College of Chemical Engineering, Zhejiang University of Technology. Hangzhou 310014, (PR China).
College of Veterinary Medicine, China Agricultural University. Beijing 100193 (PR China).
Anal Chem. 2022 Feb 15;94(6):2996-3004. doi: 10.1021/acs.analchem.1c05364. Epub 2022 Feb 2.
Antibiotics abuse has caused various problems threatening human health and ecological environment. Monitoring antibiotics residual levels is of great significance, yet still challenging for quantitative point-of-need testing with high-sensitivity and visual capability. Here we developed a competitive lateral flow immunoassay (CLFIA) platform with flexible readout for enrofloxacin (ENR), a regularly added antibiotic. To overcome the limitation of low sensitivity of traditional colloidal gold-based CLFIA, the three-dimensionally assembled gold nanoparticles (AuNPs) within dendritic silica scaffold were fabricated as signal reporters. The assembly structure effectively retained the intrinsic absorption features of hydrophobic AuNPs and greatly enhanced the light extinction ability of a single label for signal amplification. The obtained CLFIA strips can not only achieve qualitative screening of ENR at a very low concentration by naked eye (cutoff value: 0.125 ng/mL), but also enable ultrasensitive quantification of ENR by an optical scanner (limit of detection: 0.00195 ng/mL) or a smartphone (limit of detection: 0.0078 ng/mL). Moreover, to elaborate the visual inspection degree of CLFIA against traditional yes/no interpretation, a novel multirange gradient CLFIA strip was prepared for visually semiquantitative identification of ENR with four concentration ranges. The novel CLFIA platform demonstrated sensitive, specific, and reliable determination of ENR with flexible signal readout and provides a potential and invigorating pathway to point-of-need immunoassay of antibiotics.
抗生素滥用导致了威胁人类健康和生态环境的各种问题。监测抗生素残留水平具有重要意义,但对于具有高灵敏度和可视化能力的即时定量检测仍然具有挑战性。在这里,我们开发了一种具有灵活读取功能的竞争侧向流动免疫分析(CLFIA)平台,用于检测恩诺沙星(ENR)这种经常添加的抗生素。为了克服传统胶体金 CLFIA 灵敏度低的限制,我们制备了具有三维组装结构的金纳米粒子(AuNPs)作为信号报告物,其位于树枝状二氧化硅支架内。这种组装结构有效地保留了疏水性 AuNPs 的固有吸收特性,并极大地增强了单个标记的光消光能力,从而实现了信号放大。所得 CLFIA 条带不仅可以通过肉眼(检测限:0.125 ng/mL)实现对 ENR 的极低浓度的定性筛选,而且还可以通过光学扫描仪(检测限:0.00195 ng/mL)或智能手机(检测限:0.0078 ng/mL)实现对 ENR 的超灵敏定量。此外,为了详细说明 CLFIA 对传统“是/否”解释的目视检查程度,我们制备了一种新型多范围梯度 CLFIA 条带,用于对 ENR 进行目视半定量鉴定,具有四个浓度范围。新型 CLFIA 平台展示了对 ENR 的敏感、特异和可靠的检测,具有灵活的信号读取功能,为即时免疫分析抗生素提供了一种有潜力和充满活力的途径。