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In vivo evaluation of a miniaturized fluorescence molecular tomography (Fmt) endoscope for breast cancer detection using targeted nanoprobes

  • Hao Yang
  • , Weipin Qian
  • , Lily Yang
  • , Huikai Xie
  • , Huabei Jiang*
  • *Corresponding author for this work
  • University of South Florida
  • Emory University
  • University of Florida

Research output: Contribution to journalArticlepeer-review

Abstract

In this study, in vivo animal experiments with 12 nude mice bearing breast-cancer-patient-tissue-derived xenograft (PDX) tumors were performed aiming to verify the imaging capability of a novel miniaturized fluorescence molecular tomography (FMT) endoscope, in combination with targeted nanoparticle–near-infrared (NIR) dye conjugates. Tumor-bearing mice were divided into two groups by systematic injection with urokinase plasminogen activator receptor-targeted (n = 7) and nontargeted (n = 5) imaging nanoprobes as a contrast agent, respectively. Each mouse was imaged at 6, 24, and 48 h following the injection of nanoprobes using the FMT endoscope. The results show that systemic delivery of targeted nanoprobes produced a 4-fold enhancement in fluorescence signals from tumors, compared with tumors that received nontargeted nanoprobes. This study indicates that our miniaturized FMT endoscope, coupled with the targeted nanoparticle– NIR dye conjugates as a contrast agent, has high sensitivity and specificity, and thus great potential to be used for image-guided detection and removal of a primary tumor and local metastatic tumors during surgery.

Original languageEnglish
Article number9389
Pages (from-to)1-10
Number of pages10
JournalInternational Journal of Molecular Sciences
Volume21
Issue number24
DOIs
Publication statusPublished - 2 Dec 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Breast cancer
  • Endoscope
  • Fluorescence molecular tomography
  • NIR dye
  • Nanoparticles
  • Patient-tissue-derived xenograft (PDX) tumor

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