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Metal–Organic Framework Assisted and Tumor Microenvironment Modulated Synergistic Image-Guided Photo-Chemo Therapy

  • Yuanbo Wang
  • , Wenbo Wu
  • , Duo Mao
  • , Cathleen Teh
  • , Bo Wang
  • , Bin Liu*
  • *Corresponding author for this work
  • National University of Singapore
  • Agency for Science, Technology and Research, Singapore
  • Beijing Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

The complex tumor microenvironment (TME) and nonspecific drug targeting limit the clinical efficacy of photodynamic therapy in combination with chemotherapy. Herein, a metal–organic framework (MOF) assisted strategy is reported that modulates TME by reducing tumor hypoxia and intracellular glutathione (GSH) and offers targeted delivery and controlled release of the trapped chemodrug. Platinum(IV)-diazido complex (Pt(IV)) is loaded inside a Cu(II) carboxylate-based MOF, MOF-199, and an aggregation-induced-emission photosensitizer, TBD, is conjugated to polyethylene glycol for encapsulating Pt(IV)-loaded MOF-199. Once the fabricated TBD-Pt(IV)@MOF-199 nanoparticles are internalized by cancer cells, MOF-199 consumes intracellular GSH and decomposes to fragments to release Pt(IV). Upon light irradiation, the released Pt(IV) generates O2 that relieves hypoxia and produces Pt(II)-based chemodrug inside cancer cells. Concomitantly, efficient reactive oxygen species generation and bright emission are afforded by TBD, resulting in synergistic image-guided photo-chemo therapy with enhanced efficacies and mitigated side effects.

Original languageEnglish
Article number2002431
JournalAdvanced Functional Materials
Volume30
Issue number28
DOIs
Publication statusPublished - 1 Jul 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

  • aggregation-induced emission
  • image-guided photo-chemo therapy
  • metal–organic frameworks
  • targeted drug release
  • tumor microenvironment regulation

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