Memantine‐Loaded PEGylated Biodegradable Nanoparticles for the Treatment of Glaucoma |
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Authors: | Elena Sánchez‐López Maria Antonia Egea Benjamin Michael Davis Li Guo Marta Espina Amelia Maria Silva Ana Cristina Calpena Eliana Maria Barbosa Souto Nivedita Ravindran Miren Ettcheto Antonio Camins Maria Luisa García Maria Francesca Cordeiro |
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Affiliation: | 1. Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy, Institute of Nanoscience and Nanotechnology (IN2UB), University of Barcelona, Barcelona, Spain;2. Biomedical Research and Networking Center in Neurodegenerative diseases (CIBERNED), Madrid, Spain;3. Glaucoma and Retinal Neurodegeneration Research, Visual Neuroscience, UCL Institute of Ophthalmology, London, UK;4. Department of Biology and Environment, School of Life and Environmental sciences (ECVA, UTAD), and Centre for Research and Technology of Agro‐Environmental and Biological Sciences (CITAB‐UTAD), University of Trás‐os‐Montes e Alto Douro, Vila Real, Portugal;5. Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra (FFUC) and REQUIMTE/Group of Pharmaceutical Technology, Coimbra, Portugal;6. Department of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy, University of Barcelona, Barcelona, Spain;7. Western Eye Hospital, Imperial College Healthcare Trust, London, UK |
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Abstract: | Glaucoma is a multifactorial neurodegenerative disease associated with retinal ganglion cells (RGC) loss. Increasing reports of similarities in glaucoma and other neurodegenerative conditions have led to speculation that therapies for brain neurodegenerative disorders may also have potential as glaucoma therapies. Memantine is an N‐methyl‐d ‐aspartate (NMDA) antagonist approved for Alzheimer's disease treatment. Glutamate‐induced excitotoxicity is implicated in glaucoma and NMDA receptor antagonism is advocated as a potential strategy for RGC preservation. This study describes the development of a topical formulation of memantine‐loaded PLGA‐PEG nanoparticles (MEM‐NP) and investigates the efficacy of this formulation using a well‐established glaucoma model. MEM‐NPs <200 nm in diameter and incorporating 4 mg mL?1 of memantine were prepared with 0.35 mg mL?1 localized to the aqueous interior. In vitro assessment indicated sustained release from MEM‐NPs and ex vivo ocular permeation studies demonstrated enhanced delivery. MEM‐NPs were additionally found to be well tolerated in vitro (human retinoblastoma cells) and in vivo (Draize test). Finally, when applied topically in a rodent model of ocular hypertension for three weeks, MEM‐NP eye drops were found to significantly (p < 0.0001) reduce RGC loss. These results suggest that topical MEM‐NP is safe, well tolerated, and, most promisingly, neuroprotective in an experimental glaucoma model. |
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Keywords: | drug delivery glaucoma memantine nanoparticles PLGA‐PEG |
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