Abstract
Aim: To investigate the potential of modified solid lipid nanoparticles (SLN) for the delivery of paclitaxel (PAX). Materials & methods: SLN loaded with PAX were prepared via modified high-pressure hot homogenization. Formulation parameters were optimized to obtain a high-quality delivery system. SLN cores were coated, layer-by-layer, with a chitosan and hyaluronan (HA) shell. Selectivity toward HA receptors was tested in a breast cancer cell line, MCF-7. Results: Stable and reproducible nano-sized and negatively charged nanoparticles resulted. Findings reveal that chitosan-HA-coated SLN facilitated the targeting, cellular uptake and the time-/dose-controlled delivery and release of PAX, enhancing intrinsic chemotherapeutic activities. Conclusion: SLN are suitable carrier candidates for nano-oncology given their localized, and potent cytotoxic potential overcoming multidrug-resistant cancer cells.
Original language | American English |
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Pages (from-to) | 473-490 |
Number of pages | 18 |
Journal | Nanomedicine |
Volume | 12 |
Issue number | 5 |
DOIs | |
State | Published - 1 Mar 2017 |
Keywords
- chitosan
- drug delivery
- hyaluronan
- layer-by-layer
- multidrug resistance
- nanoncology
- paclitaxel
- solid lipid nanoparticles