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Scanometric nanomolar lead (II) detection using DNA-functionalized gold nanoparticles and silver stain enhancement
被引:32
作者:
Chen, Beibei
[1
]
Wang, Zebo
[1
]
Hu, Dongxue
[1
]
Ma, Qingqing
[1
]
Huang, Linna
[1
]
Xv, Chengyin
[2
]
Guo, Zhiyong
[1
]
Jiang, Xiaohua
[3
]
机构:
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, State Key Lab Base Novel Funct Mat & Preparat Sci, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Univ, Coll Sci & Technol, Ningbo 315212, Zhejiang, Peoples R China
[3] Shenzhen Polytech, Sch Appl Chem & Biol Technol, Shenzhen 518055, Peoples R China
来源:
SENSORS AND ACTUATORS B-CHEMICAL
|
2014年
/
200卷
基金:
中国国家自然科学基金;
关键词:
Gold label silver stain (GLSS);
DNAzyme;
Gold nanoparticles;
Lead (Pb2+) detection;
FREE COLORIMETRIC DETECTION;
DNAZYME;
IONS;
CATALYSIS;
D O I:
10.1016/j.snb.2014.04.066
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Based on gold label silver stain method, a facile, sensitive and selective scanometric method for the detection of lead (II) was developed. The main components of the method include "8-17" DNAzyme functionalized gold nanoparticles (AuNPi), capture DNA functionalized gold nanoparticles (AuNP2), and silver staining. In presence of lead (II), AuNPi was cleaved into different pieces that were captured by AuNP2; and became aggregated and formed network structures. These aggregate structures hindered the exposure of gold particles during the silver staining, resulting in a reduced gray values compared with that in the absence of lead (II). Using the gray value of silver stain signals, the developed scanometric assay realized a semi-quantitative detection of nanomolar levels of lead (II), ranging from 2 to 1000 nmol/L (about 0.4-200 ppb), without significant interference from other metal ions. Results suggested that this scanometric method is a simple, sensitive, selective, and portable tool for the onsite detection of nanomolar levels of lead (II). (C) 2014 Elsevier BM. All rights reserved.
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页码:310 / 316
页数:7
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