Synthesis of a new β-naphthothiazole monomethine cyanine dye for the detection of DNA in aqueous solution

被引:30
作者
El-Shishtawy, Reda M. [1 ]
Asiri, Abdullah M. [1 ]
Basaif, Salem A. [1 ]
Sobahi, T. Rashad [1 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah 21589, Saudi Arabia
关键词
Monomethine cyanine dyes; Ethidium bromide; DNA; Napthothiazole; Fluorescence enhancement; Intercalation; DOUBLE-STRANDED DNA; FLUOROMETRIC ASSAY; NUCLEIC-ACIDS; RNA; PROBES; LIGHT; STATE;
D O I
10.1016/j.saa.2010.02.026
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Novel monomethine cyanine dye (MC) derived from beta-naphthothiazole and benzothiazole has been prepared and characterized by H-1 and C-13 NMR, FTIR, ESIMS, elemental analyses, absorption and fluorescence spectroscopy. The dye was conveniently synthesized by the condensation of two sulfate heterocyclic quaternary salts. The interaction between calf thymus DNA (ct-DNA) in tris(hydroxymethyl)aminomethane-HCl (Tris-HCl) aqueous buffer solution and MC has been studied with spectral fluorescence method. The binding constant value has been determined by fluorescence titration of MC with ct-DNA concentrations. The result obtained is consistent with an intercalative binding interaction between MC and ct-DNA. Compared with ethidium bromide (EB). MC showed a huge fluorescence enhancement upon mixing with ct-DNA. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1605 / 1609
页数:5
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