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Preparation and application of aptamer-functionalized sorbent for the analysis of ultra-trace aflatoxin M1 and analogues in milk
•Preparation of aflatoxin M1-aptamer modified microspheres as SPE sorbents for simultaneous determination aflatoxin M1 and analogues in milk.•Functional and extraction conditions were optimized by single-factor experiments.•M1-aptamer microspheres were used to enrich and purify ultra-trace AFM1 in d...
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Published in: | Microchemical journal 2021-07, Vol.166, p.106179, Article 106179 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Preparation of aflatoxin M1-aptamer modified microspheres as SPE sorbents for simultaneous determination aflatoxin M1 and analogues in milk.•Functional and extraction conditions were optimized by single-factor experiments.•M1-aptamer microspheres were used to enrich and purify ultra-trace AFM1 in dairy products exhibited a specific and strong adsorption capacity.•A method for the determination AFM1 with low matrix effect, good sensitivity and reproducible was developed.
A novel, efficient and specific aptamer-functionalized sorbent was successfully synthesized and applied in the analysis of ultra-trace aflatoxin M1 (AFM1) and its analogues in milk. By using a gold nanoparticle-based colorimetric analysis tool, we could determine that the AFM1-aptamer (M1-aptamer) recognized and bound AFM1 to generate an aptamer-target complex. After analysis and verification, the M1-aptamer on the surface of the carboxyl microspheres were completely modified via EDC/NHs amide formation. The effects of extraction pH, extraction buffer, concentration of Mg2+ and elution solvents were investigated by single-factor experiments to determine the most suitable analysis conditions. Using these conditions, the extraction performance of the M1-aptamer-functionalized sorbent could be studied and an analytical method for AFM1 and its analogues in milk could be established. The results of adsorption equilibrium as well as adsorption selectivity experiments indicated that the M1-aptamer offered a specific adsorption site to selectively adsorb aflatoxins exhibiting a dihydrofuran oxaphthalene scaffold. The adsorption capacity of the aptamer-functionalized sorbent was 233.1 μg/g. A studied method for the determination AFM1 in milk with low matrix effect demonstrated a good linear correlation in the range of 0 to 2.0 μg/L (R2 = 0.9982) and high detection sensitivity (detection limits of 7 ng/kg in milk and 21 ng/kg in milk power). Furthermore, excellent spiked recovery and good repeatability were obtained. The method delivered specific, accurate and reproducible results for enriching and detecting ultra-trace AFM1 and its analogues in milk. |
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ISSN: | 0026-265X 1095-9149 |
DOI: | 10.1016/j.microc.2021.106179 |