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Published on: September 12, 2014
Pathology-inspired collagen-binding thermosensitive micelle drops enable prolonged and efficient treatment of fungal
Maoyu Cai1,2, Haiping Zhong3,4, Xindi Wang1,2
1Clinical College of Ophthalmology, Tianjin Medical University, Tianjin, 300020, China.
Abstract:
Fungal keratitis (FK) is a challenging-to-manage blinding corneal infectious disease that often leads to severe sequelae, such as corneal leukoplakia regardless of curative care. Moreover, the unique anatomical structure and tear turnover of the eye significantly limit the bioavailability and therapeutic efficacy of traditional eye drops. Inspired by the unique pathological features of corneal ulcers, we report a thermosensitive multifunctional eye drop, designated PX-TA, based on a poloxamer (PX) and a collagen-adhesive tannic acid (TA), for prolonged and efficient treatment of FK. PX-TA transforms into a gel at body temperature and adheres to exposed collagen at the ulcer site; this significantly improves the corneal retention time and bioavailability. PX-TA maintains corneal retention for at least 90 min, substantially exceeding both the 15-min limit of commercial mucoadhesive eye drops and the 30-min threshold of conventional in situ gels. When loaded with amphotericin B (AmB), once-daily PX-TA-AmB administration effectively suppresses inflammation and corneal scarring, demonstrating superior efficacy over six-times-daily free AmB drops and a good safety profile. Mechanistic investigations reveal that PX-TA-AmB mediates its therapeutic effects through the MAPK6/PI3K/AKT signaling pathway. Moreover, the metal-chelating properties of TA inhibit the copper-dependent enzyme lysyl oxidase (LOX), resulting in reduced matrix fibrosis. Overall, the use of PX-TA-AmB drops represents a simplified yet effective strategy for the potential clinical management of FK, inspiring the design of eye drop formulations.
Insights
A new thermosensitive eye drop, PX-TA, improves drug delivery for fungal keratitis (FK). This formulation enhances corneal retention and therapeutic efficacy, offering a simplified treatment strategy for this blinding eye infection.
Area of Science:
- Ophthalmology
- Materials Science
- Pharmacology
Background:
- Fungal keratitis (FK) is a severe corneal infection leading to blindness, with limited treatment efficacy due to poor eye drop bioavailability.
- The eye's anatomy and tear turnover hinder conventional drug delivery, necessitating advanced formulations for effective FK management.
Purpose of the Study:
- To develop a thermosensitive, multifunctional eye drop (PX-TA) for prolonged and efficient treatment of fungal keratitis.
- To enhance corneal retention time and drug bioavailability compared to existing eye drop formulations.
Main Methods:
- Formulation of a thermosensitive hydrogel (PX-TA) using poloxamer (PX) and tannic acid (TA).
- Evaluation of corneal retention time and in vitro/in vivo efficacy of PX-TA loaded with amphotericin B (AmB).
- Investigation of therapeutic mechanisms involving MAPK6/PI3K/AKT signaling and lysyl oxidase (LOX) inhibition.
Main Results:
- PX-TA demonstrated prolonged corneal retention (≥90 min), significantly exceeding commercial eye drops.
- Once-daily PX-TA-AmB effectively suppressed inflammation and corneal scarring, outperforming frequent free AmB administration.
- The formulation showed a favorable safety profile and elucidated therapeutic mechanisms, including matrix fibrosis reduction.
Conclusions:
- PX-TA-AmB offers a simplified, effective strategy for fungal keratitis management by enhancing drug delivery and therapeutic outcomes.
- This thermosensitive hydrogel approach holds promise for developing improved ophthalmic drug formulations.
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