Introduction of multilayered magnetic core-dual shell SERS tags into lateral flow immunoassay: A highly stable and sensitive method for the simultaneous detection of multiple veterinary drugs in complex samples.

J Hazard Mater

Anhui Province Engineering Laboratory for Animal Food Quality and Bio-safety, College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China; Beijing Institute of Microbiology and Epidemiology, Beijing 100850, PR China; College of Life Sciences, Anhui Agricultural University, Hefei 230036, PR China; Laboratory Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510000, PR China. Electronic address:

Published: April 2023

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 (MDAu@Ag) with controllable subtle nanogaps were fabricated via the polyethyleneimine-mediated layer-by-layer (LBL) assembly of two layers of Au@Ag satellites onto superparamagnetic FeO 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 MDAu@Ag 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 MDAu@Ag-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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http://dx.doi.org/10.1016/j.jhazmat.2023.130912DOI Listing

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