Size dependency of PLGA-nanoparticle uptake and antifungal activity against Aspergillus flavus

被引:1
|
作者
Patel, Nipur R. [1 ]
Damann, Kenneth [1 ]
Leonardi, Claudia [1 ]
Sabliov, Cristina M. [1 ]
机构
[1] Louisiana State Univ, Ctr Agr, Baton Rouge, LA 70803 USA
关键词
antifungal; Aspergillus flavus; internalization; itraconazole; nanoparticles; penetration; PLGA; polylactic-co-glycolic acid; uptake; DRUG-DELIVERY; PARTICLE-SIZE; BIODEGRADABLE NANOPARTICLES; POLY(DL-LACTIDE-CO-GLYCOLIDE) NANOPARTICLES; AMPHOTERICIN-B; ORAL DELIVERY; RELEASE; ITRACONAZOLE; SYSTEMS; MICROPARTICLES;
D O I
10.2217/NNM.11.35
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Itraconazole and coumarin-6 loaded polylactic-co-glycolic acid-nanoparticles (PLGA-ITZ-and PLGA-C6-NPs) were synthesized and tested for fungal cell uptake and antifungal ability based on particle size. Materials & Methods: PLGA-ITZ-and PLGA-C6-NPs were synthesized using an oil-in-water emulsion evaporation method. Fungal cell uptake and antifungal activity of the polymeric NPs was tested on Aspergillus flavus. Results: PLGA-C6-NPs of 203 nm associated with fungal cell surfaces and internalized efficiently, while 1206 nm NPs associated with cell surfaces were internalized less efficiently. Antifungal studies of PLGA-ITZ-NPs of 232, 630 and 1060 nm showed differences in inhibitory activity with 232 nm NPs showing superior activity at the lowest ITZ concentration of 0.003 mg/ml, followed by 630 and 1060 nm NPs. No differences in antifungal activity were observed at higher ITZ concentrations. Conclusion: The PLGA-ITZ-NP system can increase bioavailability of ITZ by improving its aqueous dispersibility and efficiently delivering ITZ to fungal cells via endocytosis.
引用
收藏
页码:1381 / 1395
页数:15
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