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基于离心微流控芯片的实时荧光环介导等温扩增技术对高价值牛奶的多重确证。

Multiple authentications of high-value milk by centrifugal microfluidic chip-based real-time fluorescent LAMP.

机构信息

Institute of Quality Standard & Testing Technology for Agro-Products, Key Laboratory of Agro-product Quality and Safety, Chinese Academy of Agricultural Sciences, Beijing 100081, People's Republic of China.

Willingmed Corporation, 156 Jinghai Industrial Parkway, Daxing District, Beijing 100176, People's Republic of China; CapitalBio Corporation, 18 Life Science Parkway, Changping District, Beijing 102206, People's Republic of China.

出版信息

Food Chem. 2021 Jul 30;351:129348. doi: 10.1016/j.foodchem.2021.129348. Epub 2021 Feb 20.

Abstract

Adulteration of food ingredients, particularly replacement of high-value milk with low-cost milk, affects food safety. For rapid and accurate identification of the possible adulterating milk species in an unknown sample, a centrifugal microfluidic chip-based real-time fluorescent multiplex loop-mediated isothermal amplification (LAMP) assay was developed to simultaneously detect milk from cow, camel, horse, goat, and yak. Using precoated primers in different reaction wells, the centrifugal microfluidic chip markedly simplified the detection process and reduced false-positive results. The entire amplification was completed within 90 min with a genomic detection limit of 0.05 ng/µL in cow, camel, horse, and goat milk and 0.005 ng/µL in yak milk. Using simulated adulterated samples for validation, the detection limit for adulterated milk samples was 2.5%, satisfying authentication requirements, as the proportion of adulterated milk higher than 10% affects economic interests. Therefore, this simple, centrifugal, microfluidic chip-based multiplex real-time fluorescent LAMP assay can simultaneously detect common milk species in commercial products to enable accurate labeling.

摘要

食品成分的掺假,特别是用低成本的牛奶替代高价值的牛奶,会影响食品安全。为了快速准确地识别未知样品中可能存在的掺假牛奶种类,开发了一种基于离心微流控芯片的实时荧光多重环介导等温扩增(LAMP)检测方法,用于同时检测牛奶中的牛、骆驼、马、山羊和牦牛。通过在不同反应孔中预涂覆引物,离心微流控芯片显著简化了检测过程,减少了假阳性结果。整个扩增过程在 90 分钟内完成,牛、骆驼、马和山羊奶的基因组检测限为 0.05ng/µL,牦牛奶的检测限为 0.005ng/µL。使用模拟掺假样品进行验证,掺假牛奶样品的检测限为 2.5%,满足认证要求,因为掺假牛奶的比例高于 10%会影响经济利益。因此,这种简单、离心、基于微流控芯片的多重实时荧光 LAMP 检测方法可以同时检测商业产品中的常见牛奶种类,实现准确标记。

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