In situ Raman enhancement strategy for highly sensitive and quantitative lateral flow assay

• Published in: Analytical and bioanalytical chemistry 2022, Vol.414 (1), p.507-513
• Main Authors: Shen, Haicong, Song, Eunyeong, Wang, Yang, Meng, Lingyan, Dong, Jing, Lin, Bingqian, Huang, Di, Guan, Zhichao, Yang, Chaoyong, Zhu, Zhi
• Format: Article
• Language: English
• Subjects: ABCs 20th Anniversary; Analytical Chemistry; Assaying; Biochemistry; Biological Assay; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Cost benefit analysis; Fluorescence; Food Science; Gold; Identification and classification; Immunoassay; Laboratory Medicine; Limit of Detection; Metal Nanoparticles; Metal surfaces; Methods; Monitoring/Environmental Analysis; Nanoparticles; Peptides; Procalcitonin; Raman effect; Raman spectra; Research Paper; Selectivity; Spectrum Analysis, Raman - methods; Stability analysis
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-021-03419-z

As a paper-based analytical platform, lateral flow assay (LFA) gets benefit from the rapid analysis, low cost, high selectivity, good stability, and user-friendliness, and thus has been widely used in rapid screening or assisted diagnosis. Nevertheless, LFA still suffers from low detection sensitivity via the naked eye, limiting its applications to qualitative and semi-quantitative tests. To enhance the signal readout, various nanoparticle signal tags have been employed to replace traditional colloidal gold nanoparticles (AuNPs), such as fluorescent nanoparticles (FNPs), magnetic nanoparticles (MNPs), and Raman reporter-labeled nanoparticles. In particular, Raman reporter-labeled nanoparticles are extremely sensitive due to remarkable signal enhancement effect on metal surface. However, the application of LFA is still hampered by the poor stability of Raman reporter-labeled nanoparticles. Herein, we developed an in situ Raman enhancement strategy to create a surface-enhanced Raman scattering (SERS) signal on the AuNPs, shortened as “i-SERS,” which not only preserves the original advantages of the colloidal gold strip (AuNPs-LFA), but also realizes highly sensitive and quantitative detection. We applied the i-SERS for procalcitonin (PCT) detection. The experimental process takes only 16 min, and the limit of detection (LOD) is 0.03 ng mL −1 , far below the value using AuNPs-LFA. These results indicate that i-SERS assay was highly sensitive and suitable for the rapid detection of PCT. Graphical abstract