4.6 Article

A portable SERS reader coupled with catalytic hairpin assembly for sensitive microRNA-21 lateral flow sensing

Journal

ANALYST
Volume 146, Issue 3, Pages 848-854

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0an02177f

Keywords

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Funding

  1. National Natural Science Foundation of China [21804046, 21778020]
  2. Fundamental Research Funds for the Central Universities [2662018QD012]
  3. Natural Science Foundation of Hubei Province, China [2018CFB368]
  4. Shandong Key Laboratory of Biochemical Analysis [SKLBA1906]
  5. State Key Laboratory of Analytical Chemistry for Life Science [SKLACLS1904]

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A lateral flow microRNA-21 biosensing platform was developed using a portable SERS reader and a catalytic hairpin assembly signal amplification strategy, achieving sensitive quantification of microRNA-21 with a detection limit as low as 84 fM. This approach shows great potential for amplified point-of-care biosensing for clinical diagnosis by detecting targets in serum samples.
Nucleic acid lateral flow sensing has drawn great research attention since it has the advantages of being simple, rapid, and cost-effective. However, considering the trace amounts of the nucleic acid targets, its sensitivity is still limited. Although enormous efforts have been devoted to enhancing its sensitivity, developing a simple lateral flow sensing platform with high sensitivity remains challenging. We report a novel lateral flow microRNA-21 biosensing platform based on a portable surface enhanced Raman scattering (SERS) reader coupled with a catalytic hairpin assembly signal amplification strategy. Hairpin DNA probes were anchored on Au@Ag nanotags, and the presence of microRNA-21 triggered the formation of numerous double-stranded DNAs along with the exposure of the biotin groups. By this means, the target was recycled and signal amplification was achieved. The Au@Ag nanoprobes with exposed biotin can be captured on the test line via its interaction with streptavidin. By scanning the strip with a portable SERS reader, the sensitive quantification of microRNA-21 was realized with a detection limit as low as 84 fM. The proposed strategy was employed to detect the target in a serum sample, demonstrating its great potential in amplified point-of-care biosensing for clinical diagnosis.

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