Broadband Nanocavity Imaging with Machine Vision for Multiplex miRNA Assays

Sensitive and multiplexed quantification of microRNAs (miRNAs) remains challenging due to their short length, low abundance, and sequence homology, particularly in complex biological matrices. This paper presents an approach that combines a distributed Bragg reflector (DBR)-coupled silver nanoparticle (AgNP) gap nanocavity with deep learning instance segmentation for automated image readout. Applied to A549 lung cancer cell extracts, the assay directly quantifies endogenous miR-191, miR-25, and miR-130a without enrichment or amplification. The nanocavity concentrates fields and favors radiative decay, enhancing collection and suppressing quantum dot (QD) blinking, while Mask R-CNN enables robust, high-throughput counting and classification. The system achieves an attomolar LOD (∼10<sup>-17</sup> mol/L), a linear dynamic range spanning five orders of magnitude, and >99% correct identification across spectrally encoded channels. These results establish an AI-enabled nanophotonic biosensing platform that is sensitive, specific, robust, and scalable for multiplexed miRNA analysis in research and clinically relevant matrices.

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Publication Details

Journal
Advanced Materials
Published
2026-02-25
DOI
https://doi.org/10.1002/adma.202522938
Primary Topic
Plasmonic and Surface Plasmon Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Broadband Nanocavity Imaging with Machine Vision for Multiplex miRNA Assays

Y. C. Chen, Ningyuan Nie, Zhongshu Xiong, T. Zhou et al.
Advanced Materials
Plasmonic and Surface Plasmon Research
article

Broadband Nanocavity Imaging with Machine Vision for Multiplex miRNA Assays

Y. C. Chen, Ningyuan Nie, Zhongshu Xiong, T. Zhou, Po-Hao Tseng, Dong Yang, Guocheng Fang, Xiyu Sun, Zhiyi Yuan, Bowen Fu
article en

Abstract

Sensitive and multiplexed quantification of microRNAs (miRNAs) remains challenging due to their short length, low abundance, and sequence homology, particularly in complex biological matrices. This paper presents an approach that combines a distributed Bragg reflector (DBR)-coupled silver nanoparticle (AgNP) gap nanocavity with deep learning instance segmentation for automated image readout. Applied to A549 lung cancer cell extracts, the assay directly quantifies endogenous miR-191, miR-25, and miR-130a without enrichment or amplification. The nanocavity concentrates fields and favors radiative decay, enhancing collection and suppressing quantum dot (QD) blinking, while Mask R-CNN enables robust, high-throughput counting and classification. The system achieves an attomolar LOD (∼10<sup>-17</sup> mol/L), a linear dynamic range spanning five orders of magnitude, and >99% correct identification across spectrally encoded channels. These results establish an AI-enabled nanophotonic biosensing platform that is sensitive, specific, robust, and scalable for multiplexed miRNA analysis in research and clinically relevant matrices.

Advanced MaterialsVol. 38(17)
Nanyang Technological University (SG)
Openalex Percentile: Top 44%
Plasmonic and Surface Plasmon Research
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