化学
生物芯片
检出限
纳米技术
荧光
信号(编程语言)
分析物
光子学
光子晶体
灵敏度(控制系统)
光电子学
光学
物理
色谱法
计算机科学
电子工程
工程类
材料科学
程序设计语言
作者
Songlin Liu,Bochen Ma,Liqing Qi,Jiantao Ping,YuDong Che,Yimin Zhang,Meng Su,Yanlin Song,Lubin Qi,Yifei Jiang,Xiaohong Fang
标识
DOI:10.1021/acs.analchem.4c02863
摘要
The rapid and sensitive quantification of low-abundance protein markers holds immense significance in early disease diagnosis and treatment. Single-molecule fluorescence imaging exhibits very high detection sensitivity and thus has great application potential in this area. The single-molecule signal, however, is often susceptible to interference from background noise due to its inherently weak intensity. A variety of signal amplification techniques based on cascading reactions have been developed to improve the signal-to-noise ratio of single-molecule imaging. Nevertheless, the operation of these methods is typically complicated and time-consuming, which limits the clinical application. Herein, we introduce an enzyme-free, photonic-crystal-based single-molecule (PC-SM) biochip for cost-effective, time-efficient, and ultrasensitive detection of disease markers. The PC-SM biochip can enhance the signal-to-noise ratio of single molecules by nearly 3-fold compared with unamplified samples, through coupling of the single-molecule photon energy with the optical band gap of the photonic crystal. We used the PC-SM biochip to detect the low-abundance leukemia inhibitory factor in the blood of pancreatic cancer patients and healthy people and achieved a detection limit of 2.0 pg/L and an AUC of 0.9067. The method exhibits exceptional sensitivity and specificity, showing great application potential in various clinical settings.
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