检出限
生物结合
免疫分析
毒品检测
胶体金
生物传感器
拉曼散射
纳米技术
材料科学
色谱法
拉曼光谱
化学
纳米颗粒
生物
免疫学
光学
抗体
物理
作者
Jian Tu,Ting Wu,Qing Yu,Jiaxuan Li,Shuai Zheng,Kezong Qi,Guohui Sun,Rui Xiao,Chongwen Wang
标识
DOI:10.1016/j.jhazmat.2023.130912
摘要
Direct, convenient, and sensitive monitoring of the residues of multiple drugs in complex environments is important but remains a challenge. Here, we report a surface-enhanced Raman scattering (SERS)-based multiplexed lateral flow immunoassay (LFA) that supports the simultaneous and sensitive detection of commonly used drugs kanamycin, ractopamine, clenbuterol, and chloramphenicol in unprocessed complex samples through the dual signal amplification strategy of numerous efficient hotspots and magnetic enrichment. Multilayered magnetic-core dual-shell nanoparticles ([email protected]) with controllable subtle nanogaps were fabricated via the polyethyleneimine-mediated layer-by-layer (LBL) assembly of two layers of [email protected] satellites onto superparamagnetic Fe3O4 cores and conjugated with specific antibodies as multifunctional tags in the LFA system for rapid capture, separation, and quantitative analysis. Two Raman reporters were embedded in internal nanogaps and modified on the surface of [email protected] for the simultaneous and ultrasensitive detection of four targets on two test lines, which greatly simplified the fabrication and signal reading of SERS-LFA. The proposed assay can rapidly detect multiple drug residues in 35 min with detection limits down to pg/mL level. Moreover, the [email protected]–based SERS-LFA demonstrated better stability, higher throughput, and superior sensitivity (at least 400 times) than traditional colloidal gold immunochromatography, showing its great potential in the field of point-of-care testing.
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