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 language | English |
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Pages (from-to) | 3473-3484 |
Number of pages | 12 |
Journal | Bioactive Materials |
Volume | 6 |
Issue number | 10 |
DOIs | |
Publication status | Published - 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