Abstract

Histamine is an indicator of food quality and indispensable in the efficient functioning of various physiological systems. Rapid and sensitive determination of histamine is urgently needed in food analysis and clinical diagnostics. Traditional histamine detection methods require qualified personnel, need complex operation processes, and are time-consuming. In this study, a biofunctionalized nanoporous alumina membrane based electrochemical biosensor with magnetic nanoparticles (MNPs) concentration and signal amplification was developed for histamine determination. Nanoporous alumina membranes were modified by anti-histamine antibody and integrated into polydimethylsiloxane (PDMS) chambers. The specific antibody modified MNPs were used to concentrate histamine from samples and transferred to the antibody modified nanoporous membrane. The MNPs conjugated to histamine were captured in the nanopores via specific reaction between histamine and anti-histamine antibody, resulting in a blocking effect that was amplified by MNPs in the nanopores. The blockage signals could be measured by electrochemical impedance spectroscopy across the nanoporous alumina membrane. The sensing platform had great sensitivity and the limit of detection (LOD) reached as low as 3 nM. This biosensor could be successfully applied for histamine determination in saury that was stored in frozen conditions for different hours, presenting a potentially novel, sensitive, and specific sensing system for food quality assessment and safety support.

Highlights

  • Histamine, one of the biogenic amines, is synthesized by basophils, mast cells, enterochromaffine cells, platelets, and histaminergic neurons in vivo

  • We reported the use of nanoporous alumina membranes based electrochemical biosensor with biofunctional magnetic nanoparticles (MNPs) concentration for histamine determination in seafood

  • 4 MNPs were activated by ethylcarbodiimide hydrochloride (EDC)/NHS and modified with anti-histamine antibody

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Summary

Introduction

One of the biogenic amines, is synthesized by basophils, mast cells, enterochromaffine cells, platelets, and histaminergic neurons in vivo. Histamine is formed by enzymatic decarbonylation of histidine by bacterial action with improper processing procedures or inappropriate storage conditions of food, and could be present in substantial amounts in fermented food stuffs and seafood, especially saury, mackerel, sardine, tuna, herring, and anchovy [1,2]. It is often used as one of the indicators for food quality control. Rapid and sensitive determination of histamine is urgently needed in clinical and food analysis

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