Published August 30, 2015 | Version v1
Journal article

DNA derived fluorescent bio-dots for sensitive detection of mercury and silver ions in aqueous solution

  • 1. University of Chinese Academy of Sciences, Beijing 100049 (China)
  • 2. Laboratory of Environmental Science and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China)
  • 3. Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education and International Center for Dielectric Research, Xi'an Jiaotong University, Xi'an 710049 (China)

Description

Highlights: • First application of a DNA derived fluorescent bio-dot for metal sensing. • Bio-dot was conveniently obtained via a mild thermal hydro-thermal synthesis. • Bio-dot was directly used for fluorescent sensing without further modification. • Bio-dot showed good fluorescent sensing property for Hg(II) and Ag(I). • Formation of T–Hg–T and C–Ag–C structures played key roles in sensing. - Abstract: Inspired by the high affinity between heavy metal ions and bio-molecules as well as the low toxicity of carbon-based quantum dots, we demonstrated the first application of a DNA derived carbonaceous quantum dots, namely bio-dots, in metal ion sensing. The present DNA-derived bio-dots contain graphitic carbon layers with 0.242 nm lattice fringes, exhibit excellent fluorescence property and can be obtained via a facile hydrothermal preparation procedure. Hg(II) and Ag(I) are prone to be captured by the bio-dots due to the existence of residual thymine (T) and cytosine (C) groups, resulting in a quenched fluorescence while other heavy metal ions would cause negligible changes on the fluorescent signals of the bio-dots. The bio-dots could be used as highly selective toxic-free biosensors, with two detecting linear ranges of 0–0.5 μM and 0.5–6 μM for Hg(II) and one linear range of 0–10 μM for Ag(I). The detection limits (at a signal-to-noise ratio of 3) were estimated to be 48 nM for Hg(II) and 0.31 μM for Ag(I), respectively. The detection of Hg(II) and Ag(I) could also be realized in the real water sample analyses, with satisfying recoveries ranging from 87% to 100%

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2015.04.143

Additional details

Identifiers

DOI
10.1016/j.apsusc.2015.04.143;
PII
S0169-4332(15)01001-6;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
347
Journal Page Range
p. 505-513
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.