生物芯片
多路复用
外体
材料科学
纳米技术
微泡
注意事项
小RNA
生物信息学
生物
护理部
基因
医学
生物化学
作者
Yang Xu,Zeying Zhang,Yuanbin Wu,Huadong Wang,Yun Yang,Yali Sun,Hongfei Xie,Bogdan Bogdanov,Pavel Senyushkin,Jimei Chi,Zewei Lian,Dongdong Wu,Meng Su,Yanlin Song
标识
DOI:10.1002/adma.202304935
摘要
Abstract Rapid detection of various exosomes is of great significance in early diagnosis and postoperative monitoring of cancers. Here, a divisional optical biochip is reported for multiplex exosome analysis via combining the self‐assembly of nanochains and precise surface patterning. Arising from resonance‐induced near‐field enhancement, the nanochains show distinct color changes after capturing target exosomes for direct visual detection. Then, a series of divisional nanochain‐based biochips conjugated with several specific antibodies are fabricated through designed hydrophilic and hydrophobic patterns. Because of the significant wettability difference, one sample droplet is precisely self‐splitting into several microdroplets enabling simultaneous identification of multiple target exosomes in 30 min with a sensitivity of 6 × 10 7 particles mL −1 , which is about two orders lower than enzyme‐linked immunosorbent assay. Apart from the trace amount detection, excellent semiquantitative capability is demonstrated to distinguish clinical exosomes from glioblastoma patients and healthy people. This method is simple, versatile, and highly efficient that can be extended as a diagnostic tool for many diseases, promoting the development of liquid biopsy.
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