PVP-coated graphene oxide for selective determination of ochratoxin A via quenching fluorescence of free aptamer

被引:216
作者
Sheng, Linfeng [1 ,2 ]
Ren, Jiangtao [1 ]
Miao, Yuqing [2 ]
Wang, Jiahai [1 ]
Wang, Erkang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Zhejiang Normal Univ, Coll Chem & Life Sci, Inst Phys Chem, Lab Biomimet Electrochem Biosensors, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene oxide; Ochratoxin A; Fungi toxin; DNA aptamer; BACTERIAL TOXINS; IMMUNOSENSOR; DIAGNOSTICS; MOLECULES; ASSAY;
D O I
10.1016/j.bios.2011.01.032
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper, we developed a simple method to detect fungi toxin (ochratoxin A) produced by Aspergillus Ochraceus and Penicillium verrucosumm, utilizing graphene oxide as quencher which can quench the fluorescence of FAM (carboxyfluorescein) attached to toxin-specific aptamer. By optimizing the experimental conditions, we obtained the detection limit of our sensing platform based on bare graphene oxide to be 1.9 mu M with a linear detection range from 2 mu M to 35 mu M. Selectivity of this sensing platform has been carefully investigated; the results showed that this sensor specifically responded to ochratoxin A without interference from other structure analogues (N-acetyl-L-phenylalanine and warfarin) and with only limited interference from ochratoxin B. Experimental data showed that ochratoxin A as well as other structure analogues could adsorb onto the graphene oxide. As compared to the non-protected graphene oxide based biosensor, PVP-protected graphene oxide reveals much lower detection limit (21.8 nM) by two orders of magnitude under the optimized ratio of graphene oxide to PVP concentration. This sensor has also been challenged by testing 1% red wine containing buffer solution spiked with a series of concentration of ochratoxin A. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3494 / 3499
页数:6
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