Carboxymethylinulin-Chitosan Nanoparticles for the Delivery of Antineoplastic Mitoxantrone.
Daniele MerliFabrizio PiviAntonella ProfumoPaolo QuadrelliChiara MilaneseGiulia RisiLivia VisaiPublished in: ChemMedChem (2016)
Mitoxantrone (MTX) is an antineoplastic agent whose use is limited by serious side effects on non-neoplastic cells. The aim of this study was the development of a new drug release system using an ionotropic gelation technique for microencapsulation of MTX in chitosan-carboxymethylinulin nanoparticles (CCInp), followed by evaluation of their cytotoxic effects on neoplastic MDA-MB-231 and non-neoplastic NIH3T3 cell lines. The CCInp were prepared through a new reliable method for easy functionalization of both inulin and chitosan. Both unloaded and drug-loaded nanoparticles were characterized by transmission electron microscopy (TEM) and dynamic light scattering (DLS) and showed a spherical morphology with an average hydrodynamic diameter between 40 and 80 nm. Both nanoparticles were stable and easily degraded by lysozyme. MTX-loaded nanoparticles led to a greater mortality of MDA-MB-231 relative to free drug due to the ability of the nanoparticles to accumulate preferentially in neoplastic cells. The developed drug release system retains the ability to kill MDA-MB-231 cells in vitro, improving the survival of NIH3T3 cells.
Keyphrases
- drug delivery
- drug release
- cell cycle arrest
- induced apoptosis
- cell death
- pi k akt
- wound healing
- breast cancer cells
- walled carbon nanotubes
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- electron microscopy
- coronary artery disease
- type diabetes
- emergency department
- photodynamic therapy
- cardiovascular events
- cell proliferation
- drug induced
- free survival
- oxide nanoparticles