{"title":"Si Nanorod Array Integrated Microfluidic Device for Enhanced Extracellular Vesicle Isolation","authors":"Hanyue Kang, Cheng Li, Wenfei Liu, Tongqing Yang, Liang Ma, Na Sun, Xiaobin Xu","doi":"10.1002/admt.202400294","DOIUrl":null,"url":null,"abstract":"Tumor‐derived extracellular vesicles (EVs) have attracted tremendous interest as one of the early cancer diagnostic markers. The major obstacle preventing EV‐based liquid biopsy is the efficient collection of EVs from the complex body fluid environment. This paper introduces a nanorod‐integrated microfluidic chip capable of immunoaffinity‐isolating EVs. Periodic silicon nanorod arrays in zigzag channels are prepared by nanosphere lithography. Nanorod sidewalls provide larger binding sites for antibodies, and their close interspacing to the EV sizes improves the binding probability. The fluid simulation results show that the significant increase in isolation efficiency also comes from the liquid perturbation enhanced by the particular nanorod arrangement. Under optimal operating conditions, plasma samples from patients (<jats:italic>n</jats:italic> = 14) with different types of cancers (hepatocellular carcinoma, colorectal cancer, and pancreatic adenocarcinoma) to the chip for EV isolation is applied. In this proof‐of‐concept study, the expression level of the epidermal growth factor receptor (EGFR) in isolated EVs is then quantified using droplet digital PCR, showing good diagnostic performance in cancer detection.","PeriodicalId":7200,"journal":{"name":"Advanced Materials & Technologies","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials & Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/admt.202400294","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Tumor‐derived extracellular vesicles (EVs) have attracted tremendous interest as one of the early cancer diagnostic markers. The major obstacle preventing EV‐based liquid biopsy is the efficient collection of EVs from the complex body fluid environment. This paper introduces a nanorod‐integrated microfluidic chip capable of immunoaffinity‐isolating EVs. Periodic silicon nanorod arrays in zigzag channels are prepared by nanosphere lithography. Nanorod sidewalls provide larger binding sites for antibodies, and their close interspacing to the EV sizes improves the binding probability. The fluid simulation results show that the significant increase in isolation efficiency also comes from the liquid perturbation enhanced by the particular nanorod arrangement. Under optimal operating conditions, plasma samples from patients (n = 14) with different types of cancers (hepatocellular carcinoma, colorectal cancer, and pancreatic adenocarcinoma) to the chip for EV isolation is applied. In this proof‐of‐concept study, the expression level of the epidermal growth factor receptor (EGFR) in isolated EVs is then quantified using droplet digital PCR, showing good diagnostic performance in cancer detection.
肿瘤衍生的细胞外囊泡 (EV) 作为早期癌症诊断标志物之一,引起了人们的极大兴趣。阻碍基于 EV 的液体活检的主要障碍是如何从复杂的体液环境中有效收集 EV。本文介绍了一种能够免疫亲和性分离 EVs 的纳米棒集成微流控芯片。该芯片采用纳米光刻技术制备了人字形通道中的周期性硅纳米棒阵列。纳米棒侧壁为抗体提供了更大的结合位点,其与 EV 大小的紧密间隔提高了结合概率。流体模拟结果表明,隔离效率的显著提高还来自于特定纳米棒排列所增强的液体扰动。在最佳操作条件下,将来自不同类型癌症(肝细胞癌、结直肠癌和胰腺癌)患者(n = 14)的血浆样本应用到芯片上进行 EV 分离。在这项概念验证研究中,利用液滴数字 PCR 对分离出的 EV 中表皮生长因子受体 (EGFR) 的表达水平进行了量化,结果表明该芯片在癌症检测方面具有良好的诊断性能。