Application of Time-resolved Fluroimmunoassay for Determination of Furaltadone Metabolite 3-Amino-5-morpholinomethyl-2-oxazolidinone

Application of Time-resolved Fluroimmunoassay for Determination of Furaltadone Metabolite 3-Amino-5-morpholinomethyl-2-oxazolidinone
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应用时间分辨荧光免疫分析法测定呋喃他酮代谢物3-氨基-5-吗啉甲基-2-恶唑烷酮

DOI:
10.1016/s1872-2040(16)60951-9
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发表时间:
2016-08-01
影响因子:
1.2
通讯作者:
Shen Yu-Dong
Shen Yu-Dong
中科院分区:
化学4区
文献类型:
--
作者:
Deng Li-Hua;Dai Jin-Bo;Shen Yu-Dong

文献摘要

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为检测鱼类样品中呋喃他酮代谢产物3-氨基-5-吗啉甲基-2-恶唑烷酮(AMOZ),建立了Eu~(3+)标记时间分辨荧光免疫分析方法。优化的实验条件为:AMOZA-OVA浓度为0.25ug·mL~(-1),抗体稀释50000倍,竞争反应时间为50min。在最佳条件下,该方法的检出限为0.01ngmL(-1),IC_(50)为0.26ngmL(-1),线性范围(IC20~IC80)为0.025~2.83ngmL(-1)。在3个添加水平下,鱼中Amoz的加标回收率为78.0%~86.0%,相对标准偏差小于15%。IC-TRFIA与高效液相色谱-串联质谱仪对添加食品样品的分析结果具有良好的相关性。所建立的IC-TRFIA方法适用于食品样品中氨甲肼残留量的测定。
To detect furaltadone metabolite 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) in fish sample, a Eu3+ labeling time-resolved fluoroimmunoassay (TRFIA) was developed. The experimental conditions were optimized as follows: the AMOZA-OVA concentration was 0.25 mu g mL(-1); the antibody was diluted by 50000 folds, and the competitive reaction time was 50 min. Under the optimal conditions, the method showed a detection limit of 0.01 ng mL(-1), an IC50 of 0.26 ng mL(-1) and a linear range (IC20-IC80) of 0.025-2.83 ng mL(-1). The spiked recoveries of AMOZ in fish at three spiked levels ranged from 78.0% to 86.0%, and the relative standard deviations were less than 15%. Good correlation between ic-TRFIA and high performance liquid chromatography-tandem mass spectrometry was obtained for spiked food samples. The proposed ic-TRFIA method was suitable for the determination of AMOZ residue in food samples.