Pablo Llano-Suárez, Adrián Sánchez-Visedo, Inmaculada Ortiz-Gómez, María Teresa Fernández-Argüelles, Marta Prado, José Manuel Costa-Fernández, Ana Soldado
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引用次数: 0
摘要
食品安全控制是食品和农业行业的一个关键问题。为此,开发微型分析方法对于快速灵敏地检测食品添加剂、过敏原和污染物至关重要。在此,我们开发了一种基于 DNA 功能化金纳米粒子(AuNPs)和比色检测的新型生物分析方法,以芝麻种子 DNA 为目标,检测食品样品中是否含有芝麻(一种主要过敏原)。芝麻 DNA 的存在会诱导受控纳米粒子的聚集/解聚,导致颜色变化(从蓝色到红色)与芝麻 DNA 的浓度成正比。在这一策略中加入了多组分核酸酶(MNAzymes),执行等温信号放大策略,以提高检测灵敏度。此外,还使用了开源的颜色分析软件,以确保无偏见的视觉颜色变化检测,从而提高了检测的准确性和灵敏度,为进行简单、分散的分析物检测提供了可能。该方法成功地检测出了芝麻、芝麻油、橄榄油和葵花籽油中芝麻 DNA 的存在。简而言之,所开发的方法是对食品中 DNA 进行高灵敏度检测的一种简单而经济的替代方法,无需复杂的方法或昂贵的仪器。
Sesame Detection in Food Using DNA-Functionalized Gold Nanoparticles: A Sensitive, Rapid, and Cost-Effective Colorimetric Approach
Food safety control is a key issue in the food and agriculture industries. For such purposes, developing miniaturized analytical methods is critical for enabling the rapid and sensitive detection of food supplements, allergens, and pollutants. Here, a novel bioanalytical methodology based on DNA-functionalized gold nanoparticles (AuNPs) and colorimetric detection was developed to detect the presence of sesame (a major allergen) through sesame seed DNA as a target, in food samples. The presence of sesame DNA induces controlled nanoparticle aggregation/desegregation, resulting in a color change (from blue to red) proportional to sesame DNA concentration. The incorporation of multicomponent nucleic acid enzymes (MNAzymes) in this strategy has been carried out to perform an isothermal signal amplification strategy to improve the sensitivity of detection. Also, open-source software for color analysis was used to ensure an unbiased visual color-change detection, enhancing detection accuracy and sensitivity and opening the possibility of performing a simple and decentralized analyte detection. The method successfully detected the presence of sesame DNA in sesame seed, sesame oil, olive oil, and sunflower oil. In brief, the developed approach constitutes a simple and affordable alternative to perform a highly sensitive detection of DNA in food without complex methodologies or the requirement of expensive instrumentation.