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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Triple signal amplification using gold nanoparticles, bienzyme and platinum nanoparticles functionalized graphene as enhancers for simultaneous multiple electrochemical immunoassay
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Triple signal amplification using gold nanoparticles, bienzyme and platinum nanoparticles functionalized graphene as enhancers for simultaneous multiple electrochemical immunoassay

机译:使用金纳米颗粒,双酶和铂纳米颗粒功能化的石墨烯作为增强剂的三重信号放大,可同时进行多个电化学免疫测定

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摘要

Here we demonstrated an ultrasensitive electrochemical immunoassay employing graphene, platinum nanoparticles (PtNPs), glucose oxidase (GOD) and horseradish peroxidase (HRP) as enhancers to simultaneously detect carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP). This immunosensor is based on the observation that multiple-labeled antibodies (thionine-labeled anti-CEA and ferrocene-labeled anti-AFP) recognition event yielded a distinct voltammetric peak through "sandwich" immunor-eaction, whose position and size reflected the identity and level of the corresponding antigen. Greatly enhanced sensitivity for cancer markers is based on a triple signal amplification strategy. Experimental results revealed that the immunoassay enabled simultaneous determination of CEA and AFP in a single run with wide working ranges of 0.01-100 ng mL~(_1). The detection limits reached 1.64 pg mL~(_1) for CEA and 1.33 pg mL~(_1) for AFP. No obvious cross-talk was observed during the experiment. In addition, through the analysis of clinical serum samples, the proposed method received a good correlation with ELISA as a reference. The signal amplification strategy could be easily modified and extended to detect other multiple targets.
机译:在这里,我们展示了一种超灵敏的电化学免疫测定方法,采用石墨烯,铂纳米颗粒(PtNPs),葡萄糖氧化酶(GOD)和辣根过氧化物酶(HRP)作为增强剂,可同时检测癌胚抗原(CEA)和甲胎蛋白(AFP)。此免疫传感器基于以下观察结果:通过“三明治”免疫反应,多重标记的抗体(蛋氨酸标记的抗CEA和二茂铁标记的抗AFP)识别事件产生了一个明显的伏安峰,其位置和大小反映了身份和相应抗原的水平。基于三重信号放大策略,大大提高了对癌症标记物的敏感性。实验结果表明,该免疫分析法能够在0.01-100 ng mL〜(_1)的宽工作范围内一次运行同时测定CEA和AFP。 CEA的检出限达到1.64 pg mL〜(_1),AFP的检出限达到1.33 pg mL〜(_1)。实验期间未观察到明显的串扰。此外,通过对临床血清样品的分析,该方法与以ELISA为参考的方法具有良好的相关性。信号放大策略可以轻松修改和扩展,以检测其他多个目标。

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