[复合纯化柱-超高效液相色谱-串联质谱法同时测定鱼虾蟹中50种兽药残留]。

Hui-Dan Deng, Xiao-Feng Ji, Ying-Ping Xiao, Qiang Xia, Hua Yang
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引用次数: 0

摘要

中国是世界上最大的水产品生产国和消费国。杀虫剂以及兽药,如喹诺酮类药物、大环内酯类药物、硝基咪唑类药物、磺胺类药物和苯胺类药物,广泛用于水产养殖。这些化合物在预防、控制和治疗水生生物疾病、提高饲料转化率和促进养殖物种健康生长方面发挥着至关重要的作用。然而,养殖户非法使用兽药、过度使用兽药以及不遵守停药期限,都可能导致水产品含有兽药残留。本研究以鱼虾蟹为研究对象,旨在满足中国水产养殖业的绿色发展需求,加强风险预警和防范水产品兽药残留,提高养殖水产品的质量和竞争力,促进水产养殖业的可持续发展。优化仪器工作条件,确定提取溶剂、提取方法、纯化材料和样品前处理中使用的再溶溶剂。通过这些努力,建立了一套检测鱼、虾、蟹中喹诺酮类、大环内酯类、硝基咪唑类、磺胺类、霉素类和杀虫剂等50种兽药残留的方案,该方案采用复合纯化柱一步预处理结合超高效液相色谱-串联质谱(UPLC-MS/MS)。取5 g样品,用1.0%醋酸溶液提取,用无水硫酸钠脱水,用FAVEX纯化柱纯化,纯化后的溶液吹氮至近干。用0.2%甲酸-甲醇水溶液(9∶1,v/v)复溶1.0 mL,过滤后用Waters ACQUITY UPLC®BEH C18色谱柱(100 mm × 2.1 mm, 1.7 μm)分离。数据采集采用正离子和负离子多重反应监测模式,并采用同位素内外标进行量化。各目标化合物在各自的浓度范围内呈良好的线性关系,决定系数(R²)均大于0.990 0。鱼基质中50种兽药的平均回收率为60.1% ~ 117.8%,rsd为1.89% ~ 15.0%;虾基质的平均回收率为60.2% ~ 119.7%,rsd为1.11% ~ 15.6%;蟹基质的平均回收率为60.7% ~ 119.7%,rsd为2.94% ~ 15.0%。该方法具有预处理步骤简单、通量高、有机溶剂用量少、准确度好、灵敏度高、成本效益高等优点。采用建立的检测方法对150批水产品(包括50批鱼、50批虾、50批蟹)进行了50种兽药残留风险筛查。兽药残留检出率为47.3%,超标率为7.3%。其中,鱼类样品的检出率为66.0%,污染浓度为1.20 ~ 257.1 μg/kg。相比之下,虾类样品的检出率为18.0%,污染浓度为1.10 ~ 8.60 μg/kg,螃蟹样品的检出率分别为22.0%和3.00 ~ 7.30 μg/kg。本研究共检出佩氟沙星、诺氟沙星、环丙沙星、恩诺沙星、萨拉沙星、磺胺二甲氧嘧啶、磺胺甲恶唑7种兽药残留,检出率分别为0.67%、5.3%、12.7%、20.7%、4.6%、2.00%、1.33%。本研究建立的检测方法为及时监测和评估水产品风险提供了强有力的技术支持,有望在保障食品安全、保护消费者健康、促进水产品产业健康发展等方面发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Simultaneous determination of 50 veterinary drug residues in fish, shrimp, and crabs using a composite purification column-ultra-performance liquid chromatography-tandem mass spectrometry].

[Simultaneous determination of 50 veterinary drug residues in fish, shrimp, and crabs using a composite purification column-ultra-performance liquid chromatography-tandem mass spectrometry].

