Intelligent nanogels with self-adaptive responsiveness for improved tumor drug delivery and augmented chemotherapy

X. Li, H.L. Li, C.C. Zhang, A. Pich*, L.X. Xing*, X.Y. Shi*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

For cancer nanomedicine, the main goal is to deliver therapeutic agents effectively to solid tumors. Here, we report the unique design of self-adaptive ultrafast charge-reversible chitosan-polypyrrole nanogels (CH-PPy NGs) for enhanced tumor delivery and augmented chemotherapy. CH was first grafted with PPy to form CH-PPy polymers that were used to form CH-PPy NGs through glutaraldehyde cross-linking via a miniemulsion method. The CH-PPy NGs could be finely treated with an alkaline solution to generate ultrafast charge-reversible CH-PPy-OH-4 NGs (R-NGs) with a negative charge at a physiological pH and a positive charge at a slightly acidic pH. The R-NGs display good cytocompatibility, excellent protein resistance, and high doxorubicin (DOX) loading efficiency. Encouragingly, the prepared R-NGs/DOX have prolonged blood circulation time, enhanced tumor accumulation, penetration and tumor cell uptake due to their self-adaptive charge switching to be positively charged, and responsive drug delivery for augmented chemotherapy of ovarian carcinoma in vivo. Notably, the tumor accumulation of R-NGs/DOX (around 4.7%) is much higher than the average tumor accumulation of other nanocarriers (less than 1%) reported elsewhere. The developed self-adaptive PPy-grafted CH NGs represent one of the advanced designs of nanomedicine that could be used for augmented antitumor therapy with low side effects.
Original languageEnglish
Pages (from-to)3473-3484
Number of pages12
JournalBioactive Materials
Volume6
Issue number10
DOIs
Publication statusPublished - 1 Oct 2021

Keywords

  • Ultrafast charge conversion
  • Nanogels
  • Active transportation
  • Deep tumor penetration
  • Enhanced antitumor activity
  • NANOPARTICLES
  • NANOMEDICINE
  • NANOPLATFORM
  • PENETRATION
  • CELLS
  • MICROENVIRONMENT
  • TRANSCYTOSIS
  • DEGRADATION
  • STRATEGIES
  • DENDRIMERS

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