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 |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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ODS 3: Salud y bienestar
Palabras clave
- chitosan
- drug delivery
- hyaluronan
- layer-by-layer
- multidrug resistance
- nanoncology
- paclitaxel
- solid lipid nanoparticles
Huella
Profundice en los temas de investigación de 'Physicochemical characterization of chitosan-hyaluronan-coated solid lipid nanoparticles for the targeted delivery of paclitaxel: A proof-of-concept study in breast cancer cells'. En conjunto forman una huella única.Citar esto
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