Resumen
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.
Idioma original | Inglés estadounidense |
---|---|
Páginas (desde-hasta) | 473-490 |
Número de páginas | 18 |
Publicación | Nanomedicine |
Volumen | 12 |
N.º | 5 |
DOI | |
Estado | Publicada - 1 mar. 2017 |
Palabras clave
- chitosan
- drug delivery
- hyaluronan
- layer-by-layer
- multidrug resistance
- nanoncology
- paclitaxel
- solid lipid nanoparticles