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Syntheses, spectroscopic characterization and application to DNA determination of novel fluorescent pyridophenazine derivatives

机译:新型荧光吡啶并吩嗪衍生物的合成,光谱表征及在DNA测定中的应用

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摘要

A series of pyridophenazine derivatives were synthesized and characterized as DNA intercalating fluo-rophores. These pyridophenazines showed absorption maxima at ca. 450 nm, and some compounds exhibited strong fluorescence at ca. 530 nm with excellent quantum yields in ethyl acetate solution. DNA binding properties of these pyridophenazines to calf thymus DNA (CT DNA) were studied in phosphate buffered saline at pH 7.4 by means of fluorescence titration. All compounds showed high binding affinity toward CT DNA with binding constant values in the range of 10~6 M~(-1), with fluorescence enhancement upon their binding to CT DNA. The fluorescent aminoethylpiperidine substituted pyridophenazine was employed as a sensitive agent for DNA determination with a limit of detection of 65 nM over a linear range of 100-1000 nM. The fluorescence titration and Topi mediated DNA unwinding assay showed that this derivative exhibited DNA intercalation.
机译:合成了一系列吡啶并吩嗪衍生物,并表征为DNA嵌入荧光团。这些吡啶并吩嗪在大约2℃处显示最大吸收。 450 nm,并且某些化合物在大约200 nm处显示强荧光。 530 nm,在乙酸乙酯溶液中具有优异的量子产率。通过荧光滴定法在pH 7.4的磷酸盐缓冲盐水中研究了这些吡啶并吩嗪与小牛胸腺DNA(CT DNA)的DNA结合特性。所有化合物均对CT DNA具有很高的结合亲和力,结合常数在10〜6 M〜(-1)范围内,与CT DNA结合后荧光增强。荧光氨基乙基哌啶取代的吡啶并吩嗪用作DNA测定的敏感剂,线性范围为100-1000 nM,检测极限为65 nM。荧光滴定法和Topi介导的DNA展开实验表明,该衍生物表现出DNA嵌入。

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