Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies

被引:8
作者
Uroro, Evelyn Osehontue [1 ]
Bright, Richard [2 ]
Hayles, Andrew [2 ]
Vasilev, Krasimir [1 ,2 ]
机构
[1] Univ South Australia, UniSA STEM, Mawson Lakes, SA 5095, Australia
[2] Flinders Univ S Australia, Coll Med & Publ Hlth, Bedford Pk, SA 5042, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
amphotericin B; polycaprolactone (PCL); lipase; drug delivery; cytocompatible; antifungal activity; CANDIDA-ALBICANS; IN-VITRO; SUSTAINED-RELEASE; FUNGAL-INFECTIONS; SYSTEM;
D O I
10.3390/nano13010155
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
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页数:14
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