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Development of a Cyclic Voltammetry Method for DNA Electrochemical Detection on Microfluidic Gene Chip

机译:微流控基因芯片上DNA电化学检测的循环伏安法开发

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On the microfluidic gene chip, due to high difficulty in temperature changes frequently and productsdetecting equipment miniaturize, the conventional methods of DNA detection can meet therequirements. In this paper, a newly electrochemical method, cyclic voltammetry, basing on a set ofspecial electrodes and the Loop-mediated isothermal amplification (LAMP), was introduced. TheDNA amplification products of LAMP could be combined with the positive dye (Methylene blue),which leading to a reduction in the oxidation peak current (ipA) and reduction peak current (ipC) ofthe cyclic voltammetry. The changes of ipA/ipC were real-time measured by the special electrodes, sothe copies of DNA were quantitative detected. The results show that it could be completed in 300-1 minutes with the lowest DNA to 10 CFU.mL , with high accuracy (96.5%), high sensitivity (96.0%),high specificity (97.0%) compare to the PCR, and good anti-interference ability against Vitamin C (up-1 -1 to 32mg.L ) and Aspirin (up to 64mg.L ) within the sample. Therefore, it was a rapid, sensitive andstable method of DNA detection, has great potential in applying on the microfluidic gene chips.
机译:在微流控基因芯片上,由于温度变化的难度较大,产品检测设备小型化,常规的DNA检测方法可以满足要求。本文介绍了一种基于一组特殊电极和环介导的等温扩增(LAMP)的电化学新方法,循环伏安法。 LAMP的DNA扩增产物可以与正染料(亚甲基蓝)结合使用,从而导致循环伏安法的氧化峰电流(ipA)和还原峰电流(ipC)降低。通过专用电极实时测量ipA / ipC的变化,从而定量检测DNA的拷贝。结果表明,与PCR相比,可在300-1分钟内完成,DNA最低至10 CFU.mL,具有较高的准确性(96.5%),高灵敏度(96.0%),高特异性(97.0%),并且对样品中的维生素C(高达-1 -1至32mg.L)和阿司匹林(高达64mg.L)具有良好的抗干扰能力。因此,它是一种快速,灵敏,稳定的DNA检测方法,在微流控基因芯片上具有广阔的应用前景。

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