Microstructured Optical Fiber-Enhanced Light-Matter Interaction Enables Highly Sensitive Exosome-Based Liquid Biopsy of Breast Cancer

被引:23
作者
Liu, Zihao [1 ]
Zhang, Wen [2 ]
Zhang, Xin [3 ]
Wang, Shijia [1 ]
Xia, Zhiwen [1 ]
Guo, Xiaoyan [1 ]
Zhao, Yu [4 ,5 ,6 ]
Wang, Pu [3 ,5 ,6 ]
Wang, Xiu-Hong [1 ,5 ,6 ]
机构
[1] Beijing Univ Technol, Lab Biomed Photon, Beijing 100124, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, Dept Immunol, Natl Clin Res Ctr Canc,Canc Hosp, Beijing 100021, Peoples R China
[3] Beijing Univ Technol, Lab Adv Laser Technol & Applicat, Beijing 100124, Peoples R China
[4] Beijing Univ Technol, Inst Laser Engn, Fac Mat & Mfg, Lab Adv Photon, Beijing 100124, Peoples R China
[5] Minist Educ, Key Lab Transscale Laser Mfg Technol, Beijing 100124, Peoples R China
[6] Beijing Engn Res Ctr Laser Technol, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
EXTRACELLULAR VESICLES; GOLD NANOPARTICLES; MUCIN; BIOSENSOR;
D O I
10.1021/acs.analchem.2c03794
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Exosome-based liquid biopsies highlight potential utility in diagnosis and determining the prognosis of patients with cancer and other diseases. However, the existing techniques are severely limited for practical applications due to the complications of high cost, low sensitivity, tedious procedures, and large sample consumption. Herein, we report a microstructured optical fiber sensor for fast, sensitive, and accurate quantification of exosomes in blood samples of breast cancer patients. Numerical simulations are applied to demonstrate that hollow-core microstructured anti-resonant fibers (HARFs) can stringently confine light in the fiber core, ensuring strong light-matter interaction and thus maximumly amplifying the signal. Taking this advantage, a AuNPs-dsDNA assembly containing gold nanoparticles, a recognizing DNA aptamer, and a fluorescent reporter DNA sequence is fabricated followed by immobilization on the fiber wall to form a AuNPs- dsDNA-HARF sensor. Cancer-derived exosomes can be recognized and captured in the fiber channel and generate dose-dependent fluorescent signals for quantification. The microfiber sensor demonstrates enhanced sensitivity and specificity, enabling the detection of single digits of exosome particles at the nanoliter sample level. In addition, by tracking exosome phenotypic changes, the proposed fiber sensor can facilitate precise drug treatment monitoring. This work provides a robust platform for exosome-based biopsy for cancer diagnosis and prediction of therapeutic outcomes.
引用
收藏
页码:1095 / 1105
页数:11
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