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Liquid Chromatography-Tandem Mass Spectrometry for the Determination of Protein-Bound Residues in Shrimp Dosed with Nitrofurans

机译:液相色谱-串联质谱法测定硝基呋喃对虾中蛋白质结合的残留量

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An analytical method was developed for the determination of bound residues of the nitrofuran drugs furazolidone,nitrofurazone,furaltadone,and nitrofurantoin with a sensitivity of 1 ppb in shrimp.In this procedure,shrimp tissue is prewashed with solvents followed by overnight acid hydrolysis,during which the side chains of the bound residues are released and simultaneously derivatized with 2-nitrobenzaldehyde.After liquid-liquid extraction cleanup,the derivatives are detected and quantitated using liquid chromatography-mass spectrometry/mass spectrometry(LC-MS/MS)with an atmospheric pressure chemical ionization interface.The method was validated using control shrimp fortified with each side-chain analyte at 1,2,and 4 ppb.Method accuracies were >80% with coefficients of variation of <20% for all four analytes.Tissues from dosed shrimp were assayed to demonstrate the effectiveness of the method for recovering bound residues of nitrofurans.In shrimp dosed with nitrofurans,nitrofurantoin exhibited the lowest level of bound residues.
机译:建立了一种分析方法,用于测定虾中硝基呋喃药物呋喃唑酮,硝基呋喃酮,呋喃他酮和呋喃妥因的结合残留物,灵敏度为1 ppb。在此程序中,将虾组织用溶剂预洗,然后进行过夜酸水解,在此过程中释放出结合残基的侧链,并同时用2-硝基苯甲醛衍生。液-液萃取净化后,使用大气压液相色谱-质谱/质谱(LC-MS / MS)对衍生物进行检测和定量。化学电离界面。该方法通过使用分别以1,2和4 ppb的每个侧链分析物强化的对虾进行验证,方法准确度> 80%,所有四种分析物的变异系数均<20%。进行了测定,以证明该方法对回收硝基呋喃的残留残留物的有效性。抑制了最低水平的结合残基。

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