Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation.
Federica De GaetanoMaria Chiara CristianoValentina VenutiVincenza CrupiDomenico MajolinoGiuseppe PaladiniGiuseppe AcriBarbara TestagrossaAlessia IrreraDonatella PaolinoSilvana TommasiniCinzia Anna VenturaRosanna StancanelliPublished in: Molecules (Basel, Switzerland) (2021)
This study was aimed at preparing and characterizing solid lipid nanoparticles loading rutin (RT-SLNs) for the treatment of oxidative stress-induced diseases. Phospholipon 80H® as a solid lipid and Polysorbate 80 as surfactant were used for the SLNs preparation, using the solvent emulsification/diffusion method. We obtained spherical RT-SLNs with low sizes, ranging from 40 to 60 nm (hydrodynamic radius) for the SLNs prepared starting from 2% and 5% (w/w) theoretical amount. All prepared formulations showed negative zeta-potential values. RT was efficiently encapsulated within SLNs, obtaining high encapsulation efficiency and drug content percentages, particularly for SLNs prepared with a 5% theoretical amount of RT. In vitro release profiles and analysis of the obtained data applying different kinetic models revealed Fickian diffusion as the main mechanism of RT release from the SLNs. The morphology of RT-SLNs was characterized by scanning electron microscopy (SEM), whereas the interactions between RT and the lipid matrix were investigated by Raman spectroscopy, evidencing spectral modifications of characteristic bands of RT due to the establishment of new interactions. Finally, antioxidant activity assay on human glioblastoma astrocytoma (U373) culture cells showed a dose-dependent activity for RT-SLNs, particularly at the highest assayed dose (50 μM), whereas the free drug showed the lesser activity.
Keyphrases
- electron microscopy
- fatty acid
- endothelial cells
- drug delivery
- high throughput
- machine learning
- magnetic resonance
- computed tomography
- emergency department
- risk assessment
- ionic liquid
- electronic health record
- single cell
- deep learning
- drug induced
- single molecule
- climate change
- liquid chromatography
- replacement therapy