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A Label-free Cardiac Troponin T Electrochemiluminescence Immunosensor Enhanced by Graphene Nanoplatelets

机译:由石墨烯纳米孔增强的无标记心肌发光器免疫传感器免疫传感器

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摘要

In this study, a direct and label-free immunosensor was designed and constructed by modifying the screen-printed electrode with graphene nanoplatelets (GNPs) for the detection of the cardiac troponin T (cTnT). Firstly, GNPs were drop-casted onto carbon working electrode. Monoclonal cTnT antibodies were then immobilized on the GNPs via physical adsorption; finally, BSA was introduced to block non-specific binding sites. The detection of cTnT was performed using an electrochemiluminescence (ECL) technique with tris(bipyridine)ruthenium(II) chloride ([Ru(bpy)_(3)]Cl_(2)) used as a luminophore and TPrA (tripropylamine) as a co-reactant. The ECL intensity was demonstrated to be directly proportional to the cTnT concentration where a linear range from 100 pg mL~(?1) to 5 fg mL~(?1) of the cTnT detection was established. An extremely low limit of detection was achieved to be 0.05 fg mL~(?1) with an outstanding specificity. Additionally, this immunosensor showed excellent percentage recovery for real samples analyses in artificially spiked human serum.
机译:在该研究中,通过用石墨烯纳米片(GNP)改变丝网印刷电极来设计和构建直接和无标记免疫传感器,用于检测心肌肌钙蛋白T(CTNT)。首先,将GNP丢弃到碳工作电极上。然后通过物理吸附将单克隆CTNT抗体固定在GNPSβ上;最后,引入BSA以阻断非特异性结合位点。使用具有Tris(Bi0 yridine)钌(II)氯化钌(II)的电化学发光(ECL)技术进行CTNT的检测([Ru(BPY)_(3)] Cl_(2))用作发光体和TPRA(三丙胺)作为a共反应物。 ECL强度被证明与CTNT浓度成比例,其中建立了CTNT检测的100pg ml〜(α1)至5fg ml〜(α1)的线性范围。具有出色的特异性的0.05fg ml〜(α1)的极低检测限。另外,这种免疫传感器显示出优异的百分比恢复,用于人工尖刺的人血清中的真实样品分析。

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