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Author Spotlight: Advancing Research in Corneal Opacity Treatment and Regeneration
Published on: August 4, 2023
Fenofibrate microemulsion eyedrops for treating nitrogen mustard induced corneal injury
Ehsan Kaffash1, Rudra Pangeni1, Wentao Liang2
1Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Abstract:
Vesicants are highly toxic chemicals used as warfare agents, primarily absorbed through the skin, inhalation, or ocular surface. Nitrogen mustard (NM), a potent vesicant, often leads to blindness due to the inadequacies of existing therapies. This study explores the role of peroxisome proliferator-activated receptor-α (PPARα) in NM-induced ocular injury and evaluates the efficacy of fenofibrate (Feno), a PPARα agonist, in preventing corneal injury progression. Feno, an FDA-approved oral medication used to treat dyslipidemia, has shown off-labelled potential in promoting corneal wound healing. However, its limited ocular distribution following oral administration reduces its therapeutic efficacy. We developed Feno-loaded oil-in-water microemulsion (Feno ME) eyedrop formulations to enhance aqueous solubility and ocular bioavailability of Feno, aiming to improve the therapeutic efficacy in treating NM-induced corneal injury. Feno ME exhibited a mean droplet size of approximately 20 nm, remained physically stable for at least twelve months, showed prolonged ocular retention, and demonstrated well-accepted rheological properties without inducing ocular irritation or toxicity. Furthermore, Feno ME demonstrated sustained drug levels in ocular tissues with minimal systemic absorption. A 14-day treatment with 0.5% Feno ME (3×/day) significantly reduced corneal-ulceration, neovascularization (NV), and opacity in NM-induced ocular injury in rats. Histopathological analysis confirmed preserved corneal integrity and reduced inflammation. Immunohistochemistry revealed that NM injury significantly reduced PPARα levels in the corneal epithelium, which was restored with Feno ME eyedrop treatment, suggesting PPARα as a promising drug target for NM-induced corneal injury. Our Feno ME eyedrop formulation represents an effective topical delivery platform that effectively mitigates NM-induced corneal injury and offers a novel therapeutic strategy for vesicant exposure.
Insights
New fenofibrate microemulsion (Feno ME) eyedrops protect against nitrogen mustard (NM) ocular injury. This PPARα agonist formulation enhances drug delivery, reducing corneal damage and inflammation for vesicant exposure treatment.
Area of Science:
- Ophthalmology
- Pharmacology
- Materials Science
Background:
- Vesicant warfare agents, like nitrogen mustard (NM), cause severe ocular injury, often leading to blindness.
- Current therapies for NM-induced corneal damage are inadequate.
- Peroxisome proliferator-activated receptor-α (PPARα) plays a role in NM-induced ocular injury, and its agonist, fenofibrate (Feno), shows therapeutic potential.
Purpose of the Study:
- To investigate the role of PPARα in NM-induced ocular injury.
- To evaluate the efficacy of a novel fenofibrate-loaded microemulsion (Feno ME) eyedrop formulation in preventing and treating NM-induced corneal injury.
- To enhance ocular bioavailability and therapeutic efficacy of fenofibrate for vesicant exposure.
Main Methods:
- Development of Feno-loaded oil-in-water microemulsion (Feno ME) eyedrops.
- Characterization of Feno ME for droplet size, stability, rheology, and ocular compatibility.
- Evaluation of Feno ME efficacy in a rat model of NM-induced ocular injury, assessing corneal ulceration, neovascularization, and opacity.
- Histopathological and immunohistochemical analyses to confirm corneal integrity, inflammation, and PPARα expression.
Main Results:
- Feno ME eyedrops exhibited optimal physicochemical properties (approx. 20nm droplet size, 12-month stability) and good ocular retention with minimal systemic absorption.
- Topical treatment with 0.5% Feno ME significantly reduced corneal ulceration, neovascularization, and opacity in NM-injured rats.
- Histopathology confirmed preserved corneal structure and reduced inflammation; immunohistochemistry showed Feno ME restored NM-reduced corneal epithelial PPARα levels.
Conclusions:
- PPARα is a viable therapeutic target for NM-induced corneal injury.
- The developed Feno ME eyedrop formulation effectively delivers fenofibrate to the eye, mitigating NM-induced corneal damage.
- Feno ME eyedrops offer a promising, novel therapeutic strategy for treating vesicant chemical exposure injuries to the eye.
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