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Laser induced fluorescence reader for sandwichtype nanoparticle immunoassay to determine salinomycin

机译:激光诱导荧光读取器用于三明治型纳米颗粒免疫测定法测定沙利霉素

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A unique laser-induced fluorescence reader was developed to detect various antibiotics in foods using a sandwich-type immunoassay platform. For the measurement, magnetic nanoparticles (MNPs) were synthesized in the size of 10–20 nm to be used for extraction of antibiotic target by magnetic separation and dye-doped silica nanoparticles (color balls) immobilized with antibody were synthesized in the size of 70–80 nm to be used as a probe for fluorescence detection. The reader system contains a diode laser irradiating from bottom to top for a long cell pathlength. In particular, this system was equipped with a ratiometric supplementary tool in order to compensate the particle loss during the sample pretreatment, which enhanced linearity and reproducibility. When it was demonstrated to determine salinomycin spiked in phosphate buffered saline solutions, detection limit of about <10 pg/mL and excellent linear dynamic range with an improved linearity were obtained. For method and instrumental validation, the result was compared with that of enzyme-linked immunosorbent assay (ELISA). As a result, the developed fluorescence reading system provided a simplified analytical procedure and improved the detection limit more than 100-fold compared to ELISA.
机译:开发了独特的激光诱导荧光读取器,以使用三明治型免疫测定平台检测食品中的各种抗生素。为了进行测量,合成了大小为10–20 nm的磁性纳米颗粒(MNP),用于通过磁分离提取抗生素靶标,并合成了固定有抗体的染料掺杂的二氧化硅纳米颗粒(色球),大小为70 –80 nm用作荧光检测的探针。读取器系统包含一个从底部到顶部照射的二极管激光,用于较长的细胞路径长度。特别是,该系统配备了比例辅助工具,以补偿样品预处理过程中的颗粒损失,从而提高了线性度和可重复性。当证明测定加在磷酸盐缓冲盐溶液中的盐霉素时,检出限约为<10 pg / mL,线性动态范围极佳,线性度得到改善。为了进行方法和仪器验证,将结果与酶联免疫吸附测定(ELISA)进行了比较。结果,与ELISA相比,开发的荧光读取系统提供了简化的分析程序,并将检测限提高了100倍以上。

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