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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Ultrasensitive immunoassay of insulin based on highly efficient electrochemiluminescence quenching of carboxyl-functionalized g-C3N4 through coreactant dual-consumption by NiPd-DNAzyme
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Ultrasensitive immunoassay of insulin based on highly efficient electrochemiluminescence quenching of carboxyl-functionalized g-C3N4 through coreactant dual-consumption by NiPd-DNAzyme

机译:基于高效电化学发光的羧基官能化G-C3N4通过NIPD-DNAzyme的甲基官能化G-C3n4的超敏免疫测定

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摘要

An efficient quenching electrochemiluminescence (ECL) immunosensor for highly sensitive detection of insulin was constructed using carboxyl-functionalized g-C3N4 (C-g-C3N4) as an ECL emitter and hollow NiPd nano particles loading with G-quadruplex/hemin DNAzyme (NiPd-DNAzyme) as the dual-quenching probe. In this protocol, the as-prepared C-g-C3N4 served as both a luminophore and the matrix to immobilize capture antibody (Ab(1)) by amide linkage, which exhibiting strong ECL activity in the presence of the coreactant H2O2. The NiPd showed good peroxidase-activity and loading capacity for both G-quadruplex/hemin DNAzyme and detection antibody (Ab(2)). The dual-peroxidase nature of NiPd-DNAzyme composite highly promoted the reduction of H2O2, resulting in the consumption of the coreactant of C-g-C3N4 and obvious ECL quenching. Using insulin as a model analyte, the change of ECL intensity was logarithmically related to the concentration of the insulin in the range from 0.1 pg.mL(-1) to 20.0 ng.mL(-1) with a detection limit of 33 fg.mL(-1). The wide detection range and high sensitivity resulted from the enhanced ECL emission and highly efficient quenching ability of NiPd-DNAzyme. Furthermore, the ECL immunosensor presented good stability, repeatability and selectivity, which demonstrate that it will be potential in clinical application.
机译:使用羧基官能化的G-C3N4(CG-C3N4)作为ECL发射器和中空NIPD纳米颗粒用G-Quadreplex / Hemin dnazyme(nipd-dnazyme)来构建用于高敏感的胰岛素的高敏感性检测的高敏感性胰岛素的免疫感传感器作为双淬火探针。在该方案中,作为发光体和基质的制备的C-G-C3N4以通过酰胺键固定捕获抗体(AB(1)),其在固件H 2 O 2存在下表现出强烈的ECL活性。 NIPD显示出良好的过氧化物酶活性和G-Quadreplex / Hemin dnazyme和检测抗体的负载能力(Ab(2))。 NIPD-DNAzyme复合材料的双过氧化物酶性质高度促进了H 2 O 2的还原,导致C-G-C3N4的固件消耗和明显的ECL猝灭。使用胰岛素作为模型分析物,ECL强度的变化与0.1pg.ml(-1)至20.0 ng.ml(-1)的范围内的胰岛素的浓度对几乎有关,检测限为33 fg。 ml(-1)。广泛的检测范围和高灵敏度是由于NIPD-DNAzyme的增强的ECL发射和高效猝灭能力导致。此外,ECL免疫传感器呈现出良好的稳定性,可重复性和选择性,表明它将是临床应用的潜力。

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