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基于血糖仪的生物传感器,用于使用滚环扩增法测定动物源性食品中的莱克多巴胺。

Glucometer-based biosensor for the determination of ractopamine in animal-derived foods using rolling circle amplification.

机构信息

Institute of Food & Nutrition Science and Technology, Shandong Provincial Key Laboratory of Agro-Products Processing Technology, Key Laboratory of Novel Food Resources Processing, Ministry of Agriculture, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.

School of Life Sciences and Food Engineering, Hebei University of Engineering, Handan, 056038, China.

出版信息

Mikrochim Acta. 2023 Mar 8;190(4):121. doi: 10.1007/s00604-023-05715-0.

Abstract

Screening for persistent organic pollutants (POPs) in food is a complex and challenging process, as POPs can be present in very low levels and can be difficult to detect. Herein, we developed an ultrasensitive biosensor based on a rolling circle amplification (RCA) platform using a glucometer to determine POP. The biosensor was constructed using gold nanoparticle probes modified with antibodies and dozens of primers, magnetic microparticle probes conjugated with haptens, and targets. After competition, RCA reactions are triggered, numerous RCA products hybridize with the ssDNA-invertase, and the target is successfully transformed into glucose. Using ractopamine as a model analyte, this strategy obtained a linear detection range of 0.038-5.00 ng mL and a detection limit of 0.0158 ng mL, which was preliminarily verified by screening in real samples. Compared with conventional immunoassays, this biosensor utilizes the high efficiency of RCA and the portable properties of a glucometer, which effectively improves the sensitivity and simplifies the procedures using magnetic separation technology. Moreover, it has been successfully applied to ractopamine determination in animal-derived foods, revealing its potential as a promising tool for POP screening.

摘要

食品中持久性有机污染物(POPs)的筛选是一个复杂且具有挑战性的过程,因为 POPs 可能存在于非常低的水平,并且难以检测。在此,我们开发了一种基于滚环扩增(RCA)平台的超灵敏生物传感器,使用血糖仪来测定 POP。该生物传感器是使用抗体和数十个引物修饰的金纳米颗粒探针、与半抗原偶联的磁性微粒探针以及靶标构建而成的。经过竞争后,引发 RCA 反应,大量的 RCA 产物与 ssDNA-转化酶杂交,目标物成功转化为葡萄糖。以莱克多巴胺为模型分析物,该策略获得了 0.038-5.00 ng mL 的线性检测范围和 0.0158 ng mL 的检测限,并通过对实际样品的筛选进行了初步验证。与传统免疫测定法相比,该生物传感器利用了 RCA 的高效率和血糖仪的便携性,有效地提高了灵敏度,并通过磁分离技术简化了步骤。此外,它已成功应用于动物源性食品中莱克多巴胺的测定,显示出其作为 POP 筛选的有前途工具的潜力。

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