Design of novel hybrid probe based on double recognition of aptamer-molecularly imprinted polymer-gold nanoparticles for food allergen gliadin sensing.

IF 6.1 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-12-01 Epub Date: 2025-05-28 DOI:10.1016/j.talanta.2025.128344
Selenay Sadak, Gözde Aydoğdu Tığ, Bengi Uslu
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引用次数: 0

Abstract

Gliadins are allergenic proteins that can pose various risks to human health and are found in high amounts in the most commonly consumed foods. Gliadin, a component of gluten, triggers oxidative stress in celiac disease. Using sensitive analytical methods, especially in foods containing high amounts of these proteins, is crucial for food safety. Aptamer-based biosensors are widely preferred in electroanalytical methods. One of the promising approaches regarding biosensors is the studies in which aptamer-based sensors are combined with molecularly imprinted polymers. The antibody-like binding and ability of MIP to distinguish between molecules increases the method's selectivity. Using a platform modified with aptamer and molecularly imprinted polymer hybrid (MIP) as a new synthetic receptor film, this study presents a selective and sensitive label-free aptasensor for detecting a food allergy gliadin. For this purpose, screen printed gold electrode was used. The electrode surface was electrochemically coated with gold nanoparticles to bind the aptamer to the surface; then the aptamer-gliadin complex was dripped onto the surface and adhered to it, then, o-phenylene diamine monomer was used to synthesize a MIP surface. Gliadin was determined by using differential pulse voltammetry (DPV) in a wide range from 0.25 fg/mL to 1000 pg/mL. The developed method calculated LOD for gliadin determination as 0.011 fg/mL and LOQ as 0.034 fg/mL. The devised aptasensor was not only capable to the discrimination of the commonly found allergen compounds such as bovine serum albumin (BSA), casein, and ara-H1, but also it could detect the gliadin in spiked real samples such as gluten-free bread, crackers, cookies and brown rice cakes samples in the high recovery range of 98.1-104.6 %. The method could be a promising candidate for the sensitive determination of several allergens in food sample analysis.

基于适配体-分子印迹聚合物-金纳米颗粒双重识别的新型混合探针设计用于食物过敏原麦胶蛋白检测。
麦胶蛋白是一种致敏蛋白,可能对人体健康构成各种风险,在最常食用的食物中含量很高。麦胶蛋白是谷蛋白的一种成分,会引发乳糜泻的氧化应激。使用敏感的分析方法,特别是在含有大量这些蛋白质的食品中,对食品安全至关重要。基于适配体的生物传感器在电分析方法中得到了广泛的应用。生物传感器的一个很有前途的方法是研究基于适体的传感器与分子印迹聚合物的结合。抗体样结合和MIP区分分子的能力增加了该方法的选择性。本研究以适配体和分子印迹聚合物复合物(MIP)作为新型合成受体膜,制备了一种选择性灵敏的无标记食物过敏麦胶蛋白适配体传感器。为此,采用丝网印刷金电极。在电极表面电化学涂覆金纳米颗粒,使适配体与电极表面结合;然后滴入适体-麦胶蛋白配合物并粘附于其表面,然后用邻苯二胺单体合成MIP表面。采用差分脉冲伏安法(DPV)在0.25 fg/mL ~ 1000 pg/mL范围内测定麦胶蛋白。本方法测定麦胶蛋白的定量限为0.011 fg/mL,定量限为0.034 fg/mL。该传感器不仅能对牛血清白蛋白(BSA)、酪蛋白、ara-H1等常见过敏原化合物进行鉴别,还能对无麸质面包、饼干、饼干、糙米糕等实际样品中的麦胶蛋白进行检测,回收率为98.1 ~ 104.6%。该方法可用于食品样品分析中几种过敏原的灵敏测定。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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