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A bioactivated in vivo assembly nanotechnology fabricated NIR probe for small pancreatic tumor intraoperative imaging

Author

Listed:
  • Han Ren

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST))

  • Xiang-Zhong Zeng

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST)
    University of Chinese Academy of Sciences (UCAS)
    Peking University)

  • Xiao-Xiao Zhao

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST))

  • Da-yong Hou

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST)
    Department of Urology, The Fourth Hospital of Harbin Medical University, Heilongjiang Key Laboratory of Scientific Research in Urology
    Harbin Medical University)

  • Haodong Yao

    (Institute of High Energy Physics, Chinese Academy of Sciences (CAS))

  • Muhammad Yaseen

    (University of Peshawar)

  • Lina Zhao

    (Institute of High Energy Physics, Chinese Academy of Sciences (CAS))

  • Wan-hai Xu

    (Department of Urology, The Fourth Hospital of Harbin Medical University, Heilongjiang Key Laboratory of Scientific Research in Urology
    Harbin Medical University)

  • Hao Wang

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST))

  • Li-Li Li

    (CAS Center for Excellence in Nanoscience, CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology (NCNST))

Abstract

Real-time imaging of the tumour boundary is important during surgery to ensure that sufficient tumour tissue has been removed. However, the current fluorescence probes for bioimaging suffer from poor tumour specificity and narrow application of the imaging window used. Here, we report a bioactivated in vivo assembly (BIVA) nanotechnology, demonstrating a general optical probe with enhanced tumour accumulation and prolonged imaging window. The BIVA probe exhibits active targeting and assembly induced retention effect, which improves selectivity to tumours. The surface specific nanofiber assembly on the tumour surface increases the accumulation of probe at the boundary of the tumor. The blood circulation time of the BIVA probe is prolonged by 110 min compared to idocyanine green. The assembly induced metabolic stability broaden the difference between the tumor and background, obtaining a delayed imaging window between 8–96 h with better signal-to-background contrast (>9 folds). The fabricated BIVA probe permits precise imaging of small sized (

Suggested Citation

  • Han Ren & Xiang-Zhong Zeng & Xiao-Xiao Zhao & Da-yong Hou & Haodong Yao & Muhammad Yaseen & Lina Zhao & Wan-hai Xu & Hao Wang & Li-Li Li, 2022. "A bioactivated in vivo assembly nanotechnology fabricated NIR probe for small pancreatic tumor intraoperative imaging," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27932-y
    DOI: 10.1038/s41467-021-27932-y
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    References listed on IDEAS

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    1. Peiyuan Wang & Yong Fan & Lingfei Lu & Lu Liu & Lingling Fan & Mengyao Zhao & Yang Xie & Congjian Xu & Fan Zhang, 2018. "NIR-II nanoprobes in-vivo assembly to improve image-guided surgery for metastatic ovarian cancer," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
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    Cited by:

    1. Weiqi Zhang & Yinghua Zeng & Qiuqun Xiao & Yuanyuan Wu & Jiale Liu & Haocheng Wang & Yuting Luo & Jie Zhan & Ning Liao & Yanbin Cai, 2024. "An in-situ peptide-antibody self-assembly to block CD47 and CD24 signaling enhances macrophage-mediated phagocytosis and anti-tumor immune responses," Nature Communications, Nature, vol. 15(1), pages 1-19, December.

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