Download | - View accepted manuscript: Detection of azaspiracids in mussels using electrochemical immunosensors for fast screening in monitoring programs (PDF, 5.0 MiB)
|
---|
DOI | Resolve DOI: https://doi.org/10.1016/j.snb.2018.02.046 |
---|
Author | Search for: Leonardo, Sandra; Search for: Kilcoyne, Jane; Search for: Samdal, Ingunn A.; Search for: Miles, Christopher O.1; Search for: O’sullivan, Ciara K.; Search for: Diogène, Jorge; Search for: Campàs, Mònica |
---|
Affiliation | - National Research Council of Canada. Measurement Science and Standards
|
---|
Format | Text, Article |
---|
Subject | azaspiracid; antibody; electrochemical immunosensor; protein G; biotin; mussel |
---|
Abstract | Given the widespread occurrence of azaspiracids (AZAs), it is clearly necessary to advance in simple and low-cost methods for the rapid detection of these marine toxins in order to protect seafood consumers. To address this need, electrochemical immunosensors for the detection of AZAs based on a competitive direct immunoassay using peroxidase-labelled AZA as a tracer were developed. An anti-AZA polyclonal antibody was immobilised in a controlled and stable manner on protein G or avidin-coated electrodes. Experimental conditions were first optimised using colorimetric immunoassays on microtitre plates, providing intermediate products already applicable to the accurate detection of AZAs. Then, transfer of the protein G and avidin–biotin interaction-based immunoassays to 8-electrode arrays provided compact and miniaturised devices for the high-throughput detection of AZAs. The low amounts of immunoreagents required as well as the potential for reusability of the avidin–biotin interaction-based immunosensors represented significant economic savings as well as a contribution to sustainability. The electrochemical immunosensors enabled the quantification of all regulated AZAs below the regulatory limit, as well as a broad range of other toxic AZA analogues (from 63 ± 3 to 2841 ± 247 μg AZA-1 equiv./kg for the protein G-based immunosensor and from 46 ± 2 to 3079 ± 358 μg AZA-1 equiv./kg for the avidin–biotin interaction-based immunosensor). The good agreement between the results obtained by the immunosensors and LC–MS/MS in the analysis of naturally contaminated mussel samples demonstrated the easy implementation of electrochemical immunosensors for routine analysis of AZAs in food safety monitoring programs. |
---|
Publication date | 2018-02-06 |
---|
Publisher | Elsevier |
---|
In | |
---|
Language | English |
---|
Peer reviewed | Yes |
---|
NPARC number | 23003585 |
---|
Export citation | Export as RIS |
---|
Report a correction | Report a correction (opens in a new tab) |
---|
Record identifier | 71b3d66c-81a1-4d44-bfc5-74b842e4d41e |
---|
Record created | 2018-07-20 |
---|
Record modified | 2020-06-03 |
---|