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首页> 外文期刊>Monatshefte fur Chemie >Photochemically induced fluorimetry, UV-Vis spectroscopy, and voltammetry on the DNA/MWCNT/GCE to investigate the interaction of sulfamethazine with DNA: determination of DNA
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Photochemically induced fluorimetry, UV-Vis spectroscopy, and voltammetry on the DNA/MWCNT/GCE to investigate the interaction of sulfamethazine with DNA: determination of DNA

机译:对DNA / MWCNT / GCE进行光化学诱导荧光分析,UV-Vis光谱和伏安法研究磺胺二甲嘧啶与DNA的相互作用:DNA的测定

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In this study the interaction of sulfamethazine with DNA was investigated by photochemically induced fluorescence, UV-Vis spectroscopy, and voltammetry on the glassy carbon electrode modified with DNA-multiwalled carbon nanotubes composite (DNA/MWCNT/GCE). Photochemically induced fluorescence was based on UV irradiation of sulfamethazine in the presence of sodium sulfite as sensitizing reagent for a fixed time. The photochemically induced fluorescence emitted by sulfamethazine at 348 nm could be quenched in B-R buffer solution (pH 7.0, 0.04 mol dm(-3)) when DNA was added, which indicating the interaction of sulfamethazine with DNA. The mechanism of fluorescence quenching was a static quenching according to the Stern-Volmer plot. Furthermore, interaction of sulfamethazine with DNA on DNA/MWCNT/GCE, showing a decrease of peak current of the sulfamethazine oxidation without significant potential shift. The UV spectroscopic data confirmed the intercalative interaction by hypochromism and bathochromic shift of 242 nm absorbance band. The binding constants of the interaction of sulfamethazine with DNA were obtained by all three methods in the range 1.21 x 10(3)-2.2 x 10(3) dm(3) mol(-1). Finally, photochemically induced fluorescence was successfully applied for determination of DNA with satisfactory linearity ranges (0.7-8.1 and 13.1-65.0 mg dm(-3)), admissible limit of detection (0.43 mg dm(-3)), and good repeatability (0.29 %).
机译:在这项研究中,通过光化学诱导的荧光,UV-Vis光谱和伏安法研究了磺胺二嗪与DNA的相互作用,该电极由DNA-多壁碳纳米管复合物(DNA / MWCNT / GCE)修饰。光化学诱导的荧光是基于磺胺二甲基嘧啶在亚硫酸钠作为敏化剂存在下经过固定时间的紫外线照射。当添加DNA时,磺胺二甲基嘧啶在348 nm处发出的光化学诱导荧光可以在B-R缓冲溶液(pH 7.0,0.04 mol dm(-3))中淬灭,这表明磺胺二甲基嘧啶与DNA相互作用。根据Stern-Volmer图,荧光猝灭的机理是静态猝灭。此外,磺胺二甲嘧啶与DNA / DNA / MWCNT / GCE上的DNA相互作用,显示磺胺二甲嘧啶氧化的峰值电流降低而没有明显的电势漂移。紫外光谱数据证实了低色度和242 nm吸收带的红移引起的嵌入相互作用。通过所有三种方法在1.21 x 10(3)-2.2 x 10(3)dm(3)mol(-1)范围内获得磺胺二甲嘧啶与DNA相互作用的结合常数。最后,将光化学诱导的荧光成功地用于测定具有令人满意的线性范围(0.7-8.1和13.1-65.0 mg dm(-3)),允许的检出限(0.43 mg dm(-3))和良好的重复性的DNA测定。 0.29%)。

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