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A novel fluorescent aptasensor based on 3D porous nitrogen-sulfur co-doped carbon mesh and hybridization chain reaction for sensitive detection of ochratoxin A.
Qiao, Mengxiang; Liu, Mingwei; Wan, Zhigang; Suo, Zhiguang; Liu, Yong; Wei, Min.
Afiliación
  • Qiao M; College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, People's Republic of China.
  • Liu M; College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, People's Republic of China.
  • Wan Z; Food Inspection and Quarantine Technology Center of Shenzhen Customs, Shenzhen, 518045, People's Republic of China.
  • Suo Z; College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, People's Republic of China.
  • Liu Y; College of Chemistry and Chemical Engineering, Henan University, Kaifeng, 475004, People's Republic of China.
  • Wei M; College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, People's Republic of China. wei_min80@163.com.
Mikrochim Acta ; 190(8): 313, 2023 07 20.
Article en En | MEDLINE | ID: mdl-37470836
ABSTRACT
A novel three-dimensional (3D) porous nitrogen-sulfur co-doped carbon (N-S-C) mesh was synthesized and used for the first time as the quenching material to construct a fluorescent aptasensor for ochratoxin A (OTA) detection. The fluorescent aptasensor with enzyme-free signal amplification strategy was developed by using cDNA as a promoter to trigger hybridization chain reaction (HCR), which effectively improved the sensitivity of this aptasensor. In the absence of OTA, 3D porous N-S-C mesh can adsorb carboxyfluorescein FAM-labeled hairpin DNA1 (H1-FAM) and hairpin DNA2 (H2) and quench the fluorescence of FAM. In the presence of the OTA, the OTA specifically binds to the aptamer strand and the DNA duplex undergoes dissociation. The released cDNA in turn serves as a promoter for HCR, and the strand assembly of H1-FAM and H2 is triggered by the promoter to generate long-strand DNA polymers via HCR, resulting in an increasing fluorescent signal. Under optimal conditions, there was a good linear relationship between lgCOTA and fluorescence intensity difference in the range 0.01-500 ng/mL (R2 = 0.993), and the detection limit was 2.7 pg/mL. The designed sensor platform was applied to determine spiked OTA in peanut, wheat flour, corn flour, black tea, and wine with recoveries in the range of 94.4-119.6%.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carbono / Aptámeros de Nucleótidos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carbono / Aptámeros de Nucleótidos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Mikrochim Acta Año: 2023 Tipo del documento: Article