Development of novel biopolymer-based nanoparticles loaded cream for potential treatment of topical fungal infections

Biodegradable polymers are extensively used due to their efficient safety profiles. The aim of the current study was to fabricate, evaluate, and characterize biodegradable, biocompatible fluconazole (FLZ) loaded chitosan (CHS) chondroitin sulfate (CS) nanoparticles (NPs) for topical delivery. Polyme...

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Veröffentlicht in:Drug development and industrial pharmacy 2021-07, Vol.47 (7), p.1090-1099
Hauptverfasser: Khalid, Aimen, Ahmed, Naveed, Qindeel, Maimoona, Asad, Muhammad Imran, Khan, Gul Majid, ur.Rehman, Asim
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Sprache:eng
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Zusammenfassung:Biodegradable polymers are extensively used due to their efficient safety profiles. The aim of the current study was to fabricate, evaluate, and characterize biodegradable, biocompatible fluconazole (FLZ) loaded chitosan (CHS) chondroitin sulfate (CS) nanoparticles (NPs) for topical delivery. Polymers utilized in the formulation not only served as a carrier system but also aided in fighting with complex etiology of the disease due to their innate antifungal activities. NPs were prepared by the complex coacervation method, then were optimized for various parameters and subsequently loaded into a cream. Scanning electron microscopic (SEM) analysis showed spherical morphology of the NPs. Prepared NPs showed an average particle size in the range of 350-450 nm and an encapsulation efficiency (EE) of 86%. The polydispersity index (PDI) was found to be 0.148 that showed a uniform distribution of NPs. Fourier transform infrared (FTIR) spectroscopy confirmed the absence of any electrostatic interaction between ingredients. In vitro drug release analyses exhibited a sustained release of the drug and higher antifungal activity than free FLZ. Ex vivo permeability and drug distribution in different skin layers ensured a site-specific delivery of the FLZ-NPs. As compared with free FLZ and other control groups, the prepared NPs also exhibited significantly higher antifungal activity against Candida albicans (p 
ISSN:0363-9045
1520-5762
DOI:10.1080/03639045.2021.1957914