适体
磁镊
镊子
检出限
化学
荧光
磁性纳米粒子
DNA
磁选
恩诺沙星
纳米颗粒
色谱法
纳米技术
材料科学
生物化学
分子生物学
生物
光学
冶金
抗生素
环丙沙星
物理化学
物理
作者
Zixuan Shang,Pengfei Ma,Imran Mahmood Khan,Yin Zhang,Zhouping Wang
出处
期刊:Food Control
[Elsevier BV]
日期:2022-10-13
卷期号:145: 109437-109437
被引量:18
标识
DOI:10.1016/j.foodcont.2022.109437
摘要
A DNA tweezers fluorescence aptasensor based on split aptamer assisted-magnetic nanoparticles (MNPs) and magnetic separation was established for the detection of Enrofloxacin (ENR). The DNA tweezers' fluorescence aptasensor consists of two arms with fluorophores (FAM) and quenchers (BHQ1) connected at both ends. Meanwhile, the high fluorescence signal can be generated with FAM and BHQ1 being spatially separated. Split aptamer 1 (SPA1) of ENR was annealed and incubated with avidin-coated MNPs. ENR and split aptamer 2 (SPA2) were added to form a sandwich structure with two split aptamer strands (MNPS-SPA1/ENR/SPA2). After magnetic separation, the supernatant did not interact with DNA tweezers, which made DNA tweezers a “turn-on” aptasensor to enhance the fluorescence signal. In the absence of ENR, SPA2 was free in the supernatant to dramatically quench the fluorescence which made DNA tweezers a “turn-off” aptasensor. The linear range of ENR detection was 0.01–100 ng/mL with a limit of detection of 0.008 ng/mL. The prepared DNA tweezers fluorescence aptasensors were applied to detect ENR in spiked milk samples, which showed good recoveries between 90.27% and 106.62%. In addition, the present method showed great potential for the target, employing a split aptamer detection platform in practical application.
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