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使用液相色谱-串联质谱法测定和确证蜂蜜中的硝基呋喃残留量。

Determination and confirmation of nitrofuran residues in honey using LC-MS/MS.

作者信息

Lopez Mayda I, Feldlaufer Mark F, Williams Anthony D, Chu Pak-Sin

机构信息

Center for Veterinary Medicine, U.S. Food and Drug Administration, 8401 Muirkirk Road, Laurel, MD 20708, USA.

出版信息

J Agric Food Chem. 2007 Feb 21;55(4):1103-8. doi: 10.1021/jf0625712. Epub 2007 Jan 25.

Abstract

A method was developed for the determination and confirmation of furazolidone, nitrofurazone, furaltadone, and nitrofurantoin as their side-chain residues in honey using liquid chromatography-tandem mass spectrometry (LC-MS/MS). An initial solid-phase extraction cleanup of the honey samples was followed by overnight hydrolysis and derivatization of the nitrofuran side-chain residues with 2-nitrobenzaldehyde. After pH adjustment and liquid-liquid extraction, the extracts were assayed by LC-MS/MS using electrospray ionization in the positive ion mode. The method was validated at concentrations ranging from 0.5 to 2.0 ppb with accuracies of 92-103% and coefficients of variation of < or =10%. The lowest calibration standard used (0.25 ppb) was defined as the limit of quantitation for all four nitrofuran side-chain residues. The extracts and standards were also used for confirmatory purposes. Honey from dosed beehives was assayed to study the stability of the nitrofuran residues and to demonstrate the effectiveness of the method.

摘要

建立了一种使用液相色谱 - 串联质谱法(LC-MS/MS)测定和确证蜂蜜中呋喃唑酮、呋喃西林、呋哺它酮和呋喃妥因及其侧链残留量的方法。首先对蜂蜜样品进行固相萃取净化,然后对硝基呋喃侧链残留进行过夜水解并用2-硝基苯甲醛衍生化。调节pH值并进行液 - 液萃取后,采用电喷雾电离正离子模式通过LC-MS/MS对提取物进行分析。该方法在0.5至2.0 ppb的浓度范围内进行了验证,准确度为92 - 103%,变异系数≤10%。所用的最低校准标准品(0.25 ppb)被定义为所有四种硝基呋喃侧链残留的定量限。提取物和标准品也用于确证目的。对投喂过药物的蜂箱所产蜂蜜进行分析,以研究硝基呋喃残留的稳定性并证明该方法的有效性。

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