Topical Amphotericin B Semisolid Dosage Form for Cutaneous Leishmaniasis: Physicochemical Characterization, Ex Vivo Skin Permeation and Biological Activity

dc.contributor.author
Berenguer, Diana
dc.contributor.author
Alcover Amengual, Maria Magdalena
dc.contributor.author
Sessa, Marcella
dc.contributor.author
Halbaut, Lyda
dc.contributor.author
Guillen, Carmen
dc.contributor.author
Boix Montañés, Antonio de Pádua
dc.contributor.author
Fisa Saladrigas, Roser
dc.contributor.author
Calpena Campmany, Ana Cristina
dc.contributor.author
Riera Lizandra, Ma. Cristina
dc.contributor.author
Sosa Díaz, Lilian Elisa
dc.date.issued
2020-02-24T16:33:24Z
dc.date.issued
2020-02-24T16:33:24Z
dc.date.issued
2020-02-12
dc.date.issued
2020-02-24T16:33:24Z
dc.identifier
1999-4923
dc.identifier
https://hdl.handle.net/2445/151046
dc.identifier
695971
dc.identifier
32059430
dc.description.abstract
Amphotericin B (AmB) is a potent antifungal successfully used intravenously to treat visceral leishmaniasis but depending on the Leishmania infecting species, it is not always recommended against cutaneous leishmaniasis (CL). To address the need for alternative topical treatments of CL, the aim of this study was to elaborate and characterize an AmB gel. The physicochemical properties, stability, rheology and in vivo tolerance were assayed. Release and permeation studies were performed on nylon membranes and human skin, respectively. Toxicity was evaluated in macrophage and keratinocyte cell lines, and the activity against promastigotes and intracellular amastigotes of Leishmania infantum was studied. The AmB gel remained stable for a period of two months, with optimal properties for topical use and no apparent toxic effect on the cell lines. High amounts of AmB were found in damaged and non‐damaged skin (1230.10 ± 331.52 and 2484.57 ± 439.12 μg/g/cm2, respectively) and they were above the IC50 of AmB for amastigotes. Although there were no differences in the in vitro anti‐leishmanial activity between the AmB solution and gel, the formulation resulted in a higher amount of AmB being retained in the skin, and is therefore a candidate for further studies of in vivo efficacy.
dc.format
16 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
MDPI
dc.relation
Reproducció del document publicat a: https://doi.org/10.3390/pharmaceutics12020149
dc.relation
Pharmaceutics, 2020, vol. 12, num. 2, p. 149
dc.relation
https://doi.org/10.3390/pharmaceutics12020149
dc.rights
cc-by (c) Berenguer, Diana et al., 2020
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biologia, Sanitat i Medi Ambient)
dc.subject
Leishmania infantum
dc.subject
Utilització de medicaments
dc.subject
Leishmania infantum
dc.subject
Drug utilization
dc.title
Topical Amphotericin B Semisolid Dosage Form for Cutaneous Leishmaniasis: Physicochemical Characterization, Ex Vivo Skin Permeation and Biological Activity
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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