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Updated: Jul 4, 2026

Fluorescent Lateral Flow Immunoassay Based on Quantum Dots Nanobeads
Published on: June 28, 2024
Donor-Acceptor Organic Fluorophores Encapsulated in Polystyrene Nanoparticles as High-Brightness Reporters for
Yeon Young Yoon1, Ye Jin Kim1, Ju Yeon Yu1
1Daejin University, Pocheon, Republic of Korea.
Abstract:
Fluorescent lateral flow immunoassays (LFAs) offer improved sensitivity, quantitative readout, and multiplexing over conventional colorimetric formats. However, individual organic fluorophores often provide insufficient signal for highly sensitive strip assays; although dye-loaded polymer nanoparticles can amplify fluorescence by delivering many fluorophores per particle, their performance remains limited by dye absorptivity and emissivity, self-quenching under dense loading, encapsulation efficiency, and optical background from nitrocellulose membranes. Here, we report two rationally designed donor-acceptor fluorophores, QNN and B_PEG, and encapsulate them into carboxylated polystyrene nanoparticles (PSNPs) as fluorescent reporters for C-reactive protein (CRP) LFAs. Their extended donor-acceptor structures and PEG-like side chains were designed to enhance fluorescence, reduce aggregation-related quenching, and support swelling-diffusion loading in mixed aqueous/organic media. After normalization of the commercial PS control using the PS-dominated UV absorption at 235 nm, QNN_PSNP and B_PEG_PSNP generated approximately 2- and 13-fold stronger fluorescence, respectively, than a size-comparable commercial fluorescent PS control, while preserving their optical properties after antibody conjugation and remaining photostable under continuous UV irradiation. In CRP LFAs, the QNN-based assay extended the working range to 0.1-100 ng mL⁻¹ with robust visual discrimination at the lower end, whereas the B_PEG-based assay operated over 1-100 ng mL⁻¹ as a spectrally distinct blue-emitting counterpart. The superior strip-level performance of QNN, despite its lower intrinsic quantum yield, highlights the importance of emission wavelength, optical filtering, and membrane-derived background in practical LFA sensitivity. These results identify QNN and B_PEG as complementary fluorophore candidates for PSNP-based fluorescent LFA reporters.
