多路复用
多路复用
计算机科学
宽带
纳米光子学
人工智能
分割
图像传感器
量子点
计算机视觉
纳米传感器
鉴定(生物学)
动态范围
物理
可扩展性
干扰(通信)
机器视觉
生物传感器
纳米技术
光学
反射器(摄影)
电子工程
灵活性(工程)
小RNA
序列(生物学)
时分复用
光电子学
多光谱图像
图像分割
谐振器
作者
Bowen Fu,Dong Yang,Zhiyi Yuan,Zhongshu Xiong,Guocheng Fang,Tian Zhou,Xiyu Sun,Ningyuan Nie,Po‐Hao Tseng,Yu‐Cheng Chen
标识
DOI:10.1002/adma.202522938
摘要
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 −17 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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