ZnO nanoflower-based photoelectrochemical DNAzyme sensor for the detection of Pb2+
Language English Country England, Great Britain Media print-electronic
Document type Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
24508815
DOI
10.1016/j.bios.2014.01.026
PII: S0956-5663(14)00029-3
Knihovny.cz E-resources
- Keywords
- DNAzyme, Lead contamination, Photoelectrochemical sensor, ZnO nanoflower,
- MeSH
- Biosensing Techniques instrumentation MeSH
- Water Pollutants, Chemical analysis MeSH
- Equipment Design MeSH
- DNA, Catalytic chemistry MeSH
- Electrochemical Techniques instrumentation MeSH
- Intercalating Agents chemistry MeSH
- Lakes analysis MeSH
- Limit of Detection MeSH
- Nanostructures chemistry ultrastructure MeSH
- Lead analysis MeSH
- Zinc Oxide chemistry MeSH
- Drinking Water analysis MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Water Pollutants, Chemical MeSH
- DNA, Catalytic MeSH
- Intercalating Agents MeSH
- Lead MeSH
- Zinc Oxide MeSH
- Drinking Water MeSH
Lead contamination is now widespread, and exposure to lead may cause adverse effects on human beings. In this study, a photoelectrochemical sensor based on flower-like ZnO nanostructures was developed for Pb(2+) detection, using a Pb(2+)-dependent DNAzyme as the recognition unit and a double-strand DNA intercalator, Ru(bpy)2(dppz)(2+) (bpy=2,2'-bipyridine, dppz=dipyrido[3,2-a:2',3'-c] phenazine) as the photoelectrochemical signal reporter. The ZnO nanoflower was fabricated on an indium tin oxide (ITO) electrode by the convenient hydrothermal decomposition method. The morphology and photoelectrochemical property of the ZnO nanoflowers were characterized by SEM, XRD and photocurrent measurements. DNAzyme-substrate duplex was assembled on an ITO/ZnO electrode through electrostatic adsorption. In the presence of Pb(2+), RNA-cleavage activity of the DNAzyme was activated and its substrate strand was cleaved, resulting in the release of Ru(bpy)2(dppz)(2+) from the DNA film and the concomitant photocurrent decrease. The detection principle was verified by fluorescence measurements. Under the optimized conditions, a linear relationship between photocurrent and Pb(2+) concentration was obtained over the range of 0.5-20 nM, with a detection limit of 0.1 nM. Interference from other common metal ions was found negligible. Applicability of the sensor was demonstrated by analyzing lead level in human serum and Pb(2+) spiked water samples. This facile and economical sensor system showed high sensitivity and selectivity, thus can be potentially applied for on-site monitoring of lead contaminant.
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