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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 >A novel electrochemical method to detect theophylline utilizing silver ions captured within abasic site-incorporated duplex DNA
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A novel electrochemical method to detect theophylline utilizing silver ions captured within abasic site-incorporated duplex DNA

机译:一种利用在无碱基位点结合的双链DNA中捕获的银离子检测茶碱的新型电化学方法

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摘要

We herein describe a novel and label-free electrochemical system to detect theophylline. The system was constructed by immobilizing duplex DNA containing an abasic site opposite cytosine on the gold electrode surface. In the absence of theophylline in a sample, silver ions freely bind to the empty abasic site in the duplex DNA leading to the highly elevated electrochemical signal by the redox reaction of silver ions. On the other hand, when theophylline is present, it binds to the abasic site by pseudo base pairing with the opposite cytosine nucleobase, which consequently prevents silver ions from binding to the abasic site. As a result, redox reaction of silver ions would be greatly reduced resulting in the accordingly decreased electrochemical signal. By employing this electrochemical strategy, theophylline was reliably detected at a concentration as low as 3.2 mu M with the high selectivity over structurally similar substances such as caffeine and theobromine. Finally, the diagnostic capability of this method was also successfully verified by reliably detecting theophylline present in a real human serum sample with an excellent recovery ratio within 100 +/- 6%. (C) 2014 Elsevier B.V. All rights reserved.
机译:我们在本文中描述了检测茶碱的新颖且无标记的电化学系统。该系统是通过在金电极表面上固定一个与胞嘧啶相对的无碱基位点的双链DNA而固定的。在样品中没有茶碱的情况下,银离子可自由结合至双链体DNA中的空无碱基位置,从而通过银离子的氧化还原反应导致高度升高的电化学信号。另一方面,当茶碱存在时,它通过与相对的胞嘧啶核苷碱基的假碱基配对与无碱基结合,从而防止了银离子与无碱基结合。结果,银离子的氧化还原反应将大大降低,从而导致电化学信号相应降低。通过采用这种电化学策略,可可靠地检测到茶碱的浓度低至3.2μM,并且具有比结构类似物质(如咖啡因和可可碱)高的选择性。最后,该方法的诊断能力还通过可靠地检测真人血清样品中存在的茶碱而得到了成功验证,茶碱的回收率在100 +/- 6%之内。 (C)2014 Elsevier B.V.保留所有权利。

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