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Article Abstract

Surface-plasmon-resonance (SPR) sensors provide label-free nucleic-acid diagnostics, yet they must detect the sub-nanometre refractive-index changes generated by short HIV-DNA hybridisation. Using a transfer-matrix framework, we design a multilayer architecture that couples a 50 nm silver mirror to the analyte through a 7 nm (10 nm) silicon-nitride spacer capped with a monolayer of WS. This impedance-matched stack (Sys) concentrates the evanescent field at the recognition surface while chemically passivating the metal. Numerical screening calibrated with published optical constants predicts an angular sensitivity of 167° RIU, a limit of detection of 2.99 × 10 RIU and a quality factor of 56.9 RIU, outperforming gold-based benchmarks and approaching values reported for more reactive ZnSe buffers. Reversing the dielectric sequence (Sys) increases sensitivity to 201° RIU but lowers fabrication yield and storage stability, establishing Sys as the most scalable option. Proof-of-concept measurements demonstrate sub-picomolar quantification of HIV DNA in phosphate-buffered saline without enzymatic amplification. The materials palette is compatible with complementary-metal-oxide-semiconductor processes, enabling streamlined integration of high-resolution SPR sensing into point-of-care viral-load platforms for resource-limited settings.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12310735PMC
http://dx.doi.org/10.3389/fbioe.2025.1577925DOI Listing

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