Indexed by:期刊论文
Date of Publication:2009-08-15
Journal:BIOSENSORS & BIOELECTRONICS
Included Journals:SCIE、EI、PubMed
Volume:24
Issue:12
Page Number:3442-3447
ISSN No.:0956-5663
Key Words:DNA; ctDNA; Fluorescence probe; Pyrene; Ratiometric
Abstract:Fluorescent DNA probes with 1,6-hexanediyl as the linker between two pyrenes, phenylpyrenes or phenylethynyl pyrene fluorophores were synthesized (Py-1, Py-2 and Py-3) and their interactions with DNA were studied by UV-vis absorption spectra, fluorescence spectra and viscosity measurements. The probes show red-shifted emission compared with pyrene (up to 20 nm). We found the interaction of these probes with DNA can be either intercalation or groove binding. Ratiometric fluorometry (ratio of the monomer and excimer emission intensity versus concentration of DNA) was achieved with these probes for DNA quantification (with limit of detection, LOD, up to 0.1 mu g/mL). We also found that the undesired oxygen sensitivity of the emission intensity of pyrene fluorophore can be greatly suppressed by extending the pi-conjugation framework of pyrene (the I(Ar)/I(air) value is decreased from 8.10 for pyrene to less than 2.20 for the DNA probes described herein). (C) 2009 Elsevier B.V. All rights reserved.
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Gender:Male
Alma Mater:Jilin University
Degree:Doctoral Degree
School/Department:School of Chemistry Engineering
Discipline:Organic Chemistry. Applied Chemistry. Physical Chemistry (including Chemical Physics)
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