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ROS-Responsive Polyprodrug Nanoparticles for Triggered Drug Delivery and Effective Cancer Therapy

  • Xiaoding Xu
  • , Phei Er Saw
  • , Wei Tao
  • , Yujing Li
  • , Xiaoyuan Ji
  • , Sushant Bhasin
  • , Yanlan Liu
  • , Dana Ayyash
  • , Jonathan Rasmussen
  • , Marc Huo
  • , Jinjun Shi*
  • , Omid C. Farokhzad
  • *Corresponding author for this work
  • Brigham and Women’s Hospital
  • King Abdulaziz University

Research output: Contribution to journalArticlepeer-review

Abstract

The application of nanoparticles (NPs) to drug delivery has led to the development of novel nanotherapeutics for the treatment of various diseases including cancer. However, clinical use of NP-mediated drug delivery has not always translated into improved survival of cancer patients, in part due to the suboptimal properties of NP platforms, such as premature drug leakage during preparation, storage, or blood circulation, lack of active targeting to tumor tissue and cells, and poor tissue penetration. Herein, an innovative reactive oxygen species (ROS)-responsive polyprodrug is reported that can self-assemble into stable NPs with high drug loading. This new NP platform is composed of the following key components: (i) polyprodrug inner core that can respond to ROS for triggered release of intact therapeutic molecules, (ii) polyethylene glycol (PEG) outer shell to prolong blood circulation; and (iii) surface-encoded internalizing RGD (iRGD) to enhance tumor targeting and tissue penetration. These targeted ROS-responsive polyprodrug NPs show significant inhibition of tumor cell growth both in vitro and in vivo.

Original languageEnglish
Article number1700141
JournalAdvanced Materials
Volume29
Issue number33
DOIs
Publication statusPublished - 6 Sept 2017
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

  • ROS-responsive
  • cancer therapy
  • polyprodrug
  • tumor penetrating
  • tumor targeting

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