Multilayer Plasmon Hybridization in Au–Ag–Au Nanoparticles Enables Extinction Amplification in Transport-Limited One-Step Confirmatory Syphilis Biosensing

表面等离子共振 胶体金 纳米颗粒 材料科学 等离子体子 免疫分析 分析物 生物结合 生物传感器 检出限 纳米技术 分析化学(期刊) 化学 等离子纳米粒子 光子学 毛细管作用 光学 微分脉冲伏安法 显微镜 光漂白
作者
Ketan Dighe,Satheesh Natarajan,Maria Iftesum,Shraddha Krishnakumar,David Skrodzki,Matthew Molinaro,Nivetha Gunaseelan,Casey N. Pinto,Manas Ranjan Gartia,Dipanjan Pan
出处
期刊:ACS Sensors [American Chemical Society]
标识
DOI:10.1021/acssensors.6c02500
摘要

Syphilis diagnosis requires pairing treponemal and non-treponemal antibody results, yet rapid tests combining both markers lose sensitivity at the low RPR titers (≤1:4) most critical in early infection and pregnancy. The limitation lies with the reporter: conventional gold nanoparticles (AuNPs) cannot generate high-contrast signals at low antibody concentrations without exceeding the diameter that allows capillary transport through a nitrocellulose membrane. Here, we report gold-silver-gold (Au-Ag-Au) multilayer plasmonic nanoparticles (ML-PNPs) that exploit interfacial plasmon hybridization to overcome this trade-off. Polyhedral 50-58 nm particles were prepared by seed-mediated growth followed by galvanic replacement, and their layered structure was confirmed by electron microscopy, elemental mapping, and X-ray photoelectron spectroscopy. A silver interlayer between chemically robust gold domains couples across two metal-dielectric interfaces, while the outer gold shell preserves colloidal stability and thiol-based bioconjugation at hydrodynamic diameters below 60 nm. Finite-difference time-domain (FDTD) simulations and hyperspectral imaging showed a broadened, red-shifted resonance (scattering maximum 658 nm vs 555 nm for AuNPs) with 18-fold enhanced absorption. In a dual-marker colorimetric lateral flow immunoassay (CLFIA), ML-PNPs improved the visual detection limit by 3-fold and required 6-fold fewer particles per visible test spot. Across 36 clinical specimens spanning RPR titers of 1:1 to 1:128, treponemal and nontreponemal test-line intensities increased by 19-46%, and low-titer 1:1 samples missed by AuNP strips were reliably detected, with full agreement with reference methods and no cross-reactivity with HIV-1 or HCV sera. Coupled with fingerstick sampling and on-strip plasma separation, this supports same-visit execution of the reverse testing algorithm in an instrument-free format.

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