Early diagnosis and monitoring of SARS-CoV-2 virus is essential to control COVID-19 outbreak. In this study, we propose a promising surface enhanced Raman scattering (SERS)-based COVID-19 biosensor for ultrasensitive detection of SARS-CoV-2 virus in untreated saliva. The SERS-immune substrate was fabricated by a novel oil/water/oil (O/W/O) three-phase liquid-liquid interfaces self-assembly method, forming two layers of dense and uniform gold nanoparticle films to ensure the reproducibility and sensitivity of SERS immunoassay. The detection was performed by an immunoreaction between the SARS-CoV-2 spike antibody modified SERS-immune substrate, spike antigen protein and Raman reporter-labeled immuno-Ag nanoparticles. This SERS-based biosensor was able to detect the SARS-CoV-2 spike protein at concentrations of 0.77 fg mL
-1
in phosphate-buffered saline and 6.07 fg mL
-1
in untreated saliva. The designed SERS-based biosensor exhibited excellent specificity and sensitivity for SARS-CoV-2 virus without any sample pretreatment, providing a potential choice for the early diagnosis of COVID-19.
A cost-effective
and highly reproducible capillary-based surface-enhanced
Raman scattering (SERS) platform for sensitive, portable detection
and identification of fentanyl is presented. Through encapsulating
gold trisoctahedra (Au TOH) in the capillary tube for the first time,
the SERS platform was constructed by combining the superior SERS properties
of Au TOH and the advantages of capillaries in SERS signal amplification,
facile sample extraction, and portable trace analysis. The effects
of the size and density of Au TOH on the SERS performance were investigated
by experiments and simulations, which showed that the maximum SERS
enhancement was obtained for Au TOH with the size of 75 nm when particle
density reached 74.54 counts/μm2. The proposed SERS
platform possesses good reproducibility with a relative standard deviation
(RSD) of less than 5%. As a demonstration, the platform was applied
to detect fentanyl spiked in aqueous solution and serum samples with
a limit of detection (LOD) as low as 1.86 and 40.63 ng/mL, respectively.
We also validated the feasibility of the designed platform for accurate
identification of trace fentanyl adulterated in heroin at mass concentration
down to 0.1% (10 ng in 10 μg total). Overall, this work advances
more explorations on capillary-based SERS platform to benefit portable
trace analysis.
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