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首页> 外文期刊>Sensors and Actuators >Triple-enhanced surface plasmon resonance spectroscopy based on cell membrane and folic acid functionalized gold nanoparticles for dual-selective circulating tumor cell sensing
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Triple-enhanced surface plasmon resonance spectroscopy based on cell membrane and folic acid functionalized gold nanoparticles for dual-selective circulating tumor cell sensing

机译:基于细胞膜和叶酸官能化金纳米颗粒的三重增强表面等离子体共振光谱,用于双选择性循环肿瘤细胞感测

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摘要

Circulating tumor cells (CTCs) are an important biomarker of cancer and are valuable in evaluating the risk of metastatic progression and in facilitating precise therapeutic treatments. In this paper, a dual-selective strategy was constructed to achieve the sensitive detection of CTCs. Cell membrane fragment-functionalized AuNPs (M-AuNPs) and folic acid-functionalized AuNPs (FA-AuNPs) were fabricated and characterized. CTCs membrane containing the specific junction plakoglobin (JUP) could be captured onto Anti-JUP-modified gold chip selectively. FA-AuNPs can bind with M-AuNPs through the overexpressed FA receptors in the CTCs membrane. These double selective recognitions through the specific interaction between JUP and Anti-JUP, FA and FA receptor can ensure the sensor's accuracy and specificity. The ultra-sensitive CTCs detection was achieved through multi-signal amplifications, including cell membrane fragments, M-AuNPs and FA-AuNPs. The biosensor constructed here has a low detection limit of 1 cell within the linear range of 10~1-10~5 cell mL~(-1). The low detection limit is in accordance with clinical detection standards. Owing to its outstanding selectivity, sensitivity, and stability, this new biosensor strategy for detecting CTCs offers new possibilities for clinical testing.
机译:循环肿瘤细胞(CTC)是癌症的重要生物标志物,并且在评估转移性进展的风险和促进精确治疗治疗方面是有价值的。本文构建了双选择性策略以实现CTC的敏感性检测。细胞膜片段官能化AUNPS(M-AUNP)和叶酸官能化的AUNPS(FA-AUNPS)制备并表征。可以选择性地捕获含有特定结吡胶蛋白(JUP)的CTCS膜。 FA-AUNP可以通过CTCS膜中的过表达FA受体与M-AUNP结合。这些双重选择性识别通过JUP和ANT-JUP之间的特定相互作用,FA和FA接收器可以确保传感器的准确性和特异性。通过多信号扩增实现超敏感的CTCS检测,包括细胞膜片段,M-AUNP和FA-AUNP。本文构建的生物传感器在10〜1-10〜5细胞m1〜(-1)的线性范围内的1个细胞的低检测限。低检测限符合临床检测标准。由于其出色的选择性,灵敏度和稳定性,这种用于检测CTC的新生物传感器策略为临床测试提供了新的可能性。

著录项

  • 来源
    《Sensors and Actuators》 |2020年第2期|127543.1-127543.8|共8页
  • 作者单位

    Center for Molecular Recognition and Biosensing School of Life Sciences Shanghai University Shanghai 200444 PR China;

    Center for Molecular Recognition and Biosensing School of Life Sciences Shanghai University Shanghai 200444 PR China;

    Center for Molecular Recognition and Biosensing School of Life Sciences Shanghai University Shanghai 200444 PR China Shanghai Key Laboratory of Bio-Energy Crop School of Life Sciences Shanghai University Shanghai 200444 PR China;

    Center for Molecular Recognition and Biosensing School of Life Sciences Shanghai University Shanghai 200444 PR China;

    Department of Chemistry Chungnam National University Daejeon 301-747 Republic of Korea;

    Institute of General Education Pusan National University Busan 609-735 Republic of Korea;

    Department of Oncology Shanghai Tenth People's Hospital Tongji University School of Medicine Shanghai 200072 PR China;

    Center for Molecular Recognition and Biosensing School of Life Sciences Shanghai University Shanghai 200444 PR China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Surface plasmon resonance; Circulating tumor cells; M-AuNPs; FA-AuNPs; Dual selective;

    机译:表面等离子体共振;循环肿瘤细胞;m-aunps;FA-AUNPS;双重选择性;

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