ZnO nanoflower-based photoelectrochemical DNAzyme sensor for the detection of Pb2+
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
24508815
DOI
10.1016/j.bios.2014.01.026
PII: S0956-5663(14)00029-3
Knihovny.cz E-zdroje
- Klíčová slova
- DNAzyme, Lead contamination, Photoelectrochemical sensor, ZnO nanoflower,
- MeSH
- biosenzitivní techniky přístrojové vybavení MeSH
- chemické látky znečišťující vodu analýza MeSH
- design vybavení MeSH
- DNA katalytická chemie MeSH
- elektrochemické techniky přístrojové vybavení MeSH
- interkalátory chemie MeSH
- jezera analýza MeSH
- limita detekce MeSH
- nanostruktury chemie ultrastruktura MeSH
- olovo analýza MeSH
- oxid zinečnatý chemie MeSH
- pitná voda analýza MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chemické látky znečišťující vodu MeSH
- DNA katalytická MeSH
- interkalátory MeSH
- olovo MeSH
- oxid zinečnatý MeSH
- pitná voda 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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