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Hyaluronic acid conjugated magnetic prussian blue@quantum dot nanoparticles for cancer theranostics

  • Yongbo Yang
  • , Lijia Jing
  • , Xiaoda Li
  • , Li Lin
  • , Xiuli Yue*
  • , Zhifei Dai
  • *Corresponding author for this work
  • School of Life Science and Technology, Harbin Institute of Technology
  • Peking University

Research output: Contribution to journalArticlepeer-review

Abstract

A multifunctional nanotheranostic agent was developed by conjugating both hyaluronic acid and bovine serum albumin coated CuInS2-ZnS quantum dots onto the surface of magnetic Prussian blue nanoparticles. The obtained nanoagent could serve as an efficient contrast agent to simultaneously enhance near infrared (NIR) fluorescence and magnetic resonance (MR) imaging greatly. The coexistence of magnetic core and CD44 ligand hyaluronic acid was found to largely improve the specific uptake of the nanoagent by CD44 overexpressed HeLa cells upon applying an external magnetic field. Both NIR fluorescence and MR imaging in vivo proved high accumulation of the nanoagent at tumor site due to its excellent CD44 receptor/magnetic dual targeting capability. After intravenous injection of the nanoagent and treatment of external magnetic field, the tumor in nude mice was efficiently ablated upon NIR laser irradiation and the tumor growth inhibition was more than 89.95%. Such nanotheranostic agent is of crucial importance for accurately identifying the size and location of the tumor before therapy, monitoring the photothermal treatment procedure in real-time during therapy, assessing the effectiveness after therapy.

Original languageEnglish
Article number411
JournalTheranostics
Volume7
Issue number2
DOIs
StatePublished - 2017

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

  • Bimodal Imaging
  • Fe3O4 nanoparticles
  • Photothermal therapy
  • Prussian blue nanoparticles
  • Quantum Dots
  • Tumor targeting

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