Treffer: Simulation-guided optimization of one-step gold nanoparticle amplification for paper-based detection of anti-IFN-γ autoantibodies.

Title:
Simulation-guided optimization of one-step gold nanoparticle amplification for paper-based detection of anti-IFN-γ autoantibodies.
Authors:
Alizargar, Azadeh1 (AUTHOR), Alizargar, Javad1,2 (AUTHOR) 8javad@ntunhs.edu.tw
Source:
Biosensors & Bioelectronics. Feb2026, Vol. 294, pN.PAG-N.PAG. 1p.
Database:
Academic Search Index

Weitere Informationen

Adult-onset immunodeficiency (AOID) caused by anti-interferon-γ autoantibodies (anti-IFN-γ Abs) lacks rapid, sensitive diagnostic tools suitable for field use. A recent innovation—3D origami paper-based analytical devices (3D-osPADs) with gold nanoparticle amplification—offers a promising platform for single-step detection. This study uses computational modeling to validate and optimize the 3D-osPAD system, enhancing its diagnostic performance and scalability. We implemented a multi-step simulation pipeline encompassing calibration curve modeling, MES buffer-pH optimization, ROC and machine learning analysis under noise, Bayesian logistic regression for detection limits, vertical capillary flow modeling, and reagent stability estimation. All simulations were performed using open-source Python libraries in Google Colab. Simulations reproduced the 10 × sensitivity gain reported by Chien et al., reducing the detection limit from 0.01 to 0.001 μg/mL. MES-pH modeling identified an optimal amplification window at pH 5 and 150 mM MES. ROC analysis and ML classifiers (AUC >0.97) confirmed robust discrimination in noisy conditions. Bayesian modeling provided uncertainty-aware detection thresholds. Capillary flow modeling showed all six paper layers saturate in <1 s, while stability simulations highlighted the importance of cold-chain preservation for reagent integrity. Our modular in silico framework supports rapid optimization of 3D-osPAD diagnostics and provides actionable insights for low-cost, field-deployable biosensor development targeting anti-IFN-γ Abs and beyond. Our amplification occurs post-capture on immobilized Au labels and is therefore format-agnostic. We clarify how the same one-step growth can be integrated into standard lateral flow immunoassays (LFIA) without altering strip architecture or readout, thereby broadening practical applicability. • A simulation pipeline optimized a gold-amplified 3D paper-based biosensor. • Signal amplification improved sensitivity 10 × , lowering LOD to 0.001 μg/mL. • MES buffer at pH 5 and 150 mM was identified as the optimal amplification condition. • Cold-chain modeling showed >70 % signal retention at 4 °C versus rapid decay at 25 °C. • Bayesian inference and machine learning improved diagnostic performance under noise. [ABSTRACT FROM AUTHOR]