Mu Yinghua, Xing Jiali, Shen Jian, Ying Lu, Mao Lingyan, Xu Xiaorong, Lou Yongjiang, Wu Xi
College of Food and Pharmaceutical Sciences, Ningbo University, Ningbo 315211, China; Ningbo Academy of Product and Food Quality Inspection (Ningbo Fibre Inspection Institute), Ningbo 315048, China.
Ningbo Academy of Product and Food Quality Inspection (Ningbo Fibre Inspection Institute), Ningbo 315048, China.
Se Pu. 2022 May 8;40(5):477-487. doi: 10.3724/SP.J.1123.2021.12002.
With the increasing use of chlorine-containing pesticides, hypochlorous acid disinfection water as well as aquatic product insecticides and fungicides are widely used in the cultivation of fish. This has led to the contamination of fish by chlorophenol compounds. However, currently, there is no standard method for the simultaneous determination of 19 chlorophenol compounds in fish. In this study, the optimum chromatography and mass spectrometry conditions were determined by investigating the instrument parameters. The 19 chlorophenol compounds were well separated using the DB-5MS capillary chromatographic column (30 m×0.25 mm×0.25 μm) with a carrier gas flow rate of 1 mL/min. Under this condition, the chromatographic peak was sharp and symmetric. An analytical method was developed for the simultaneous determination of the 19 chlorophenol compounds in fish using gas chromatography-mass spectrometry coupled with QuEChERS pretreatment. The improved QuEChERS method was used in sample preparation. The 19 chlorophenol compounds were extracted with organic solvents and purified with purifying agents. During the experiment, the effect of the kinds and volumes of the extraction solvent, as well as the types and dosages of the purifying agent, on the recoveries of the 19 chlorophenol compounds were investigated. Moreover, the temperature and time of derivatization, as well as the dosage of the derivatization agent, were optimized. All aforementioned analyses were conducted with the aim of determining the optimal pretreatment method. Finally, the optimized gas chromatography-mass spectrometry conditions were employed for the quantitative determination of 19 chlorophenol compounds in fish samples. Based on the experimental results, the best extraction method was determined to be the one where the extraction agent (10 mL ethyl acetate) was added to 3 g sodium chloride and 5 g anhydrous magnesium sulfate in the test tube, followed by ultrasonication for 15 min. The sample was centrifuged at 4500 r/min for 5 min, and 500 mg C was selected as the purifying agent to purify the supernatant. The purified supernatant was blown with nitrogen to less than 1 mL at 45 ℃, and then redissolved with ethyl acetate to 1 mL. Subsequently, the sample solution was passed through a 0.22 μm organic filter membrane, following which 50 μL bis(trimethylsilyl)trifluoroacetamide was added for derivatization at 45 ℃ for 30 min. Lastly, the 19 chlorophenol compounds were determined by gas chromatography-mass spectrometry with an electrospray ionization source and selecting ion monitoring mode. The 19 chlorophenol compounds were then quantitatively analyzed by the external standard method. The compounds showed good linearity in the concentration range of 0.4-10 μg/L, with correlation coefficients () greater than 0.998. The limits of detection and limits of quantification were 0.01-0.05 μg/kg and 0.04-0.16 μg/kg, respectively. Moreover, the average recoveries of the 19 chlorophenol compounds were in the range of 70.6%-115.0% at three spiked levels, and the relative standard deviations were in the range of 2.6%-10.5%. The established method in this study was applied to detect and analyze chlorophenol compounds in actual samples. The experimental results showed that various levels of chlorophenol compounds could be detected in different fishes. Among them, the total amount of chlorophenol compounds detected in the Corvina was 8.74 μg/kg, followed by the Crucian carp at 7.59 μg/kg, and the minimum detected amount in rice fish (1.59 μg/kg). With its simple operation, high sensitivity, and good repeatability, the established method simplifies the pre-treatment of fish samples. It can also meet the requirements for the high-throughput detection of 19 chlorophenol compounds in fish, thereby significantly improving the detection efficiency of chlorophenols. Moreover, the method provides crucial technical support and a theoretical basis for the establishment of feasible detection standards for chlorophenols in China, as well as for the control of residue levels of chlorophenol compounds in fish. The findings have important practical significance to implement management measures during fish breeding and transportation.
随着含氯农药使用的增加,次氯酸消毒水以及水产品杀虫剂和杀菌剂在鱼类养殖中被广泛使用。这导致了氯酚化合物对鱼类的污染。然而,目前尚无同时测定鱼类中19种氯酚化合物的标准方法。本研究通过考察仪器参数确定了最佳的色谱和质谱条件。采用DB-5MS毛细管色谱柱(30 m×0.25 mm×0.25μm),载气流速为1 mL/min,19种氯酚化合物得到了良好的分离。在此条件下,色谱峰尖锐且对称。建立了气相色谱-质谱联用结合QuEChERS预处理同时测定鱼类中19种氯酚化合物的分析方法。改进的QuEChERS方法用于样品制备。用有机溶剂萃取19种氯酚化合物,并用净化剂进行净化。实验过程中,考察了萃取溶剂的种类和体积以及净化剂的类型和用量对19种氯酚化合物回收率的影响。此外,对衍生化温度、时间以及衍生化试剂用量进行了优化。所有上述分析旨在确定最佳的预处理方法。最后,采用优化的气相色谱-质谱条件对鱼类样品中的19种氯酚化合物进行定量测定。根据实验结果,确定最佳萃取方法为:在试管中加入3 g氯化钠、5 g无水硫酸镁和10 mL乙酸乙酯萃取剂,超声15 min。样品在4500 r/min下离心5 min,选用500 mg C作为净化剂净化上清液。净化后的上清液在45℃下用氮气吹至小于1 mL,然后用乙酸乙酯重新溶解至1 mL。随后,样品溶液通过0.22μm有机滤膜,接着加入50μL双(三甲基硅基)三氟乙酰胺在45℃下衍生化30 min。最后,采用电喷雾电离源和选择离子监测模式的气相色谱-质谱法测定19种氯酚化合物。然后用外标法对19种氯酚化合物进行定量分析。这些化合物在0.4 - 10μg/L浓度范围内线性良好,相关系数()大于0.998。检测限和定量限分别为0.01 - 0.05μg/kg和0.04 - 0.16μg/kg。此外,19种氯酚化合物在三个加标水平下的平均回收率在70.6% - 115.0%范围内,相对标准偏差在2.6% - 10.5%范围内。本研究建立的方法应用于实际样品中氯酚化合物的检测分析。实验结果表明,不同鱼类中均可检测到不同含量的氯酚化合物。其中,检测到的军曹鱼中氯酚化合物总量为8.74μg/kg,其次是鲫鱼,为7.59μg/kg,而泥鳅中检测到的含量最低(1.59μg/kg)。所建立的方法操作简单、灵敏度高、重复性好,简化了鱼类样品的预处理。它还能满足鱼类中19种氯酚化合物高通量检测的要求,从而显著提高氯酚的检测效率。此外,该方法为我国建立可行的氯酚检测标准以及控制鱼类中氯酚化合物残留水平提供了关键的技术支持和理论依据。研究结果对实施鱼类养殖和运输过程中的管理措施具有重要的实际意义。