唾液
纳米传感器
癌症
癌症检测
高分子
计算生物学
放射性检测
材料科学
纳米技术
酶
化学
癌细胞
生物化学
癌症生物标志物
生物
离子键合
检出限
分子生物学
亚细胞定位
癌症研究
生物物理学
限制
淋巴结
癌症治疗
癌症治疗
作者
Nuo Chen,Dawei Li,Bo Hu,Wenxing Chen,Congcong Zhu,Xiang‐Yu Kong,Wen Li,Xuliang Deng,Yan Wei
标识
DOI:10.1002/adma.202522747
摘要
ABSTRACT Saliva assay is a promising potential strategy for widespread screening and prompt surveillance of oral cancer to improve the prognosis and reduce the financial burden. But current saliva detection methods are hampered from clinical application by their restricted target diversity, complex procedures, and costly equipment. In this work, we introduce an enzymatic responsive serial‐nanofluids strategy, enabling simultaneous trace‐level detection of multiple humoral markers in saliva. Enzymatic‐responsive nanochannels were engineered respectively by modifying the outer surfaces of AAO arrays with polypeptides featuring target‐cleavage sites. Thus, the macromolecular markers in saliva could cleave corresponding polypeptide, opening the ion pathway and enhancing the ion flux of nanochannels. Upon the open of a set of nanochannel‐arrays tandemly connected, serial‐nanofluids are generated and ionic currents are coupled to enable collaborative detection of multiple targets. Employing oral cancer markers of MMP‐1 and MMP‐3 as models, we developed a mobile nanosensor that can concurrently monitor their trace variation low to 2.14 × 10 − 1 3 g/mL. Furthermore, the clinical trial indicated that our nanosensor could noninvasively, conveniently, and effectively distinguish healthy individuals from oral cancer patients, and those with lymph node metastasis. This strategy offers a robust framework for multi‐marker detection in clinical diagnostics, facilitating high‐frequency and large‐scale cancer screening through saliva test.
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