Graphene oxide wrapped Fe3O4@Au nanostructures as substrates for aptamer-based detection of Vibrio parahaemolyticus by surface-enhanced Raman spectroscopy

被引:62
作者
Duan, Nuo [1 ]
Shen, Mofei [1 ]
Wu, Shijia [1 ,2 ]
Zhao, Changxin [1 ]
Ma, Xiaoyuan [1 ]
Wang, Zhouping [1 ,3 ]
机构
[1] Jiangnan Univ, Synerget Innovat Ctr Food Safety & Nutr, Sch Food Sci & Technol, State Key Lab Food Sci & Technol, Wuxi 214122, Peoples R China
[2] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Peoples R China
[3] Dalian Polytech Univ, Natl Engn Res Ctr Seafood, Sch Food Sci & Technol, Dalian 116034, Peoples R China
基金
中国博士后科学基金;
关键词
Pathogenic bacteria; Magnetic separation; Gold nanoparticles; Salmon; Food safety; SALMONELLA-TYPHIMURIUM; SERS; NANOPARTICLES; APTASENSOR; SELECTION;
D O I
10.1007/s00604-017-2298-9
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The authors describe a sensitive surface-enhanced Raman scattering (SERS)-based aptasensor for the detection of the food pathogen Vibrio parahaemolyticus. Nanostructures consisting of Fe3O4@ Au particles wrapped with graphene oxide (GO) were used both as SERS substrates and separation tools. A first aptamer (apt 1) was immobilized on the Fe3O4@ Au/GOnanostructures to act as a capture probe via the affinity binding of aptamer and V. parahaemolyticus. A second aptamer (apt-2) was modified with the Raman reporter molecule TAMRA to act as a SERS sensing probes that binds to the target the same way as the Fe3O4@ Au/GO-apt 1. The sandwich formed between Fe3O4@ Au/GO-apt 1/V. parahaemolyticus and apt 2-TAMRA can be separated with the aid of a magnet. The concentration of V. parahaemolyticus can be quantified by measurement of the SERS intensity of TAMRA. Under optimal conditions, the signal is linearly related to the V. parahaemolyticus concentration in the range between 1.4 x 10(2) to 1.4 x 10(6) cfu.mL(-1), with a detection limit of 14 cfu.mL(-1). Recoveries ranging from 98.5% to 105% are found when analyzing spiked salmon samples. In our perception, the assay described here is a useful tool for quantitation of V. parahaemolyticus in real samples.
引用
收藏
页码:2653 / 2660
页数:8
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