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首页> 外文期刊>Sensors and Actuators >Electrochemiluminescence sensing platform for ultrasensitive DNA analysis based on resonance energy transfer between graphitic carbon nitride quantum dots and gold nanoparticles
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Electrochemiluminescence sensing platform for ultrasensitive DNA analysis based on resonance energy transfer between graphitic carbon nitride quantum dots and gold nanoparticles

机译:超敏感性DNA分析的电化学发光性传感平台,基于石墨氮化物量子点和金纳米粒子的共振能量转移

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Electrogenerated chemiluminescence (ECL) of semiconductor quantum dots (QDs) is considered as a powerful technique in the fabrication of biosensor, however, the inherent toxicity of the heavy metal ion containing in QDs limits their further applications. Thus, searching for environment-friendly luminescent nanomaterials with high electrochemiluminescence (ECL) efficiency is an urgent goal. In this work, a solid-state method under low temperature was adopted to prepare graphitic carbon nitride quantum dots (g-CNQDs). By using coreactant K2S2O8, a strong cathodic ECL signal of g-CNQDs could be observed in phosphate buffer. A novel ECL resonance energy transfer procedure was constructed between g-CNQDs (emitter) and gold nanoparticles (acceptor). A signal probe was formed by connecting gold nanoparticles at the hairpin DNA (Hai-DNA) terminal. When the signal probe was anchored on g-CNQDs, ECL resonance energy transfer occurred due to the ECL quenching of gold nanoparticles to g-CNQDs. This phenomenon decreased the ECL signal. In the presence of target DNA (T-DNA), the looped structure of Hai-DNA could be destroyed by T-DNA, and gold nanoparticles were separated from g-CNQDs. Accordingly, the ECL resonance energy transfer procedure was hindered, and the ECL signal was recovered again. The ECL intensities exhibited linear correlation with the logarithm of T-DNA concentration from 0.02 fM to 0.1 pM, and the limit of detection was 0.01 fM (3 sigma). With the developed ECL resonance energy transfer system, good selectivity and high sensitivity were achieved in T-DNA detection.
机译:半导体量子点(QDS)的电化学化学发光(ECL)被认为是在生物传感器的制造中被认为是一种强大的技术,然而,含量在QDS中的重金属离子的固有毒性限制了其进一步的应用。因此,寻找具有高电荧光发光(ECL)效率的环保型发光纳米材料是一种紧急目标。在这项工作中,采用低温下的固态方法制备石墨碳氮化物量子点(G-CNQDS)。通过使用试剂克2S2O8,可以在磷酸盐缓冲液中观察到G-CNQDS的强阴极ECL信号。在G-CNQDS(发射器)和金纳米颗粒(受体)之间构建了一种新的ECL共振能量转移程序。通过将发夹DNA(HAI-DNA)末端的金纳米颗粒连接来形成信号探针。当信号探针锚定在G-CNQD上时,由于金纳米颗粒的ECL猝灭为G-CNQDS,ECL共振能量传递发生。这种现象降低了ECL信号。在靶DNA(T-DNA)的存在下,HI-DNA的环状结构可以通过T-DNA破坏,并且将金纳米颗粒与G-CNQD分离。因此,妨碍了ECL共振能量转移程序,再次回收ECL信号。 ECL强度与0.02 fm至0.1μm的T-DNA浓度的对数表现出线性相关性,并且检测限为0.01 fm(3 sigma)。通过开发的ECL共振能量转移系统,在T-DNA检测中实现了良好的选择性和高灵敏度。

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