循环肿瘤细胞
石墨烯
材料科学
微流控
光纤
光子学
液体活检
纳米技术
纤维
光电子学
生物医学工程
计算机科学
癌症
医学
内科学
复合材料
转移
电信
作者
Shuyuan Zhu,Li Chen,Xiaoyan Yin,Xiaoyan Guo,Wenjian Wu,Xiaotong Meng,Xin Zhang,Pu Wang,Xiuhong Wang
出处
期刊:Small
[Wiley]
日期:2025-08-29
标识
DOI:10.1002/smll.202505283
摘要
Abstract Metastatic spread in aggressive cancers is often initiated by circulating tumor cells (CTCs) before primary tumor detection. Current CTC analysis faces fundamental limitations due to extreme cell scarcity (≈10 cells mL −1 blood) and reliance on large sample volumes (>7.5 mL). To address these challenges, an integrated graphene oxide‐functionalized hollow‐core anti‐resonant fiber (HARF‐GO) platform is developed that combines: 1) enhanced photon‐matter interactions through optical confinement, enabling 700‐fold signal amplification compared to microplate assays without requiring external photonic components, and 2) intrinsic microfluidic capabilities for continuous processing of microliter‐scale samples. This “lab‐in‐fiber” system achieves exceptional sensitivity (2 CTCs/assay) using <1 mL serum within 1 h ‐ performance parameters that fully meet clinical CTC analysis requirements. Notably, captured cells maintain 94% viability after gentle elution with high‐ionic‐strength buffer, enabling robust downstream molecular analysis. By seamlessly integrating cell capture, enrichment, optical detection, and viable cell recovery in a single device, the technology overcomes critical limitations of current liquid biopsy methods, providing new capabilities for both minimal residual disease monitoring and precision oncology applications.
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