Literature DB >> 19855371

ELIME (enzyme linked immuno magnetic electrochemical) method for mycotoxin detection.

Daniela Romanazzo1, Francesco Ricci, Silvia Vesco, Silvia Piermarini, Giulia Volpe, Danila Moscone, Giuseppe Palleschi.   

Abstract

Immunoassays are a valid alternative to the more expensive and time consuming quantitative HPLC or GC(1, 2) methods for the screening detection of hazardous mycotoxins in food commodities. In this protocol we show how to fabricate and interrogate an electrochemical competitive Enzyme linked immunomagnetic assay based on the use of magnetic beads as solid support for the immunochemical chain(3) and screen printed electrodes as sensing platform. Our method aims to determine the total amount of HT-2 and T-2 toxins, mycotoxins belonging to the trichothecenes family and of great concern for human health(4). The use of an antibody clone with a cross reactivity of 100% towards HT-2 and T-2 allows to simultaneously detect both toxins with similar sensitivity(5). The first step of our assay is the coating step where we immobilize HT2-KLH conjugate toxin on the surface of magnetic beads. After a blocking step, necessary to avoid non-specific absorptions, the addition of a monoclonal antibody allows the competition between immobilized HT-2 and free HT-2 or T-2 present in the sample or dissolved in a standard solution. At the end of the competition step, the amount of monoclonal antibody linked to the immobilized HT-2 will be inversely proportional to the amount of toxin in the sample solution. A secondary antibody labeled with alkaline phosphatase (AP) is used to reveal the binding between the specific antibody and the immobilized HT-2. The final measurement step is performed by dropping an aliquot of magnetic bead suspension, corresponding to a specific sample/standard solution, on the surface of a screen-printed working electrode; magnetic beads are immobilized and concentrated by means of a magnet placed precisely under the screen-printed electrode. After two minutes of incubation between magnetic beads and a substrate for AP, the enzymatic product is detected by Differential Pulse Voltammetry (DPV) using a portable instrument (PalmSens) also able to initiate automatically eight measurements within an interval of few seconds.

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Year:  2009        PMID: 19855371      PMCID: PMC3164056          DOI: 10.3791/1588

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  5 in total

Review 1.  A review on novel developments and applications of immunosensors in food analysis.

Authors:  Francesco Ricci; Giulia Volpe; Laura Micheli; Giuseppe Palleschi
Journal:  Anal Chim Acta       Date:  2007-11-04       Impact factor: 6.558

2.  Appropriate calibration curve fitting in ligand binding assays.

Authors:  John W A Findlay; Robert F Dillard
Journal:  AAPS J       Date:  2007-06-29       Impact factor: 4.009

3.  Force differentiation in recognition of cross-reactive antigens by magnetic beads.

Authors:  Tamara Y Morozova; Victor N Morozov
Journal:  Anal Biochem       Date:  2007-12-08       Impact factor: 3.365

Review 4.  The state-of-the-art in the analysis of type-A and -B trichothecene mycotoxins in cereals.

Authors:  R Krska; S Baumgartner; R Josephs
Journal:  Fresenius J Anal Chem       Date:  2001-10

Review 5.  State of the art of trichothecenes analysis.

Authors:  Priska Koch
Journal:  Toxicol Lett       Date:  2004-10-10       Impact factor: 4.372

  5 in total
  1 in total

1.  Studies in the use of magnetic microspheres for immunoaffinity extraction of paralytic shellfish poisoning toxins from shellfish.

Authors:  Raymond Devlin; Katrina Campbell; Kentaro Kawatsu; Christopher Elliott
Journal:  Toxins (Basel)       Date:  2011-01-04       Impact factor: 4.546

  1 in total

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