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Numerical screening predicts improved sensitivity for HIV DNA detection in low-resource settings, suggesting advanced SPR technology integration.
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 2 . This impedance-matched stack (Sys 3 ) 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 −1 , a limit of detection of 2.99 × 10 −5 RIU and a quality factor of 56.9 RIU −1 , outperforming gold-based benchmarks and approaching values reported for more reactive ZnSe buffers. Reversing the dielectric sequence (Sys 4 ) increases sensitivity to 201° RIU −1 but lowers fabrication yield and storage stability, establishing Sys 3 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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Tene et al. (2025) studied this question.
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