Optimization of a rapid QuEChERS sample treatment method for HILIC-MS2 analysis of paralytic shellfish poisoning (PSP) toxins in mussels

被引:23
作者
Mattarozzi, Monica [1 ]
Milioli, Marco [1 ]
Bianchi, Federica [1 ]
Cavazza, Antonella [1 ]
Pigozzi, Silvia [2 ]
Milandri, Anna [2 ]
Careri, Maria [1 ]
机构
[1] Univ Parma, Dipartimento Chim, I-43124 Parma, Italy
[2] Fdn Ctr Ric Marine, Lab Nazl Riferimento Biotossine Marine, I-47042 Cesenatico, FC, Italy
关键词
Paralytic shellfish poisoning (PSP) toxins; Hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS2); Mussels; QuEChERS; Experimental design optimization; HIGH-THROUGHPUT ANALYSIS; CHROMATOGRAPHY-MASS SPECTROMETRY; SOLID-PHASE EXTRACTION; LIQUID-CHROMATOGRAPHY; GAS-CHROMATOGRAPHY; QUANTIFICATION; PESTICIDES; SAXITOXIN; PRODUCTS; FRESH;
D O I
10.1016/j.foodcont.2015.07.027
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A rapid and simple QuEChERS sample treatment was proposed for the development of a selective hydrophilic interaction liquid chromatography-ESI-MS2-based method for the determination of saxitoxins (STXs) in mussel samples. Among different sorbents, ABS Elut-NEXUS phase, composed of polystyrene cross-linked with 50% divinyl benzene and poly(methyl methacrylate), provided the best results. The effects of experimental parameters, including sorbent amount, vortexing time and centrifugation time were investigated and optimized by experimental design. In particular, regression models and desirability functions were applied to find the experimental conditions providing the highest global extraction response. The method was validated under the optimized conditions; detection and quantification limits in the 3-159 mu g/kg and 7-436 mu g/kg ranges respectively were obtained, except for C2 for which highest values were calculated due to its low ESI ionization efficiency. Finally, the analysis of twenty-eight mussel samples permitted to detect and quantify some of the investigated SDCs, proving the applicability of the devised method. (c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
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