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Ultra-trace determination of sodium fluoroacetate (1080) as monofluoroacetate in milk and milk powder by GC-MS/MS and LC-MS/MS

机译:用GC-MS / MS和LC-MS / MS超痕量测定牛奶和奶粉中的氟乙酸钠(1080)作为一氟乙酸盐

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A sensitive analytical method based on derivatization with 3-nitroaniline is established for the trace determination of sodium fluoroacetate (1080) in milk and milk powder. The method reported here utilizes protein precipitation with tungstic acid, solid phase extraction (SPE) clean-up in pass-through mode with a mixed-mode anionic exchange (MAX) cartridge and N,N′-dicyclohexylcarbodiimide (DCC) mediated derivatization with 3-nitroaniline (3-NA). The 2-fluoro-N-(3-nitrophenyl)acetamide (MFA–3NA) derivative can be determined with both gas chromatography tandem mass spectrometry (GC-MS/MS) and liquid chromatography tandem mass spectrometry (LC-MS/MS). In our study, negative chemical ionization (NCI) GC-MS/MS and electrospray ionization (ESI) LC-MS/MS in negative ionization mode were used. The quantification of MFA–3NA was accomplished by using matrix-matched calibration with stable isotope labeled sodium monofluoroacetate (13C2D2–MFA) as an internal standard (I.S.). The method was validated with MFA fortified milk samples at 0.1, 0.2 and 0.4 μg L?1 and milk powder samples at 0.5, 1 and 2 μg kg?1. In GC-MS/MS, the LOQs for milk and milk powder samples were 0.0042 μg L?1 and 0.0085 μg kg?1, respectively. The RSDs at all spike levels for milk and milk powder samples were less than 6% with recoveries ranging from 90 to 105%. In LC-MS/MS, the LOQs for milk and milk powder samples were 0.00033 μg L?1 and 0.0088 μg kg?1, respectively. The RSDs at all spike levels for milk and milk powder samples were less than 13% with recoveries ranging from 90 to 112%. The proposed method has been applied to detect 1080 as monofluoroacetate (MFA) in milk and milk powder samples purchased from the local market.
机译:建立了基于3-硝基苯胺衍生化的灵敏分析方法,用于痕量测定牛奶和奶粉中的氟乙酸钠(1080)。本文报道的方法利用钨酸沉淀蛋白质,使用混合模式阴离子交换(MAX)柱以直通模式净化固相萃取(SPE)和N,N'-二环己基碳二亚胺(DCC)介导的3 -硝基苯胺(3-NA)。可以使用气相色谱串联质谱(GC-MS / MS)和液相色谱串联质谱(LC-MS / MS)来确定2-氟-N-(3-硝基苯基)乙酰胺(MFA-3NA)衍生物。在我们的研究中,使用负电离模式下的负化学电离(NCI)GC-MS / MS和电喷雾电离(ESI)LC-MS / MS。使用稳定的同位素标记的单氟乙酸钠(13C2D2-MFA)作为内标(I.S.),通过基质匹配校准完成MFA-3NA的定量。该方法已通过0.1、0.2和0.4μgL?1的MFA强化牛奶样品以及0.5、1和2μgkg?1的奶粉样品进行了验证。在GC-MS / MS中,牛奶和奶粉样品的LOQ分别为0.0042μgL?1和0.0085μgkg?1。牛奶和奶粉样品在所有加标水平下的RSD均低于6%,回收率在90%至105%之间。在LC-MS / MS中,牛奶和奶粉样品的LOQ分别为0.00033μgL?1和0.0088μgkg?1。牛奶和奶粉样品在所有加标水平下的RSD均低于13%,回收率在90%至112%之间。该提议的方法已用于检测从当地市场购买的牛奶和奶粉样品中的1080含量的一氟乙酸盐(MFA)。

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