Highly sensitive trace analysis of paraquat using a surface-enhanced Raman scattering microdroplet sensor

被引:93
作者
Gao, Rongke [1 ]
Choi, Namhyun [1 ]
Chang, Soo-Ik [2 ]
Kang, Seong Ho [3 ]
Song, Joon Myong [4 ]
Cho, Seong In [5 ]
Lim, Dong Woo [1 ]
Choo, Jaebum [1 ]
机构
[1] Hanyang Univ, Dept Bionano Engn, Ansan 426791, South Korea
[2] Chungbuk Natl Univ, Dept Biochem, Cheongju 361763, South Korea
[3] Kyung Hee Univ, Dept Appl Chem, Yongin 446701, South Korea
[4] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[5] Seoul Natl Univ, Dept Biosyst & Biomat Sci & Engn, Seoul 151921, South Korea
基金
新加坡国家研究基金会;
关键词
Microdroplet sensor; Paraquat; Surface-enhanced Raman scattering; Lab on a chip; Trace analysis; SILVER; CHIP; OLIGONUCLEOTIDES; NANOPARTICLES; ADSORPTION; SUBSTRATE; SERRS; WATER;
D O I
10.1016/j.aca.2010.09.036
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report a rapid and highly sensitive trace analysis of paraquat (PQ) in water using a surface-enhanced Raman scattering (SERS)-based microdroplet sensor. Aqueous samples of PQ silver nanoparticles, and NaCl as the aggregation agent were introduced into a microfluidic channel and were encapsulated by a continuous oil phase to form a microdroplet. PQ molecules were adsorbed onto particle surfaces in isolated droplets by passing through the winding part of the channel. Memory effects, caused by the precipitation of nanoparticle aggregates on channel walls, were removed because the aqueous droplets were completely isolated by a continuous oil phase. The limit of detection CLOD) of PQ in water, determined by the SERS-based microdroplet sensor, was estimated to be below 2 x 10(-9) M, and this low detection limit was enhanced by one to two orders of magnitude compared to conventional analytical methods. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 91
页数:5
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