In-Situ Thermoresponsive Hydrogel Containing Resveratrol-Loaded Nanoparticles as a Localized Drug Delivery Platform for Dry Eye Disease

• Published in: Antioxidants 2023-04, Vol.12 (5), p.993
• Main Authors: De Luca, Ilenia, Di Cristo, Francesca, Conte, Raffaele, Peluso, Gianfranco, Cerruti, Pierfrancesco, Calarco, Anna
• Format: Article
• Language: English
• Subjects: acetylated nanoparticles; antioxidant; Antioxidants; Bioavailability; Biocompatibility; Controlled release; Cornea; Drug delivery; Drug delivery systems; Drugs; Efficiency; Epithelial cells; epithelial corneal cells; Eye diseases; eye dry disease; Health aspects; hydrogel; Hydrogels; Inflammation; Mitochondria; Nanoparticles; Older people; Osmotic pressure; Oxidative stress; Phase transitions; Polyethylene glycol; Polyethyleneimine; Polylactide-co-glycolide; Polymers; Polyphenols; Polyvinyl alcohol; Quality of life; Resveratrol; SIRT1 protein; Tumor necrosis factor-TNF; Vehicles; Viscosity
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox12050993

Dry eye disease (DED) is a dynamic and complex disease that can cause significant damage to the ocular surface and discomfort, compromising the patient's quality of life. Phytochemicals such as resveratrol have received increasing attention due to their ability to interfere with multiple pathways related to these diseases. However, the low bioavailability and the poor therapeutic response of resveratrol hinder its clinical applications. Cationic polymeric nanoparticles, in combination with in situ gelling polymers, could represent a promising strategy to prolong drug corneal residence time reducing the frequency of administration and increasing the therapeutic response. Eyedrop formulations, based on acetylated polyethyleneimine-modified polylactic-co-glicolyc acid- (PLGA-PEI) nanoparticles loaded with resveratrol (RSV-NPs) were dispersed into poloxamer 407 hydrogel and characterized in terms of pH, gelation time, rheological properties, in vitro drugs release, and biocompatibility. Moreover, the antioxidant and anti-inflammatory effects of RSV were assessed in vitro by mimicking a DED condition through the exposition of epithelial corneal cells to a hyperosmotic state. This formulation exhibited sustained release of RSV for up to 3 days, exerting potent antioxidant and anti-inflammatory effects on corneal epithelial cells. In addition, RSV reversed the mitochondrial dysfunction mediated by high osmotic pressure, leading to upregulated sirtuin-1 (SIRT1) expression, an essential regulator of mitochondrial function. These results suggest the potential of eyedrop formulation as a platform to overcome the rapid clearance of current solutions for treating various inflammation- and oxidative stress-related diseases such as DED.