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Simultaneous detection of dual proteins using quantum dots coated silica nanoparticles as labels

机译:使用量子点包被的二氧化硅纳米颗粒作为标记物同时检测双重蛋白质

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摘要

Simultaneous detection of multianalytes associated with a particular cancer is beneficial for disease diagnosis. Here, a facile immunosensing strategy was designed to allow simultaneous electrochemical detection of dual proteins, in a single run. CdSe and PbS water-soluble quantum dots (QDs) were prepared and coated on monodisperse silica nanoparticles as labels for proteins detection. Rabbit immunoglobulin G antigen (IgG) and carcinoembryonic antigen (CEA) were chosen as model proteins for analysis. After a typical sandwich immunoassay, CdSe and PbS QDs labels were introduced onto the Au substrates' surface, which were then dissolved and could be simultaneously monitored by square-wave-voltammetric (SWV) stripping measurements. Under selected conditions, IgG and CEA could be assayed in the ranges of 0.05-40ngmL~(-1) and 0.05-25ngmL~(-1), respectively. The proposed method possessed high sensitivity, good precision, and satisfactory reproducibility and regeneration.
机译:同时检测与特定癌症相关的多种分析物对于疾病诊断是有益的。在这里,设计了一种简便的免疫传感策略,可以在一次运行中同时电化学检测双重蛋白质。制备CdSe和PbS水溶性量子点(QDs),并涂覆在单分散二氧化硅纳米颗粒上,作为蛋白质检测的标记。选择兔免疫球蛋白G抗原(IgG)和癌胚抗原(CEA)作为模型蛋白进行分析。经过典型的夹心免疫测定后,将CdSe和PbS QDs标签引入到Au底物的表面上,然后将其溶解,并可以通过方波伏安(SWV)溶出测量同时进行监测。在选定的条件下,可分别在0.05-40ngmL〜(-1)和0.05-25ngmL〜(-1)范围内测定IgG和CEA。该方法灵敏度高,精密度好,重现性和再生性好。

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