Chopped optical biosensing enables temporal background subtraction for high-sensitivity fluorescence immunoassays

Fluorescence-based immunoassays are widely used for sensitive biomarker detection, but their performance at low analyte concentrations is often limited by background signals originating from unbound fluorophores, Raman scattering, and sample autofluorescence. Here, we introduce chopped optical biosensing (COB), an analytical framework that improves fluorescence immunoassay sensitivity by temporally separating background and target fluorescence. In COB, fluorophore-labeled targets captured on magnetic beads are concentrated into a small detection region using a permanent magnet. An optical chopper periodically gates the excitation beam, enabling fluorescence measurements before bead aggregation (background only) and after aggregation (target + background). Subtraction of these temporally separated signals isolates fluorescence from bead-bound targets while suppressing background contributions from unbound fluorophores, Raman scattering, and sample autofluorescence. By limiting continuous illumination, this approach also reduces photobleaching and stabilizes excitation intensity, while eliminating the need for washing steps or dynamic optical modulation. Analytical evaluation demonstrated detection limits of 61 fM for Atto 532 dye, 0.05 ng/L for interleukin-8 (IL-8), and 3 ng/mL for anti-dengue virus serotype 2 non-structural protein 1 (anti-DENV-2 NS1) immunoglobulin G (IgG), with reproducibility below 15%. The total assay time is approximately 90 min. In a targeted feasibility assessment using 64 well-characterized serum samples, the COB-based anti-DENV-2 NS1 IgG assay correctly classified all samples when compared with reference ELISA results. Combining low complexity, compact design, and energy-efficient operation with high analytical and clinical performance, COB provides a practical foundation for streamlined fluorescence immunoassay workflows and is well suited for future portable diagnostic applications.

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Publication Details

Journal
Talanta
Published
2026-03-12
DOI
https://doi.org/10.1016/j.talanta.2026.129666
Primary Topic
Biosensors and Analytical Detection
Type
article
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article

Chopped optical biosensing enables temporal background subtraction for high-sensitivity fluorescence immunoassays

Yair Noam, Ma Thi Huyen, Linoy Golani-Zaidie, Ravit Koren et al.
Talanta
Biosensors and Analytical Detection
article

Chopped optical biosensing enables temporal background subtraction for high-sensitivity fluorescence immunoassays

Yair Noam, Ma Thi Huyen, Linoy Golani-Zaidie, Ravit Koren, Yaniv Lustig, Tran Mai Hoa, Amos Danielli, Eli Schwartz, Victoria Indenbaum, Shmuel Burg, Meir Cohen, Sophie Terenteva, Tong Thi Kim Tuyen, Yossi Yossef Teboul, Le Thi Hoi, Nguyen Vu Trung, Reut Ashkenazy, Nguyen Minh Hoan
article en

Abstract

Fluorescence-based immunoassays are widely used for sensitive biomarker detection, but their performance at low analyte concentrations is often limited by background signals originating from unbound fluorophores, Raman scattering, and sample autofluorescence. Here, we introduce chopped optical biosensing (COB), an analytical framework that improves fluorescence immunoassay sensitivity by temporally separating background and target fluorescence. In COB, fluorophore-labeled targets captured on magnetic beads are concentrated into a small detection region using a permanent magnet. An optical chopper periodically gates the excitation beam, enabling fluorescence measurements before bead aggregation (background only) and after aggregation (target + background). Subtraction of these temporally separated signals isolates fluorescence from bead-bound targets while suppressing background contributions from unbound fluorophores, Raman scattering, and sample autofluorescence. By limiting continuous illumination, this approach also reduces photobleaching and stabilizes excitation intensity, while eliminating the need for washing steps or dynamic optical modulation. Analytical evaluation demonstrated detection limits of 61 fM for Atto 532 dye, 0.05 ng/L for interleukin-8 (IL-8), and 3 ng/mL for anti-dengue virus serotype 2 non-structural protein 1 (anti-DENV-2 NS1) immunoglobulin G (IgG), with reproducibility below 15%. The total assay time is approximately 90 min. In a targeted feasibility assessment using 64 well-characterized serum samples, the COB-based anti-DENV-2 NS1 IgG assay correctly classified all samples when compared with reference ELISA results. Combining low complexity, compact design, and energy-efficient operation with high analytical and clinical performance, COB provides a practical foundation for streamlined fluorescence immunoassay workflows and is well suited for future portable diagnostic applications.

TalantaVol. 305
Bar-Ilan University (IL), Hanoi Medical University (VN), Sheba Medical Center (IL), Israel Ministry of Health (IL), Institut Pasteur in Ho Chi Minh City (VN)
Affordable and clean energy
Openalex Percentile: Top 26%
Biosensors and Analytical Detection
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