Establishment of Chemiluminescent Enzyme Immunoassay for Determination of Amantadine Residues
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摘要: 建立金刚烷胺残留的化学发光酶免疫方法。对酶标抗原与磁标抗体的最佳稀释倍数、反应时间、底物发光时间进行优化,建立标准曲线,同时对方法的检测限、准确度和精密度进行评价。结果表明:50%抑制浓度(IC50)为0.481 μg/L,线性范围是0.085~2.729 μg/L;在动物组织、兽药、饲料中的检测限为0.1 μg/kg,样本添加回收率为80.2%~94.5%,批内、批间相对标准偏差均<10%。该方法灵敏度高、操作简便,可广泛用于动物组织、兽药、饲料中金刚烷胺残留量的测定。Abstract: The aim of the study is to establish a method for determination of amantadine residues by chemiluminescent enzyme immunoassay (CLEIA). After optimizing the dilution multiple of enzyme-labeled antigen and magnetic labeled antibody, reaction time and substrate luminescence time, a standard curve was established, and finally the detection limit, accuracy and precision of the method were evaluated. The results showed that the 50% inhibitory concentration (IC50) was 0.481 μg/L, and the linearity range was 0.085~2.729 μg/L. The detection limit in animal tissues, veterinary drugs and feed were 0.1 μg/kg. The recoveries ranged from 80.2%~94.5%, with the intra-assay and inter-assay coefficients of variation less than 10%. The method is sensitive, simple and it can be widely used for the determination of amantadine residues in animal tissues, veterinary drugs and feed.
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Keywords:
- amantadine /
- chemiluminescent enzyme immunoassay /
- animal tissues /
- veterinary drugs /
- feed
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