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Gold Nanoparticle Enhanced Electrochemiluminescence of CdS Thin Films for Ultrasensitive Thrombin Detection

机译:金纳米粒子增强CdS薄膜的电化学发光,用于超灵敏的凝血酶检测。

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Interactions between surface plasmons (SP) of metallic surfaces and photoluminescence (PL) of semiconductor nanocrystal (S-NC) surfaces have been extensively investigated, and SP-induced PL enhancement has been used as a sensitive analytical technique. However, this SP induced electrochemiluminescence (ECL) enhancement is rarely studied. In this work, we report greatly enhanced ECL of CdS thin films by gold nanoparticles (Au NPs) for ultrasensitive detection of thrombin. The system was composed of a CdS NC film on glassy carbon electrode (GCE) as ECL emitter attached an aptamer of thrombin. Then, ssDNA-AuNP conjugates hybridized with the aptamer to form a separation length of ca. 12 nm between CdS NCs and Au NPs. The system showed 5-fold enhancement of ECL intensity as compared to that without Au NPs, which might be attributed to the long-distance interaction between the S-NCs and SPR field of noble metal nanoparticles (MNPs). We also found that the enhanced ECL could be influenced by the involving factors such as the separation distance, spectral overlap, and magnetic field. Such enhancement in combination with smart recognition of aptamer and target protein allowed us to construct an ultrasensitive aptasensor for attomolar detection of thrombin. The presence of target protein was reflected by the ECL signal decrease caused by the target-induced removal of ssDNA-AuNP conjugates. The decrease of ECL signal was logarithmically linear with the concentration of thrombin in a wide range from 100 aM to 100 fM. The principle described in this work could be also applied to many other bioassays.
机译:已经广泛研究了金属表面的表面等离子体激元(SP)与半导体纳米晶体(S-NC)表面的光致发光(PL)之间的相互作用,并且SP诱导的PL增强已被用作敏感的分析技术。但是,很少研究这种SP诱导的电化学发光(ECL)增强。在这项工作中,我们报告了金纳米颗粒(Au NPs)对凝血酶的超灵敏检测大大提高了CdS薄膜的ECL。该系统由玻璃碳电极(GCE)上的CdS NC膜组成,该ECL发射器附着了凝血酶的适体。然后,将ssDNA-AuNP缀合物与适体杂交,形成约λ的分离长度。 CdS NC和Au NP之间为12 nm。与没有金纳米颗粒相比,该系统显示出ECL强度提高了5倍,这可能归因于S-NC和贵金属纳米颗粒(MNP)的SPR场之间的长距离相互作用。我们还发现增强的ECL可能受到诸如分离距离,光谱重叠和磁场等相关因素的影响。这种增强与对适体和靶蛋白的智能识别相结合,使我们能够构建一种超灵敏的适体传感器,用于凝血酶的原子摩尔检测。目标蛋白的存在通过目标诱导的ssDNA-AuNP共轭物去除引起的ECL信号降低来反映。 ECL信号的下降与凝血酶的浓度在100 aM至100 fM的宽范围内呈对数线性关系。这项工作中描述的原理也可以应用于许多其他生物测定。

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