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首页> 外文期刊>Journal of the Serbian Chemical Society >Polarographic determination of DNA based on its interaction with the phenanthroline-zinc(II) complex
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Polarographic determination of DNA based on its interaction with the phenanthroline-zinc(II) complex

机译:极谱法根据其与菲咯啉-锌(II)配合物的相互作用进行测定

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By using the linear sweep voltammetric technique, a phenanthroline (Phen) and zinc(II) (Phen-Zn(II)) complex was used as the electrochemical probe for the determination of double-stranded (ds) DNA. In pH 9.0 Britton- -Robinson (B-R) buffer solution, Phen can interact with Zn(II) to form a stable electroactive [Phen-Zn(II)] complex, which had a sensitive second order derivative polarographic reductive peak at -1.300 V (vs. SCE). After the addition of dsDNA into a solution of Phen-Zn(II) complex, the reduction peak current decreased with a negative shift of the reduction peak potential and without the appearance of new peaks. The results showed that a new supramolecular complex was formed via interaction of the Phen-Zn(II) complex with dsDNA. The conditions of interaction and the electrochemical detection were carefully investigated. Under the optimum conditions, the decrease in the reduction peak current was directly proportional to the dsDNA concentration in the range of 0.4-18.0 mg L-1 with the linear regression equation: ΔIp″A = 349.48 + + 84.647(c/mg L-1) (n = 13, γ = 0.991) and a determination limit of 0.20 mg L-1 (3σ). The relative standard deviation (RSD) for 10 parallel determinations of 10.0 mg L-1 dsDNA was found to be 2.03 %. The method was successfully applied to the detection of synthetic samples with satisfactory results.
机译:通过使用线性扫描伏安法,将菲咯啉(Phen)和锌(II)(Phen-Zn(II))络合物用作电化学探针,用于测定双链(ds)DNA。在pH 9.0的Britton--Robinson(BR)缓冲溶液中,Phen可以与Zn(II)相互作用形成稳定的电活性[Phen-Zn(II)]络合物,该络合物在-1.300 V处具有敏感的二阶导数极谱还原峰。 (相对于SCE)。将dsDNA添加到Phen-Zn(II)配合物溶液中后,还原峰电流降低,还原峰电位为负值,并且不会出现新峰。结果表明,Phen-Zn(II)配合物与dsDNA相互作用形成了新的超分子配合物。仔细研究了相互作用的条件和电化学检测。在最佳条件下,还原峰电流的减少与dsDNA浓度在0.4-18.0 mg L-1范围内成正比,线性回归方程为:ΔIp''/ nA = 349.48 + + 84.647(c / mg L -1)(n = 13,γ= 0.991),测定极限为0.20 mg L-1(3σ)。 10次​​平行测定10.0 mg L-1 dsDNA的相对标准偏差(RSD)为2.03%。该方法成功应用于合成样品的检测,结果令人满意。

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