Calbiani F, Careri M, Elviri L, Mangia A, Zagnoni I
Dipartimento di Chimica Generale ed Inorganica, Chimica Analitica, Chimica Fisica, Università degli Studi di Parma, 43100 Parma, Italy.
Food Addit Contam. 2007 Aug;24(8):833-41. doi: 10.1080/02652030701278339.
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.
报道了一种基于离子对液相色谱 - 电喷雾串联质谱(LC - MS/MS)的方法,用于测定肉类婴儿食品中的杂环芳香胺(HAA)。这些杂环芳香胺包括喹啉(IQ、MeIQ)、喹喔啉(MeIQx)、吡啶(PhIP)和咔啉衍生物(AαC、哈尔满、去甲哈尔满),以d(3)-IQ、(13)C(2)-MeIQx和d(3)-PhIP作为标记内标。该方法先用丙酮萃取,然后在SCX固相萃取柱上进行净化。液相色谱分离在TSKgel ODS - 80TS柱(250×2.0 mm,5μm)上进行,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)。为明确鉴定每种分析物,检测三个离子并选择用于选择反应监测(SRM)。在冻干肉类样品上进行了方法验证。不同分析物的平均回收率在78±4%至98±2%之间。在所研究的肉类样品中,所研究分析物的定量限通常低于8 ng g(-1)。该方法具有良好的线性和重复性。稳健性测试确定了在影响色谱分离和响应方面具有统计学意义的因素,并指出了为可靠分析杂环芳香胺必须严格控制的参数。特别是,发现流动相流速对于除AαC峰外所有分析物的容量因子(k')具有统计学意义(α = 0.05),而流动相pH值是IQ、MeIQ和去甲哈尔满k'值的关键参数。该方法在IQ和MeIQ峰之间的分离度方面被证明具有稳健性。在质谱参数中,发现碰撞能量除了对IQ外,对所有分析物的定量响应有显著影响。证明了该方法在肉类婴儿食品样品分析中的适用性。