Institute of Biotechnology, Department of Microbioanalytics, Faculty of Chemistry, Warsaw University of Technology, Warsaw, Poland.
Anal Bioanal Chem. 2012 Mar;402(7):2259-66. doi: 10.1007/s00216-011-5510-5. Epub 2011 Nov 8.
The feasibility of using gold electrodes modified with short-chain ssDNA oligonucleotides for determination of uranyl cation is examined. Interaction between UO(2)(2+) and proposed recognition layer was studied by means of voltammetric and quartz crystal microbalance measurements. It was postulated that ssDNA recognition layer functions via strong binding of UO(2)(2+) to phosphate DNA backbone. The methylene blue was used as a redox marker for analytical signal generation. Biosensor response was based on the difference in electrochemical signal before and after subjecting it to sample containing uranyl ion. The lower detection limit of 30 nmol L(-1) for UO(2)(2+) was observed for a sample incubation time of 60 min. Proposed ssDNA-modified electrodes demonstrated good selectivity towards UO(2)(2+) against common metal cations, with only Pb(2+) and Ca(2+) showing considerable interfering effect.
研究了使用短链 ssDNA 寡核苷酸修饰的金电极测定铀酰阳离子的可行性。通过伏安法和石英晶体微天平测量研究了 UO(2)(2+)与所提出的识别层之间的相互作用。据推测,ssDNA 识别层通过 UO(2)(2+)与磷酸 DNA 骨架的强结合来发挥作用。亚甲蓝被用作分析信号产生的氧化还原标记物。生物传感器响应基于在将其暴露于含有铀离子的样品前后电化学信号的差异。在样品孵育 60 分钟的情况下,UO(2)(2+)的检测下限低至 30 nmol L(-1)。与常见金属阳离子相比,所提出的 ssDNA 修饰电极对 UO(2)(2+)表现出良好的选择性,只有 Pb(2+)和 Ca(2+)表现出相当大的干扰作用。