Orellana Gabriel, Vanden Bussche Julie, Van Meulebroek Lieven, Vandegehuchte Michiel, Janssen Colin, Vanhaecke Lynn
Faculty of Veterinary Medicine, Department of Veterinary Public Health and Food Safety, Laboratory of Chemical Analysis, Ghent University, Salisburylaan 133, 9820, Merelbeke, Belgium.
Anal Bioanal Chem. 2014 Sep;406(22):5303-12. doi: 10.1007/s00216-014-7958-6. Epub 2014 Jun 18.
Lipophilic marine toxins are produced by harmful microalgae and can accumulate in edible filter feeders such as shellfish, leading to an introduction of toxins into the human food chain, causing different poisoning effects. During the last years, analytical methods, based on liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS), have been consolidated by interlaboratory validations. However, the main drawback of LC-MS/MS methods remains the limited number of compounds that can be analyzed in a single run. Due to the targeted nature of these methods, only known toxins, previously considered during method optimization, will be detected. Therefore in this study, a method based on ultra-high-performance liquid chromatography coupled to high-resolution Orbitrap mass spectrometry (UHPLC-HR-Orbitrap MS) was developed. Its quantitative performance was evaluated for confirmatory analysis of regulated lipophilic marine toxins in shellfish flesh according to Commission Decision 2002/657/EC. Okadaic acid (OA), dinophysistoxin-1 (DTX-1), pectenotoxin-2 (PTX-2), azaspiracid-1 (AZA-1), yessotoxin (YTX), and 13-desmethyl spirolide C (SPX-1) were quantified using matrix-matched calibration curves (MMS). For all compounds, the reproducibility ranged from 2.9 to 4.9 %, repeatability from 2.9 to 4.9 %, and recoveries from 82.9 to 113 % at the three different spiked levels. In addition, confirmatory identification of the compounds was effectively performed by the presence of a second diagnostic ion ((13)C). In conclusion, UHPLC-HR-Orbitrap MS permitted more accurate and faster detection of the target toxins than previously described LC-MS/MS methods. Furthermore, HRMS allows to retrospectively screen for many analogues and metabolites using its full-scan capabilities but also untargeted screening through the use of metabolomics software.
亲脂性海洋毒素由有害微藻产生,可在贝类等可食用滤食性动物体内蓄积,导致毒素进入人类食物链,引发不同的中毒效应。在过去几年中,基于液相色谱-串联质谱联用(LC-MS/MS)的分析方法已通过实验室间验证得到巩固。然而,LC-MS/MS方法的主要缺点仍然是单次运行中可分析的化合物数量有限。由于这些方法的靶向性质,只会检测到在方法优化过程中预先考虑的已知毒素。因此,在本研究中,开发了一种基于超高效液相色谱-高分辨率轨道阱质谱联用(UHPLC-HR-Orbitrap MS)的方法。根据欧盟委员会第2002/657/EC号决定,对其定量性能进行了评估,用于贝类肉中受监管的亲脂性海洋毒素的确证分析。使用基质匹配校准曲线(MMS)对冈田酸(OA)、鳍藻毒素-1(DTX-1)、pectenotoxin-2(PTX-2)、azaspiracid-1(AZA-1)、岩沙海葵毒素(YTX)和13-去甲基螺旋环内酯C(SPX-1)进行定量。对于所有化合物,在三种不同加标水平下,重现性范围为2.9%至4.9%,重复性范围为2.9%至4.9%,回收率范围为82.9%至113%。此外,通过第二个诊断离子((13)C)的存在有效地进行了化合物的确证鉴定。总之,与先前描述的LC-MS/MS方法相比,UHPLC-HR-Orbitrap MS能够更准确、更快地检测目标毒素。此外,高分辨率质谱(HRMS)不仅可以利用其全扫描功能对许多类似物和代谢物进行回顾性筛查,还可以通过使用代谢组学软件进行非靶向筛查。