首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Sandwich immunoassay for alpha-fetoprotein in human sera using gold nanoparticle and magnetic bead labels along with resonance Rayleigh scattering readout
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Sandwich immunoassay for alpha-fetoprotein in human sera using gold nanoparticle and magnetic bead labels along with resonance Rayleigh scattering readout

机译:使用金纳米颗粒和磁珠标签以及共振瑞利散射读数对人血清中甲胎蛋白的夹心免疫测定

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摘要

We describe a sensitive sandwich immunoassay for alpha-fetoprotein (AFP). It is making use of gold nanoparticles (GNPs) and magnetic beads (MBs) as labels, and of resonance Rayleigh scattering for detection. Two antibodies were labeled with GNPs and MBs, respectively, and MB-antigen-GNP complexes were formed in the presence of antigens. The MB labels also serve as solid phase carriers that can be used to magnetically separate the immuno complex. The GNP labels are used as optical probes, and Rayleigh scattering was used to determine the concentration of free GNPs-antibody after separation of the MB-antigen-GNP complexes. The concentration of AFP is related to the intensity of light scattered by free GNPs in the 13.6 pM to 436 pM concentration range, and the limit of detection is 13.6 pM. The method was apphed to the determination of AFP in sera of cancer patients, and the resufts agree well with those obtained by conventional ELISA.
机译:我们描述了针对甲胎蛋白(AFP)的灵敏夹心免疫分析法。它利用金纳米颗粒(GNP)和磁珠(MB)作为标记,并利用共振瑞利散射进行检测。两种抗体分别用GNPs和MBs标记,并且在抗原存在下形成MB-抗原-GNP复合物。 MB标记物也可用作固相载体,可用于磁性分离免疫复合物。 GNP标记用作光学探针,瑞利散射用于确定MB-抗原-GNP复合物分离后游离GNPs-抗体的浓度。 AFP的浓度与浓度在13.6 pM至436 pM范围内的游离GNP散射的光的强度有关,检测极限为13.6 pM。该方法适用于癌症患者血清中AFP的测定,结果与常规ELISA法测定结果吻合良好。

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