Abstract
The efficacy of nanoparticle-mediated drug delivery is limited by its peri-vascular sequestration, thus necessitating a strategy to trigger drug release from such intra-tumoral nanocarrier-drug depots. In our efforts to explore remotely-activated nanocarriers, we have developed carbon nanocapsules comprised of an ultra-short carbon nanotube shell (US-tubes) loaded with cisplatin (CDDP@US-tubes) and covered with a Pluronic surfactant wrapping to minimize passive release. We demonstrate here that non-invasive radiofrequency (RF) field activation of the CDDP@US-tubes produces heat that causes Pluronic disruption which triggers cisplatin release in an RF-dependent manner. Furthermore, release-dependent cytotoxicity is demonstrated in human hepatocellular carcinoma cell lines.
Original language | English (US) |
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Pages (from-to) | 1862-1869 |
Number of pages | 8 |
Journal | Biomaterials |
Volume | 34 |
Issue number | 7 |
DOIs | |
State | Published - Feb 2013 |
Keywords
- Carbon nanotubes
- Cisplatin
- Liver cancer
- Radiofrequency field
- Triggered release
- US-tubes
ASJC Scopus subject areas
- Biophysics
- Bioengineering
- Ceramics and Composites
- Biomaterials
- Mechanics of Materials