的预处理条件和仪器参数下,三种浓度(0.5、1.0和2.0μgg〜(-1)干重(DW))的MC-LR和MC-RR均具有良好的回收率,其值范围为92.5至分别为98.3%和92.1至98.6%。肌肉样品的方法检出限(MDL)对于MC-LR和MC-RR分别为0.5μgkg〜(-1)和0.4μgkg〜(-1)(DW)。肝样本的MDL对于MC-LR和MC-RR均为0.8μgkg〜(-1)(DW)。所开发的程序已成功地用于分析盛开季节从中国淡水养殖池塘采集的鱼样品的肌肉和肝脏中的多氯联苯。 MC-LR的浓度范围从MDL以下至4.17μgkg〜(-1),MC-RR的浓度范围从MDL以下至2.64μgkg〜(-1)。

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