Synthesis of a novel fluorescent probe based on acridine skeleton used for sensitive determination of DNA

被引:27
作者
Wu, Menghui [1 ]
Wu, Wenqiang [1 ]
Gao, Xi [1 ]
Lin, Xucong [1 ]
Xie, Zenghong [1 ]
机构
[1] Fuzhou Univ, Dept Chem, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
acridine derivative; synthesis; fluorescent quenching; DNA determination;
D O I
10.1016/j.talanta.2007.12.039
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, a novel fluorescent probe of acridine-derivitive N-((N-(2-dimethylamino)ethyl)acridine-4-carboxamide)-alpha-alanine (N-(ACR-4-CA)(alpha-ALA) was synthesized. The structure of the new compound was characterized by H-1 NMR, MS, elemental analysis, fluorescent and ultraviolet spectra. It was found that DNA had the ability to quench the fluorescence of N-(ACR-4-CA)-alpha-ALA, and the quenched intensity of fluorescence was proportional to the concentration of DNA. A method for DNA determination based on the quenching fluorescence (lambda(ex) = 260 nm, lambda(cm) = 451 nm) of N-(ACR-4-CA)-alpha-ALA was established. Under optimal conditions, the linear range is 0.05-2.0 mu g mL(-1) for both fish semen (fsDNA) and calf thymus DNA (ctDNA). The corresponding determination limits are 9.1 ng mL(-1) for fsDNA and 8.7 ng mL(-1) for ctDNA, respectively. The results suggested that the interaction mode between N-(ACR-4-CA)-alpha-ALA and DNA was intercalative binding. The intrinsic binding constant was determined and the result showed a large binding constant of N-(ACR-4-CA)-alpha-ALA with DNA. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:995 / 1001
页数:7
相关论文
共 43 条
[1]   POTENTIAL ANTITUMOR AGENTS .43. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF DIBASIC 9-AMINOACRIDINE-4-CARBOXAMIDES, A NEW CLASS OF ANTITUMOR AGENT [J].
ATWELL, GJ ;
CAIN, BF ;
BAGULEY, BC ;
FINLAY, GJ ;
DENNY, WA .
JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (11) :1481-1485
[2]   POTENTIAL ANTITUMOR AGENTS .50. INVIVO SOLID-TUMOR ACTIVITY OF DERIVATIVES OF N-[2-(DIMETHYLAMINO)ETHYL]ACRIDINE-4-CARBOXAMIDE [J].
ATWELL, GJ ;
REWCASTLE, GW ;
BAGULEY, BC ;
DENNY, WA .
JOURNAL OF MEDICINAL CHEMISTRY, 1987, 30 (04) :664-669
[3]  
Cantor C., 1980, BIOPHYSICAL CHEM, V2, P398
[4]   Ferric nanoparticle-based resonance light scattering determination of DNA at nanogram levels [J].
Cheng, Yongqiang ;
Li, Zhengping ;
Su, Yuqin ;
Fan, Yongshan .
TALANTA, 2007, 71 (04) :1757-1761
[5]   INTERACTIONS OF ACRIDINE ANTITUMOR AGENTS WITH DNA - BINDING-ENERGIES AND GROOVE PREFERENCES [J].
CRENSHAW, JM ;
GRAVES, DE ;
DENNY, WA .
BIOCHEMISTRY, 1995, 34 (41) :13682-13687
[6]  
DAVID EG, 1981, BIOCHEMISTRY-US, V20, P1887
[7]   POTENTIAL ANTITUMOR AGENTS .49. 5-SUBSTITUTED DERIVATIVES OF N-[2-(DIMETHYLAMINO)ETHYL]-9-AMINOACRIDINE-4-CARBOXAMIDE WITH INVIVO SOLID-TUMOR ACTIVITY [J].
DENNY, WA ;
ATWELL, GJ ;
REWCASTLE, GW ;
BAGULEY, BC .
JOURNAL OF MEDICINAL CHEMISTRY, 1987, 30 (04) :658-663
[8]   Fluorescence spectral study of 9-acridinecarboxylic acid and its methyl ester. Understanding the unusual fluorescence behavior of 9-anthroic acid [J].
Dey, J ;
Haynes, JL ;
Warner, IM ;
Chandra, AK .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (12) :2271-2278
[9]  
DI GC, 2005, BIOORGAN MED CHEM, V13, P5560
[10]   SPECTROSCOPIC ANALYSIS OF DRUG NUCLEIC-ACID INTERACTIONS [J].
DOUGHERTY, G ;
PIGRAM, WJ .
CRC CRITICAL REVIEWS IN BIOCHEMISTRY, 1982, 12 (02) :103-132