Literature DB >> 29154484

Memantine-Loaded PEGylated Biodegradable Nanoparticles for the Treatment of Glaucoma.

Elena Sánchez-López1,2, Maria Antonia Egea1, Benjamin Michael Davis3, Li Guo3, Marta Espina1, Amelia Maria Silva4, Ana Cristina Calpena1, Eliana Maria Barbosa Souto5, Nivedita Ravindran3, Miren Ettcheto2,6, Antonio Camins2,6, Maria Luisa García1, Maria Francesca Cordeiro3,7.   

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.
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  PLGA-PEG; drug delivery; glaucoma; memantine; nanoparticles

Mesh:

Substances:

Year:  2017        PMID: 29154484     DOI: 10.1002/smll.201701808

Source DB:  PubMed          Journal:  Small        ISSN: 1613-6810            Impact factor:   13.281


  19 in total

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