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An immunomagnetic separation based fluorescence immunoassay for rapid myoglobin quantification in human blood

机译:基于免疫磁分离的荧光免疫测定法可快速定量人血中的肌红蛋白

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摘要

Magnetic nanoparticle (NPs) and fluorescent NP pairs were designed for myoglobin (Myo) detection in human blood. Magnetic NPs MNP@SiO2@BSA@Au with about 200 nm diameter (by TEM) were prepared through a layer by layer technique following by adsorption of anti-Myo antibody 4E2 on a Au surface. The MNPs were well dispersed in an aqueous solution. Fluorescent NPs were prepared by conjugating fluorescent Rhodamine Red-X (RhX) and another Myo antibody 7C3 on silica NPs with a final diameter of 80 nm. In the presence of Myo, magnetic NPs bearing 4E2 and fluorescent NPs bearing 7C3 form a sandwich structure, which can be separated from blood under a magnetic field. The concentration of Myo is quantified by the fluorescence intensity of SNP@RhX NPs in the sandwich structure. The calibration curve of the Myo showed a linear range between 0 and 250 ng mL(-1) (R-2 = 0.993). The minimum detectable concentration was 0.28 ng mL(-1). The immunomagnetic separation based fluorescence immunoassay offered a simple and accurate way to determine Myo in human blood in 30 min.
机译:磁性纳米颗粒(NPs)和荧光NP对设计用于检测人血中的肌红蛋白(Myo)。通过将抗Myo抗体4E2吸附在Au表面上,通过逐层技术制备具有约200nm直径的磁性NP MNP @ SiO2 @ BSA @ Au。 MNP很好地分散在水溶液中。通过在最终直径为80 nm的二氧化硅NP上缀合荧光若丹明Red-X(RhX)和另一种Myo抗体7C3来制备荧光NP。在存在Myo的情况下,带有4E2的磁性NP和带有7C3的荧光NP形成三明治结构,可以在磁场下与血液分离。 Myo的浓度由三明治结构中SNP @ RhX NP的荧光强度定量。 Myo的校准曲线显示了0到250 ng mL(-1)之间的线性范围(R-2 = 0.993)。最低可检测浓度为0.28 ng mL(-1)。基于免疫磁分离的荧光免疫测定法提供了一种简单而准确的方法,可在30分钟内测定人血中的Myo。

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