Enzyme-Linked Aptamer Assays (ELAAs), based on a competition format for a rapid and sensitive detection of Ochratoxin A in wine

被引:132
作者
Barthelmebs, Lise [1 ]
Jonca, Justyna [2 ]
Hayat, Akhtar [1 ]
Prieto-Simon, Beatriz [3 ]
Marty, Jean-Louis [1 ]
机构
[1] Univ Perpignan, IMAGES, EA 4218, F-66860 Perpignan, France
[2] LEGOS, UMR 5503, F-31401 Toulouse 9, France
[3] Inst Bioengn Catalonia IBEC, Nanobioengn Grp, Barcelona 08028, Spain
关键词
Ochratoxin A; DNA aptamer; SELEX; Competitive Enzyme-Linked Aptamer Assay (ELAA); Wine analysis; DNA APTAMERS; ELECTROCHEMICAL IMMUNOSENSOR; FOOD ANALYSIS; SELECTION; MOLECULES; LIGANDS; RNA; DIAGNOSTICS; ANTIBODIES;
D O I
10.1016/j.foodcont.2010.11.005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Ochratoxin A (OTA) is one of the most important mycotoxins because of its high toxicity to both humans and animals and its occurrence in a number of basic foods and agro-products. The need to develop high-performing methods for OTA analysis able to improve the traditional ones is evident. In this work, through in vitro SELEX (Systematic Evolution of Ligands by EXponential enrichment) two aptamers, designated H8 and H12 were produced that bind with nanomolar affinity with Ochratoxin A (OTA). Two strategies were investigated by using an indirect and a direct competitive Enzyme-Linked Aptamer Assay (ELAA) and were compared to the classical competitive Enzyme-Linked Immunosorbent Assay (ELISA) for the determination of OTA in spiked red wine samples. The limit of detection attained (1 ng/mL), the midpoint value obtained (5 ng/mL) and the analysis time needed (125 min) for the real sample analysis validate the direct competitive ELAA as useful screening tool for routine use in the control of OTA level in wine. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:737 / 743
页数:7
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