适体
化学
检出限
荧光
分析物
胶体金
磁选
纳米颗粒
塔克曼
磁性纳米粒子
色谱法
组合化学
纳米技术
材料科学
实时聚合酶链反应
分子生物学
生物化学
生物
基因
量子力学
物理
冶金
作者
Zewei Luo,Yimin Wang,Xiaoyong Lu,Junman Chen,Fujing Wei,Zhijun Huang,Chen Zhou,Yixiang Duan
标识
DOI:10.1016/j.aca.2017.06.037
摘要
Antibiotic abuse has been bringing serious pollution in water, which is closely related to human health. It is desirable to develop a new strategy for antibiotic detection. To address this problem, a sensitive fluorescent aptasensor for antibiotic detection was developed by utilizing gold nanoparticles modified magnetic bead composites (AuNPs/MBs) and nicking enzyme. AuNPs/MBs were synthesized with the help of polyethylenimine (PEI). The prepared AuNPs/MBs acted as dual-functional scaffolds that owned excellent magnetic separation capacity and strong covalent bio-conjugation. The non-specifically absorbed aptamers in AuNPs/MBs were less than that in MBs. Hence, the fluorescent aptasensor based on AuNPs/MBs show a better signal to background ratio than that based on carboxyl modified magnetic beads (MBs). In this work, ampicillin was employed as a model analyte. In the presence of ampicillin, the specific binding between ampicillin and aptamer induced structure-switching that led to the release of partial complementary DNA (cDNA) of aptamer. Then, the released cDNA initiated the cycle of nicking enzyme assisted signal amplification (NEASA). Therefore, a large amount of taqman probes were cleaved and fluorescence signal was amplified. The prepared fluorescent aptasensor bring sensitive detection in range of 0.1–100 ng mL−1 with the limit of detection of 0.07 ng mL−1. Furthermore, this aptasensor was also successfully applied in real sample detection with acceptable accuracy. The fluorescent aptasensor provides a promising method for efficient, rapid and sensitive antibiotic detection.
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