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 >A novel and sensitive electrogenerated chemiluminescence biosensor for detection of p16(INK4a) gene based on the functional paste-like nanofibers composites-modified screen-printed carbon electrode
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A novel and sensitive electrogenerated chemiluminescence biosensor for detection of p16(INK4a) gene based on the functional paste-like nanofibers composites-modified screen-printed carbon electrode

机译:基于功能糊状纳米纤维复合材料改性丝网印刷碳电极的新型和敏感的电化学化学发光生物传感器,用于检测P16(INK4A)基因的P16(INK4A)基因

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摘要

In this work, we offered a novel and sensitive electrogenerated chemiluminescence (ECL) biosensing system for detection of p16(INK4a )gene using the functional paste-like nanofibers composites-modified screen-printed carbon electrode (SPCE). The paste-like nanofibers composites (PG/GR/CS) which were comprised of the electrospun nanofibers (PG, the graphene (GR) doped polycaprolactam 6 (PA6) were prepared via one-step electrospinning), graphene (GR) and chitosan (CS) were served as the nanosized backbones for pyrrole (Py) electropolymerization. The functional paste-like nanofibers composites (PG/GR/CS/PPy) used as a substrate for dsDNA (hybridization reaction of ssDNA1, p16(INK4a) gene and the Ru(bpy)(3)(2+)/silver nanoparticles (AgNPs) doped gold (Au) core-shell luminescent composite nanoparticles labeled ssDNA2 (RuAg@AuNPs-ssDNA2)) immobilization. Under optimal conditions, a linear relationship between ECL intensity and p16(INK4a )gene concentration was found in a range of 0.1 pM-1 nM with the detection limit of 0.05 pM (S/N = 3). This ECL biosensor based on the PG/GR/CS/PPy-modified SPCE demonstrated excellent electrochemical performance for the detection of p16(INK4a) gene and this platform can be used for the determination of various analytes.
机译:在这项工作中,我们使用提供了一个新颖的和敏感的电致化学发光(ECL)的生物传感系统,用于检测p16蛋白(INK4A)基因的功能糊状纳米纤维复合材料改性的丝网印刷碳电极(SPCE)。该糊一样,其被包含在电纺纳米纤维(PG,掺杂的聚己内酰胺6(PA6)制备通过一步法静电石墨烯(GR)),石墨烯(GR)和脱乙酰壳多糖的纳米纤维复合材料(PG / GR / CS)( CS)分别担任了吡咯(PY)电解的纳米骨干。功能糊状用作底物为双链DNA(和p16(INK4A)基因和吡啶钌(3)(2 +)/银纳米颗粒ssDNA1的杂交反应(纳米纤维的复合材料(PG / GR / CS / PPY)的AgNPs)掺杂金(Au)核 - 壳发光复合纳米颗粒标记的ssDNA2(RUAG @金纳米-ssDNA2))固定化。在最佳条件下,发光强度和p16(INK4A)基因浓度之间的线性关系与的下午12点05(S / N = 3)检测极限的范围为0.1 PM-1纳米的被发现。此ECL生物传感器基于所述PG / GR / CS /聚吡咯改性SPCE表现出了优异的电化学性能,用于检测p16基因(INK4A)基因和该平台可以用于各种分析物的确定。

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