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Nitrogen-doped Carbon Dots Mediated Fluorescent on-off Assay for Rapid and Highly Sensitive Pyrophosphate and Alkaline Phosphatase Detection

机译:氮掺杂碳点介导的荧光开-关分析用于快速高灵敏度的焦磷酸和碱性磷酸酶检测。

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摘要

In this report, a novel fluorescent sensing platform using nitrogen-doped carbon dots (N-CDs) as probes for fluorescence signal transmission has been designed for the detection of significant biomolecules pyrophosphate (PPi) and alkaline phosphatase (ALP). The high fluorescent N-CDs could be selectively quenched by Cu2+, and recovered by the addition of PPi because PPi preferentially binds to Cu2+. Once ALP was introduced into the system, ALP can specifically hydrolyze PPi into Pi, the intense fluorescence of N-CDs could be quenched again due to the recombination of the as-released Cu2+ with N-CDs. So, fluorescence of N-CDs is regulated by an ALP-triggered reaction. Based on this strategy, we demonstrated that N-CDs could serve as a very effective fluorescent sensing platform for label-free, sensitive and selective detection of PPi and ALP with low detection limit of 0.16 μM and 0.4 U/L for PPi and ALP, respectively. Moreover, the assay time is just around 0.5 min for PPi and 30 min for ALP. This developed strategy shows remarkable advantages including sensitive, rapid, simple, convenient, and low-cost and so forth. Furthermore, this method was also successfully applied to monitor ALP in human serum, which indicates its great potential for practical applications in biological and clinical diagnosis.
机译:在本报告中,已设计了一种使用氮掺杂碳点(N-CD)作为荧光信号传输探针的新型荧光传感平台,用于检测重要的生物分子焦磷酸(PPi)和碱性磷酸酶(ALP)。高荧光N-CDs可以被Cu 2 + 选择性淬灭,并通过添加PPi来回收,因为PPi优先与Cu 2 + 结合。将ALP引入系统后,ALP可以将PPi特异性水解为Pi,由于释放的Cu 2 + 与N-CD的重组,N-CD的强烈荧光可能会再次被淬灭。 。因此,N-CD的荧光受ALP触发的反应调节。基于此策略,我们证明了N-CD可以作为无标记,灵敏和选择性检测PPi和ALP的非常有效的荧光传感平台,其检测限低至0.16μm和0.4iU / L(PPi和ALP),分别。而且,PPi和ALP的检测时间仅为0.5µmin,大约30µmin。这种发达的策略显示出显着的优势,包括灵敏,快速,简单,方便和低成本等。此外,该方法还成功地用于监测人血清中的ALP,这表明其在生物学和临床诊断中的实际应用具有巨大潜力。

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