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高通量 UHPLC-MS/MS 法测定欧盟法规脂溶性海洋贝类毒素的优化与验证及贝类鲜品和制品中的分布

Optimization and Validation of a High Throughput UHPLC-MS/MS Method for Determination of the EU Regulated Lipophilic Marine Toxins and Occurrence in Fresh and Processed Shellfish.

机构信息

Istituto Zooprofilattico Sperimentale della Puglia e della Basilicata, Via Manfredonia 20, 71121 Foggia, Italy.

出版信息

Mar Drugs. 2022 Feb 26;20(3):173. doi: 10.3390/md20030173.

Abstract

Under the name of lipophilic marine toxins, there are included more than 1000 toxic secondary metabolites, produced by phytoplankton, with the common chemical property of lipophilicity. Due to toxicological effects and geographical distribution, in European legislation relevant compounds are regulated, and their determination is accomplished with the reference liquid chromatography-tandem mass spectrometry method. In this study a modified ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method has been developed for the identification and quantification of EU-regulated lipophilic toxins. The method optimization included a refinement of SPE-C18 clean-up, in order to reduce matrix interferences. Improved LC conditions and upgraded chromatographic ammonia-based gradient ensured the best separation of all analytes and, in particular, of the two structural isomers (OA and DTX2). Also, different MS parameters were tested, and confirmation criteria finally established. The validation studies confirmed that all parameters were satisfactory. The requirements for precision (RSD% < 11.8% for each compound), trueness (recoveries from 73 to 101%) and sensitivity (limits of quantification in the range 3−8 µg kg−1) were fulfilled. The matrix effect, ranging from −9 to 19%, allowed the use of a calibration curve in solvent (3−320 µg kg−1 in matrix) for quantification of real samples. Method relative uncertainty ranged from 12 to 20.3%. Additionally, a total of 1000 shellfish samples was analysed, providing a first preliminary surveillance study that may contribute to the knowledge of lipophilic marine toxins contamination. Increase in algae proliferation events and intoxication cases, EFSA suggestions for modification of maximum permitted levels and toxicity equivalency factors, and new studies of important toxic effects underline that implementation of reference methods still represents an important task for health and food safety laboratories.

摘要

在亲脂性海洋毒素的名称下,有超过 1000 种有毒的次生代谢物,这些代谢物由浮游植物产生,具有亲脂性的共同化学性质。由于毒性作用和地理分布,欧洲法规对相关化合物进行了监管,其测定采用参考液相色谱-串联质谱法。在这项研究中,开发了一种改良的超高效液相色谱-串联质谱法(UHPLC-MS/MS),用于鉴定和定量欧盟监管的亲脂性毒素。方法优化包括 SPE-C18 净化的改进,以减少基质干扰。改进的 LC 条件和升级的基于氨的色谱梯度确保了所有分析物的最佳分离,特别是两种结构异构体(OA 和 DTX2)的分离。此外,还测试了不同的 MS 参数,并最终确定了确认标准。验证研究证实所有参数均令人满意。对精密度(每个化合物的 RSD%<11.8%)、准确度(回收率为 73%至 101%)和灵敏度(定量限在 3-8μg kg-1范围内)的要求均得到满足。基质效应在-9%至 19%之间,允许使用溶剂中的校准曲线(基质中 3-320μg kg-1)对实际样品进行定量。方法相对不确定度范围为 12%至 20.3%。此外,总共分析了 1000 个贝类样本,进行了首次初步监测研究,这可能有助于了解亲脂性海洋毒素的污染情况。藻类增殖事件和中毒病例的增加、EFSA 对最大允许水平和毒性等效因子进行修改的建议,以及对重要毒性作用的新研究表明,实施参考方法仍然是健康和食品安全实验室的一项重要任务。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f766/8953077/b3b436342b68/marinedrugs-20-00173-g001.jpg

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