Multilayered Sandwich Structure Sensor: Confinement‐Mediated H 2 O 2 Enrichment Strategy for Ultrasensitive and Long‐term Stable Prostate Cancer Biomarker Detection

肌氨酸 检出限 材料科学 过氧化氢 级联 重复性 化学 纳米技术 组合化学 色谱法 生物化学 氨基酸 甘氨酸
作者
Xin Yang,Zuyi Lu,Weixuan Wu,Jionghui Gu,Xueyan Wei,Qingshan Yang,Zhongfeng Shi,Liqin Zhou,Zhenxia Zhao,Zhongxing Zhao,Zhongxing Zhao,Zhongxing Zhao
出处
期刊:Small [Wiley]
卷期号:21 (40): e05472-e05472
标识
DOI:10.1002/smll.202505472
摘要

Sarcosine (Sar), a critical potential biomarker for prostate cancer (PCa), is primarily detected via enzyme cascade reactions involving sarcosine oxidase (SOx) and peroxidase. Nevertheless, the intermediate product hydrogen peroxide (H2O2) tends to diffuse to the bulk solution phase without entering subsequent reaction, leading to suboptimal detection sensitivity and compromised analytical performance. To tackle this challenge, a multilayered sandwich nanozyme cascade sensor (designated as Cu-MOF/Rf@BDC) is proposed through a confinement-mediated H2O2 enrichment strategy. Its innovative architecture spatially restricts the H2O2 diffusion while maintaining optimal reaction proximity, thereby enhancing the utilization efficiency of H2O2 by local concentration effects. The confined microenvironment ultimately achieves the ultrasensitive Sar detection with a 3.31 nmol L-1 detection limit (1-2 orders lower than previously reported methods). In clinical urine samples tested for Sar detection, the sensor exhibits strong consistency with commercial enzyme-linked immunosorbent assay (ELISA) kits, confirming the reliability of its analytical performance. Significantly, the sensor demonstrates a 3.6-fold shorter preparation time and 6.0-12.0-fold longer signal duration compared to ELISA kits. These dual advantages accelerate the detection process and improve efficiency for large-scale clinical screening of PCa biomarkers. Furthermore, the developed sensor exhibits exceptional selectivity and repeatability, underscoring its potential practicality in complex analytical matrices.
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