离子对液相色谱-电喷雾-串联质谱法测定婴儿肉类食品中杂环芳香胺的验证。

F Calbiani, M Careri, L Elviri, A Mangia, I Zagnoni
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引用次数: 13

摘要

报道了一种基于离子对液相色谱-电喷雾串联质谱(LC-MS/MS)的测定肉类婴儿食品中杂环芳香胺(HAAs)的方法。HAAs包括喹啉(IQ, MeIQ),喹啉(MeIQx),吡啶(PhIP)和羰基衍生物(AalphaC, Harman, Norharman),其中d(3)-IQ, (13)C(2)-MeIQx和d(3)-PhIP作为标记内标。该方法采用提取丙酮,然后在SCX固相萃取柱上进行清理。色谱柱为TSKgel ODS-80TS (250 × 2.0 mm, 5微米),流动相为甲酸铵-甲酸缓冲液(3.03 mm甲酸铵,pH = 2.8)水溶液-乙腈梯度,流速为0.2 ml min(-1)。为了明确鉴定每种分析物,检测三个离子并选择用于选定的反应监测(SRM)。对冻干肉类样品进行了验证。不同分析物的平均回收率在78 +/- 4%和98 +/- 2%之间。定量限通常低于8 ng g(-1)在肉类样品中被证实为所调查的分析物。该方法具有良好的线性和重复性。鲁棒性检验确定了影响色谱分离和响应的有统计学意义的因素,并指出哪些参数必须严格控制才能可靠地分析HAAs。特别是,除AalphaC峰外,所有分析物的容量因子(k′)的流动相流速均具有统计学意义(α = 0.05),而流动相pH是IQ、MeIQ和Norharman的k′值的关键参数。结果表明,该方法具有较好的鲁棒性。在质谱参数中,除IQ外,碰撞能量对分析物的定量响应均有显著影响。验证了该方法对婴儿肉类食品样品分析的适用性。
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Validation of an ion-pair liquid chromatography-electrospray-tandem mass spectrometry method for the determination of heterocyclic aromatic amines in meat-based infant foods.

A method based on ion-pair liquid chromatography-electrospray tandem mass spectrometry (LC-MS/MS) is reported for determining heterocyclic aromatic amines (HAAs) in meat-based infant foods. The HAAs encompassed quinoline (IQ, MeIQ), quinoxaline (MeIQx), pyridine (PhIP), and carboline derivatives (AalphaC, Harman, Norharman) with d(3)-IQ, (13)C(2)-MeIQx, and d(3)-PhIP used as labelled internal standards. The method used extraction into acetone followed by a clean-up on an SCX solid-phase extraction column. LC separation was performed on a TSKgel ODS-80TS column (250 x 2.0 mm, 5 microm), the mobile phase being an ammonium formate-formic acid buffer (3.03 mM ammonium formate, pH = 2.8) aqueous solution-acetonitrile gradient at a flow rate of 0.2 ml min(-1). For unequivocal identification of each analyte, three ions were detected and chosen for selected reaction monitoring (SRM). Validation was carried out on lyophilized meat samples. Mean recoveries ranged between 78 +/- 4% and 98 +/- 2% for different analytes. Limits of quantification generally lower than 8 ng g(-1) were demonstrated in meat samples for the analytes investigated. The method exhibited a good linearity and repeatability. Robustness testing identified those factors which were statistically significant in influencing chromatographic separation and response, and indicated which parameters have to be strictly controlled for a reliable analysis of HAAs. In particular, the mobile-phase flow rate was found to be statistically significant (alpha = 0.05) for the capacity factor (k') of all analytes except for AalphaC peak, whereas the mobile-phase pH resulted to be a critical parameter for the k' values of IQ, MeIQ, and Norharman. The method was proved to be robust vs. resolution between IQ and MeIQ peaks. Among mass-spectrometric parameters, collision energy was found to significantly affect quantitative response of all analytes except that of IQ. The applicability of the method to the analysis of meat-based infant food samples was demonstrated.

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