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Disposable amperometric biotool for peanut detection in processed foods by targeting a chloroplast DNA marker.
Gamella, Maria; Ballesteros, María Isabel; Ruiz-Valdepeñas Montiel, Víctor; Sánchiz, Africa; Cuadrado, Carmen; Pingarrón, José M; Linacero, Rosario; Campuzano, Susana.
Afiliación
  • Gamella M; Departamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, 28040, Madrid, Spain.
  • Ballesteros MI; Departamento de Genética, Fisiología y Microbiología, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, 28040, Madrid, Spain.
  • Ruiz-Valdepeñas Montiel V; Departamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, 28040, Madrid, Spain.
  • Sánchiz A; Departamento de Tecnología de los Alimentos, CSIC-INIA, 28040, Madrid, Spain.
  • Cuadrado C; Departamento de Tecnología de los Alimentos, CSIC-INIA, 28040, Madrid, Spain.
  • Pingarrón JM; Departamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, 28040, Madrid, Spain.
  • Linacero R; Departamento de Genética, Fisiología y Microbiología, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, 28040, Madrid, Spain. Electronic address: charolin@ucm.es.
  • Campuzano S; Departamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, 28040, Madrid, Spain. Electronic address: susanacr@quim.ucm.es.
Talanta ; 277: 126350, 2024 Sep 01.
Article en En | MEDLINE | ID: mdl-38843772
ABSTRACT
This work reports the development and application of a disposable amperometric sensor built on magnetic microcarriers coupled to an Express PCR strategy to amplify a specific DNA fragment of the chloroplast trnH-psbA. The procedure involves the selective capture of a 68-mer synthetic target DNA (or unmodified PCR products) through sandwich hybridization with RNA capture probe-modified streptavidin MBs and RNA signaling probes, labeled using antibodies specific to the heteroduplexes and secondary antibodies tagged with horseradish peroxidase. Amperometric measurements were performed on screen-printed electrodes using the H2O2/hydroquinone system. Achieving a LOD of 3 pM for the synthetic target, it was possible to detect 2.5 pg of peanut DNA and around 10 mg kg-1 of peanut in binary mixtures (defatted peanut flours prepared in spelt wheat). However, the detectability decreased between 10 and 1000 times in processed samples depending on the treatment. The Express PCR-bioplatform was applied to the detection of peanut traces in foodstuff.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arachis Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arachis Idioma: En Año: 2024 Tipo del documento: Article