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Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
Evelyn Osehontue Uroro1, Richard Bright2, Andrew Hayles2
1UniSA STEM, University of South Australia, Mawson Lakes, SA 5095, Australia.
Abstract:
Amphotericin B is an antifungal drug used for the treatment of invasive fungal infections. However, its clinical use is limited due to its serious side effects, such as renal and cardiovascular toxicity. Furthermore, amphotericin B is administered in high doses due to its poor water solubility. Hence, it is necessary to develop an on-demand release strategy for the delivery of amphotericin B to reduce cytotoxicity. The present report describes a novel encapsulation of amphotericin B into lipase-sensitive polycaprolactone to form a nanocomposite. Nanocomposites were produced by the oil-in-water method and their physicochemical properties such as size, hydrodynamic diameter, drug loading, and zeta potential were determined. The in vitro release of amphotericin B was characterized in the presence and absence of lipase. The antifungal activity of the nanocomposites was verified against lipase-secreting Candida albicans, and cytotoxicity was tested against primary human dermal fibroblasts. In the absence of lipase, the release of amphotericin B from the nanocomposites was minimal. However, in the presence of lipase, an enzyme that is abundant at infection sites, a fungicidal concentration of amphotericin B was released from the nanocomposites. The antifungal activity of the nanocomposites showed an enhanced effect against the lipase-secreting fungus, Candida albicans, in comparison to the free drug at the same concentration. Furthermore, nanoencapsulation significantly reduced amphotericin B-related cytotoxicity compared to the free drug. The synthesized nanocomposites can serve as a potent carrier for the responsive delivery of amphotericin B in antifungal applications.
Insights
This study developed novel lipase-sensitive polycaprolactone nanocomposites for amphotericin B delivery. These nanocomposites enable on-demand drug release at infection sites, enhancing antifungal activity and reducing toxicity.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Pharmacology
Background:
- Amphotericin B is a critical antifungal agent but suffers from dose-limiting toxicities and poor solubility.
- Current limitations necessitate innovative drug delivery systems for improved therapeutic outcomes.
Purpose of the Study:
- To develop a novel nanocomposite system for lipase-triggered, on-demand delivery of amphotericin B.
- To evaluate the antifungal efficacy and cytotoxicity of the developed nanocomposites.
Main Methods:
- Amphotericin B was encapsulated into lipase-sensitive polycaprolactone via an oil-in-water emulsion method.
- Nanocomposite physicochemical properties, in vitro drug release (with/without lipase), antifungal activity against Candida albicans, and cytotoxicity against human dermal fibroblasts were assessed.
Main Results:
- Nanocomposites demonstrated minimal amphotericin B release in the absence of lipase.
- Lipase triggered significant drug release, achieving fungicidal concentrations.
- Enhanced antifungal activity against Candida albicans and reduced cytotoxicity were observed compared to free amphotericin B.
Conclusions:
- Lipase-sensitive polycaprolactone nanocomposites offer a promising strategy for responsive amphotericin B delivery.
- This approach can improve antifungal treatment by targeting drug release and minimizing side effects.
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