Colorimetric sensing of trace UO22+ by using nanogold-seeded nucleation amplification and label-free DNAzyme cleavage reaction
In pH 4.4 HACNaAC buffer solution at 80 C, nanogold particles (NG) strongly enhanced the slow, colored reaction of Ag( i )gallic acid to form nanosilver particles, which exhibited a strong surface plasmon resonance (SPR) absorption peak at 460 nm, but the aggregated nanogold particles (ANG) exhibite...
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Published in | Analyst (London) Vol. 137; no. 8; pp. 1866 - 1871 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
01.01.2012
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Abstract | In pH 4.4 HACNaAC buffer solution at 80 C, nanogold particles (NG) strongly enhanced the slow, colored reaction of Ag(
i
)gallic acid to form nanosilver particles, which exhibited a strong surface plasmon resonance (SPR) absorption peak at 460 nm, but the aggregated nanogold particles (ANG) exhibited a weak enhancement. The increased absorption value at 460 nm was linear to the NG concentration in the range of 3.672.5 ng mL
1
Au. In pH 5.5 MES buffer solution at 80 C, single-stranded substrate DNA and DNAzyme hybridize to form double-stranded DNA (dsDNA). The presence of uranyl (UO
2
2+
) resulted in cleavage of the substrate DNA of dsDNA, releasing a short, single-stranded DNA that can be adsorbed onto the NG and protect them from aggregation; those un-adsorbed NG were aggregated to ANG. As the UO
2
2+
concentration increased, more short, single-stranded DNA were released, and more NG were protected by the cleavage of substrate single-strand DNA, so the colored particle reaction and the absorption value at 460 nm enhanced linearly. On those grounds, 0.0830.67 nmol L
1
UO
2
2+
can be detected rapidly by this colorimetric sensing assay, with a detection limit of 0.04 nmol L
1
.
A new nanogold enhanced spectrophotometric method is proposed for the detection trace UO
2
2+
, with simplicity, rapidity, low-cost, high sensitivity and selectivity. |
---|---|
AbstractList | In pH 4.4 HACNaAC buffer solution at 80 C, nanogold particles (NG) strongly enhanced the slow, colored reaction of Ag(
i
)gallic acid to form nanosilver particles, which exhibited a strong surface plasmon resonance (SPR) absorption peak at 460 nm, but the aggregated nanogold particles (ANG) exhibited a weak enhancement. The increased absorption value at 460 nm was linear to the NG concentration in the range of 3.672.5 ng mL
1
Au. In pH 5.5 MES buffer solution at 80 C, single-stranded substrate DNA and DNAzyme hybridize to form double-stranded DNA (dsDNA). The presence of uranyl (UO
2
2+
) resulted in cleavage of the substrate DNA of dsDNA, releasing a short, single-stranded DNA that can be adsorbed onto the NG and protect them from aggregation; those un-adsorbed NG were aggregated to ANG. As the UO
2
2+
concentration increased, more short, single-stranded DNA were released, and more NG were protected by the cleavage of substrate single-strand DNA, so the colored particle reaction and the absorption value at 460 nm enhanced linearly. On those grounds, 0.0830.67 nmol L
1
UO
2
2+
can be detected rapidly by this colorimetric sensing assay, with a detection limit of 0.04 nmol L
1
.
A new nanogold enhanced spectrophotometric method is proposed for the detection trace UO
2
2+
, with simplicity, rapidity, low-cost, high sensitivity and selectivity. |
Author | Jiang, Zhiliang Liang, Aihui Xu, Lili Wen, Guiqing Wang, Lisheng Zhang, Yi Luo, Yanghe |
AuthorAffiliation | Guangxi Key Laboratory of Environmental Engineering and Protection and Assessment Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection of the Ministry of Education Guangxi Normal University |
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Keywords | Trace analysis Chemical analysis Nucleation Gallic acid Color reaction Colorimetry Single stranded DNA Concentration Buffer solution Chemical enrichment Aggregation Substrate Gene amplification Double stranded DNA Absorption Adsorption Detection limit pH Cleavage Peak Surface plasmon resonance Uranyl Silver I |
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i
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Title | Colorimetric sensing of trace UO22+ by using nanogold-seeded nucleation amplification and label-free DNAzyme cleavage reaction |
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