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Antifungal Effect of Liposomal α-Bisabolol and When Associated with Fluconazole

Authors :
Camila F. Bezerra
José Geraldo de A. Júnior
Rosilaine de L. Honorato
Antonia Thassya L. dos Santos
Josefa Carolaine P. da Silva
Taís G. da Silva
Thiago S. de Freitas
Thiago Adler T. Vieira
Maria Clara F. Bezerra
Débora Lima Sales
João Pedro V. Rodrigues
José M. Barbosa Filho
Laisla R. Peixoto
Allyson P. Pinheiro
Henrique D. M. Coutinho
Maria Flaviana B. Morais-Braga
Teresinha G. da Silva
Source :
Cosmetics, Vol 8, Iss 2, p 28 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Fungal pathologies caused by the genus Candida have increased in recent years due to the involvement of immunosuppressed people and the advance of resistance mechanisms acquired by these microorganisms. Liposomes are nanovesicles with lipid bilayers in which they store compounds. α-Bisabolol is a sesquiterpene with proven biological activities, and in this work it was tested alone in liposomes and in association with Fluconazole in vitro to evaluate the antifungal potential, Fluconazole optimization, and virulence inhibitory effect in vitro. Antifungal assays were performed against standard strains of Candida albicans, Candida tropicalis, and Candida krusei by microdilution to identify the IC50 values and to obtain the cell viability. The Minimum Fungicidal Concentration (MFC) was performed by subculturing on the solid medium, and at their subinhibitory concentration (Matrix Concentration (MC): 16,384 µg/mL) (MC/16), the compounds, both isolated and liposomal, were associated with fluconazole in order to verify the inhibitory effect of this junction. Tests to ascertain changes in morphology were performed in microculture chambers according to MC concentrations. Liposomes were characterized from the vesicle size, polydispersity index, average Zeta potential, and scanning electron microscopy. The IC50 value of the liposomal bisabolol associated with fluconazole (FCZ) was 2.5 µg/mL against all strains tested, revealing a potentiating effect. Liposomal bisabolol was able to potentiate the effect of fluconazole against the CA and CT strains by reducing its concentration and completely inhibiting fungal growth. α-Bisabolol in liposomal form inhibited the morphological transition in all strains tested at a concentration of MC/8. The liposomes were homogeneous, with vesicles with diameters of 203.8 nm for the liposomal bisabolol and a surface charge potential of −34.2 mV, conferring stability to the nanosystem. Through scanning microscopy, the spherical shapes of the vesicles were observed.

Details

Language :
English
ISSN :
20799284
Volume :
8
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Cosmetics
Publication Type :
Academic Journal
Accession number :
edsdoj.b9c2907a8e9b4db892465f6bc7b12d1c
Document Type :
article
Full Text :
https://doi.org/10.3390/cosmetics8020028