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纳米环氨基功能化磁性聚合物分散微固相萃取与超快速液相色谱-串联质谱联用技术在奶粉中双氰胺残留分析中的应用

Application of nanoring amino-functionalized magnetic polymer dispersive micro-solid-phase extraction and ultra fast liquid chromatography-tandem mass spectrometry in dicyandiamide residue analysis of powdered milk.

作者信息

Chen Xiao-Hong, Zhou Li-Xin, Zhao Yong-Gang, Pan Sheng-Dong, Jin Mi-Cong

机构信息

Zhejiang Provincial Key Laboratory of Health Risk Appraisal for Trace Toxic Chemicals, Ningbo Municipal Center for Disease Control and Prevention, Ningbo, Zhejiang 315010, China; Ningbo Key Laboratory of Poison Research and Control, Ningbo Municipal Center for Disease Control and Prevention, Ningbo, Zhejiang 315010, China.

Medical School, Ningbo University, Ningbo, Zhejiang 315211, China.

出版信息

Talanta. 2014 Feb;119:187-92. doi: 10.1016/j.talanta.2013.10.003. Epub 2013 Nov 8.

Abstract

In this study, a rapid and accurate ultra-fast liquid chromatography-tandem quadrupole mass spectrometry (UFLC-MS/MS) method combined with dispersive micro-solid-phase extraction (d-µ-SPE) using a core-shell nanoring amino-functionalized magnetic polymer (CS-NR-MP) was established and validated to determine trace dicyandiamide (DCD) in powdered milk. The developed d-µ-SPE cleanup procedure can dramatically reduce the matrix in samples, and lead to a significant reduction in absolute matrix effects. Chromatographic separation was performed on an Acquity UPLC BEH Amide column by using water-acetonitrile (9:91, v/v) as the mobile phase within 2 min. DCD was quantitatively analyzed by using DCD-(15)N2(13)C2 as an internal standard. The results showed that the recoveries were between 99.8 and 105.6% with RSDs in the range of 0.5-4.9%. The target compound had good linearity in the range of 0.1-20.0 µg L(-1) with a correlation coefficient (r) of 0.9996. The limit of quantification (LOQ) was 0.06 µg kg(-1). This method can be used for the rapid and sensitive determination of ultratrace DCD residue in powdered milk samples.

摘要

本研究建立并验证了一种快速准确的超快速液相色谱 - 串联四极杆质谱法(UFLC-MS/MS),该方法结合了使用核壳纳米环氨基功能化磁性聚合物(CS-NR-MP)的分散微固相萃取(d-µ-SPE),用于测定奶粉中的痕量双氰胺(DCD)。所开发的d-µ-SPE净化程序可显著减少样品中的基质,并导致绝对基质效应显著降低。在Acquity UPLC BEH酰胺柱上进行色谱分离,以水 - 乙腈(9:91,v/v)为流动相,在2分钟内完成分离。以DCD-(15)N2(13)C2作为内标对DCD进行定量分析。结果表明,回收率在99.8%至105.6%之间,相对标准偏差(RSD)在0.5%至4.9%范围内。目标化合物在0.1 - 20.0 µg L(-1)范围内具有良好的线性,相关系数(r)为0.9996。定量限(LOQ)为0.06 µg kg(-1)。该方法可用于快速灵敏地测定奶粉样品中的超痕量DCD残留。

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