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Printed Divisional Optical Biochip for Multiplex Visualizable Exosome Analysis at Point-Of-Care.

Xu YangZeying ZhangYuanbin WuHuadong WangYang YunYali SunHongfei XieBogdan BogdanovPavel SenyushkinJimei ChiZewei LianDongdong WuMeng SuYanlin Song
Published in: Advanced materials (Deerfield Beach, Fla.) (2023)
Rapid detection of various exosomes is of great significance in early diagnosis and postoperative monitoring of cancers. Here, we report a divisional optical biochip 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 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, 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. This article is protected by copyright. All rights reserved.
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