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Transscleral Delivery of Dexamethasone-Loaded Microparticles Using a Dissolving Microneedle Array
Rawan Fitaihi1, Shorooq Abukhamees1, Mine Orlu1
1Research Department of Pharmaceutics, School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Pharmaceutics
|June 28, 2023
Summary
This study introduces dissolvable microneedles for ocular drug delivery. These microneedles effectively deliver dexamethasone to the sclera and posterior eye, offering a convenient, minimally invasive option.
Area of Science:
- Ophthalmology
- Biomaterials Science
- Drug Delivery Systems
Background:
- Ocular drug delivery faces challenges due to biological barriers.
- Microneedles (MNs) offer a promising approach for overcoming these barriers.
- Dexamethasone (Dex) is a corticosteroid used for various ocular conditions.
Purpose of the Study:
- To develop and evaluate a novel dissolvable microneedle array for ocular drug delivery.
- To achieve controlled transscleral delivery of dexamethasone using PLGA microparticles.
- To assess the efficacy and safety of the microneedle system for posterior eye drug deposition.
Main Methods:
- Formulation of dissolvable microneedles loaded with dexamethasone-PLGA microparticles.
- Mechanical testing of microneedles for scleral penetration capability (porcine model).
- Quantification of dexamethasone permeation through the sclera and distribution within the ocular globe.
Main Results:
- Microneedles demonstrated sufficient strength for porcine scleral penetration.
- Dexamethasone permeation was significantly higher compared to topical delivery.
- 19.2% of administered dexamethasone reached the vitreous humour, with microparticle diffusion confirmed in the sclera.
Conclusions:
- The developed microneedle system enables minimally invasive, controlled dexamethasone delivery to the posterior eye.
- This approach offers improved drug bioavailability and patient convenience through self-administration.
- Dissolvable microneedles represent a viable strategy for enhancing ocular drug delivery efficacy.

