Domingo Elisângela do Carmo, Tireli Aline Auxiliadora, Nunes Cleiton Antonio, Batista Alexandre Vieira, Guerreiro Mário César, Pinto Sandra Maria
Department of Food Science, Federal University of Lavras, Lavras, Minas Gerais, Brazil.
Department of Chemistry, Federal University of Lavras, Lavras, Minas Gerais, Brazil.
Talanta. 2015 Jan;132:535-40. doi: 10.1016/j.talanta.2014.10.003. Epub 2014 Oct 22.
A combination of a simple pretreatment for melamine extraction and direct analysis in electrospray ionization tandem mass spectrometry (ESI-MS/MS) is proposed. Three pretreatments were evaluated. The first was based on suppressing interference using acetonitrile. The second used sulphuric acid and trichloroacetic acid to suppress interference and for melamine extraction, respectively. The third used sulphuric acid to suppress milk interference, trichloroacetic acid for melamine precipitation, and ethyl acetate for melamine extraction. However, only the last pretreatment suppressed milk interference in melamine detection and a good linearity (R(2)=0.99) was obtained. The presence of MS/MS 85 on melamine fragmentation spectrum showed the selectivity of this method. The limit of detection and limit of quantification were 0.269 µg L(-1) and 0.897 µg L(-1), respectively. The recoveries and relative standard deviation (RDS) of method were lower than 114% and 7.86%, respectively. Further, the research was extended to elucidate the nature of the melamine in the extract through infrared spectroscopy and microscopy analyses. The precipitate was characterized as melaminium bis(trichloroacetate) dihydrate, which is generated through hydrogen bound formation in an interaction between melamine and trichloroacetic acid. Therefore, a simple, fast, and easy method for melamine extraction and direct ESI-MS/MS analysis was developed.
本文提出了一种将三聚氰胺萃取的简单预处理方法与电喷雾电离串联质谱(ESI-MS/MS)直接分析相结合的方法。对三种预处理方法进行了评估。第一种方法是基于使用乙腈抑制干扰。第二种方法分别使用硫酸和三氯乙酸来抑制干扰和萃取三聚氰胺。第三种方法使用硫酸抑制牛奶干扰,用三氯乙酸使三聚氰胺沉淀,并用乙酸乙酯萃取三聚氰胺。然而,只有最后一种预处理方法在三聚氰胺检测中抑制了牛奶干扰,并获得了良好的线性关系(R(2)=0.99)。三聚氰胺碎片谱上的MS/MS 85表明了该方法的选择性。检测限和定量限分别为0.269 µg L(-1)和0.897 µg L(-1)。该方法的回收率和相对标准偏差(RSD)分别低于114%和7.86%。此外,通过红外光谱和显微镜分析对提取物中三聚氰胺的性质进行了进一步研究。沉淀的特征为二水合双(三氯乙酸)三聚氰胺,它是通过三聚氰胺与三氯乙酸相互作用形成氢键而产生的。因此,开发了一种简单、快速且易于操作的三聚氰胺萃取和直接ESI-MS/MS分析方法。