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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Terbium ion-coordinated carbon dots for fluorescent aptasensing of adenosine 5 '-triphosphate with unmodified gold nanoparticles
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Terbium ion-coordinated carbon dots for fluorescent aptasensing of adenosine 5 '-triphosphate with unmodified gold nanoparticles

机译:ion离子配位碳点与未经修饰的金纳米粒子的荧光修饰5'-三磷酸腺苷

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This work reports on a novel time-resolved fluorescent aptasensing platform for the quantitative monitoring of adenosine 5'-triphosphate (ATP) by interaction of dispersive/agglomerate gold nanoparticles (AuNPs) with terbium ion-coordinated carbon dots (Tb-CDs). To construct such a fluorescent nanoprobe, Tb-CDs with high-efficient fluorescent intensity are first synthesized by the microwave method with terbium ions (Tb3+). The aptasensing system consists of ATP aptamer, AuNP and Tb-CD. The dispersive/agglomerate gold nanoparticles are acquired through the reaction of the aptamer with target ATP. Upon target ATP introduction, the aptamers bind with the analytes to form new aptamer-ATP complexes and coat on the surface of AuNPs to inhibit their aggregation in the high salt solution. In this case, the fluorescent signal of Tb-CDs is quenched by the dispersive AuNPs on the basis of the fluorescence resonance energy transfer (FRET). At the absence of target analyte, gold nanoparticles tend to aggregate in the high salt state even if the aptamers are present. Thus, the added Tb-CDs maintain their intrinsic fluorescent intensity. Experimental results indicated that the aptasensing system exhibited good fluorescent responses toward ATP in the dynamic range from 40 nM to 4.0 mu M with a detection limit of 8.5 nM at 3s(blank) criterion. The repeatability and intermediate precision is less than 9.5% at three concentrations including 0.04, 0.4 and 2.0 mu M ATP. The selectivity was acceptable toward guanosine 5'-triphosphate, uridine 5'-triphosphate and cytidine 5'-triphosphate. The methodology was applied to evaluate the blank human serum spiked with target ATP, and the recoveries (at 3 concentration levels) ranged between 97.0% and 103.7%. Importantly, this detection scheme is rapid, simple, cost-effective, and does not require extensive sample preparation or separation. (C) 2016 Elsevier B.V. All rights reserved.
机译:这项工作报告了一种新型的时间分辨荧光适体平台,该平台通过分散/团聚的金纳米颗粒(AuNP)与b离子配位的碳点(Tb-CD)的相互作用来定量监测5'-三磷酸腺苷(ATP)。为了构建这种荧光纳米探针,首先通过微波法用ter离子(Tb3 +)合成具有高效荧光强度的Tb-CD。适体系统由ATP适体,AuNP和Tb-CD组成。通过适体与靶ATP的反应获得分散/团聚的金纳米颗粒。引入目标ATP后,适体与分析物结合形成新的适体-ATP复合物,并覆盖在AuNP的表面上,以抑制它们在高盐溶液中的聚集。在这种情况下,基于荧光共振能量转移(FRET),Tb-CD的荧光信号被分散的AuNP猝灭。在不存在目标分析物的情况下,即使存在适体,金纳米颗粒也倾向于以高盐态聚集。因此,添加的Tb-CD保持其固有的荧光强度。实验结果表明,在3s(空白)标准下,适体系统在40 nM至4.0μM的动态范围内对ATP表现出良好的荧光反应,检测限为8.5 nM。在包括0.04、0.4和2.0μM ATP的三个浓度下,重复性和中间精度均低于9.5%。对鸟苷5'-三磷酸,尿苷5'-三磷酸和胞苷5'-三磷酸的选择性是可接受的。该方法用于评估掺有目标ATP的空白人血清,回收率(3个浓度水平)在97.0%至103.7%之间。重要的是,该检测方案是快速,简单,具有成本效益的,并且不需要大量的样品制备或分离。 (C)2016 Elsevier B.V.保留所有权利。

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