Abstract
In drug delivery, carbon nanotubes (CNTs) hold a great potential as carriers because of their ability to easily cross biological barriers and be internalised into cells. Their high aspect ratio allows multi-functionalisation and their development as a multimodal platform for targeted therapy. In this article, we report the controlled covalent derivatisation of triple-functionalised CNTs with the anticancer drug gemcitabine, folic acid as a targeting ligand and fluorescein as a probe. The anticancer activity of gemcitabine was maintained after covalent grafting onto the CNTs. The functionalised nanotubes were internalised into both folate-positive and negative cells, suggesting the passive diffusion of CNTs. Overall, our approach is versatile and offers a precise chemical control of the sidewall functionalisation of CNTs and the possibility to manoeuvre the types of functionalities required on the nanotubes for a multimodal therapeutic strategy.
Original language | English |
---|---|
Pages (from-to) | 14886–14892 |
Journal | Chemistry: A European Journal |
Volume | 21 |
Issue number | 42 |
Early online date | 2 Sept 2015 |
DOIs | |
Publication status | Published - 12 Oct 2015 |
Keywords
- Cancer
- carbon nanotube
- Drug delivery
- fluorescent probe
- functionalization