[Simultaneous determination of 50 veterinary drug residues in fish, shrimp, and crabs using a composite purification column-ultra-performance liquid chromatography-tandem mass spectrometry].

[Simultaneous determination of 50 veterinary drug residues in fish, shrimp, and crabs using a composite purification column-ultra-performance liquid chromatography-tandem mass spectrometry].

China is the world's largest producer and consumer of aquatic products. Insecticides, as well as veterinary drugs, such as quinolones, macrolides, nitroimidazoles, sulfonamides, and amphenicols, are widely used in aquaculture. These compounds play crucial roles in preventing, controlling, and treating diseases in aquatic organisms, improving feed conversion rates, and promoting the healthy growth of farmed species. However, the illegal use of veterinary drugs, their overuse, and noncompliance with drug withdrawal periods by farmers can lead to aquatic products containing veterinary drug residues. This study focused on fish, shrimp, and crabs with the aim of meeting the green-development needs of China's aquaculture industry, strengthening risk warnings and preventing veterinary drug residues in aquatic products, enhancing the quality and competitiveness of farmed aquatic products, and promoting the sustainable development of the aquaculture industry. Instrumental working conditions were optimized, and the extraction solvent, extraction method, purification materials, and the redissolution solvent used in the sample-pretreatment process were determined. These efforts led to the establishment of a protocol for the detection of 50 veterinary drug residues, including quinolones, macrolides, nitroimidazoles, sulfonamides, amphenicols, and insecticides, in fish, shrimp, and crabs, which involved one-step pretreatment with a composite purification column in combination with ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). A 5-g sample was extracted with a 1.0% acetic acid solution, dehydrated with anhydrous sodium sulfate, and purified using a FAVEX purification column, after which the purified solution was nitrogen-blown to near dryness. The residue was re-dissolved in 1.0 mL of 0.2% formic acid aqueous solution-methanol (9∶1, v/v) , filtered, and then separated using a Waters ACQUITY UPLC® BEH C18 column (100 mm × 2.1 mm, 1.7 μm). Data were collected in positive- and negative-ion multiple reaction monitoring modes, and quantified using isotopic internal and external standards. All target compounds exhibited good linear relationships within their respective concentration ranges, with coefficients of determination (R²) greater than 0.990 0. Average recovery rates of 60.1%-117.8% were determined for the 50 veterinary drugs in the fish matrix, with RSDs of between 1.89% and 15.0%, while the shrimp matrix delivered average recovery rates of 60.2%-119.7%, with RSDs of 1.11%-15.6%, and the crab matrix exhibited average values of 60.7%-119.7% and 2.94%-15.0%, respectively. The developed method is advantageous owing to its simple pretreatment step, high throughput, low organic-solvent consumption, good accuracy, high sensitivity, and cost-effectiveness. One hundred and fifty batches of aquatic products, including 50 batches of fish, 50 batches of shrimp, and 50 batches of crab, were risk-screened for 50 veterinary drug residues using the established detection method. Veterinary drug residues were detected at a rate of 47.3%, with an over-standard rate of 7.3%. Specifically, the fish samples exhibited a detection rate of 66.0%, with contamination concentrations of 1.20-257.1 μg/kg. In contrast, the shrimp samples exhibited a detection rate of 18.0%, with contamination concentrations of 1.10-8.60 μg/kg, while values of 22.0% and 3.00-7.30 μg/kg, respectively, were determined for the crab samples. This study identified a total of seven veterinary drug residues, namely pefloxacin, norfloxacin, ciprofloxacin, enrofloxacin, sarafloxacin, sulfadimethoxine, and sulfamethoxazole, with detection rates of 0.67%, 5.3%, 12.7%, 20.7%, 4.6%, 2.00%, and 1.33%, respectively. The detection method established in this study provides strong technical support for monitoring and assessing aquatic-product risks in a timely manner, and is expected play an important role in ensuring food safety, protecting consumer health, and promoting the healthy development of the aquatic-product industry.

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