Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design

Detalhes bibliográficos
Autor(a) principal: Mattos, Cristiane Bastos de
Data de Publicação: 2015
Outros Autores: Argenta, Débora Fretes, Melchiades, Gabriela de Lima, Cordeiro, Marlon N. S., Tonini, Maiko L., Moraes, Milene H. de, Weber, Tanara Beatriz, Roman, Silvane Souza, Nunes, Ricardo José, Teixeira, Helder Ferreira, Steindel, Mário, Koester, Leticia Scherer
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/140191
Resumo: Nanoemulsions are drug delivery systems that may increase the penetration of lipophilic compounds through the skin, enhancing their topical effect. Chalcones are compounds of low water solubility that have been described as promising molecules for the treatment of cutaneous leishmaniasis (CL). In this context, the aim of this work was to optimize the development of a nanoemulsion containing a synthetic chalcone for CL treatment using a 22 full factorial design. The formulations were prepared by spontaneous emulsification and the experimental design studied the influence of two independent variables (type of surfactant – soybean lecithin or sorbitan monooleate and type of co-surfactants – polysorbate 20 or polysorbate 80) on the physicochemical characteristics of the nanoemulsions, as well as on the skin permeation/retention of the synthetic chalcone in porcine skin. In order to evaluate the stability of the systems, the antileishmanial assay was performed against Leishmania amazonensis 24 hours and 60 days after the preparation of the nanoemulsions. The formulation composed of soybean lecithin and polysorbate 20 presented suitable physicochemical characteristics (droplet size 171.9 nm; polydispersity index 0.14; zeta potential -39.43 mV; pH 5.16; and viscosity 2.00 cP), drug content (91.09%) and the highest retention in dermis (3.03 μg⋅g-1) – the main response of interest – confirmed by confocal microscopy. This formulation also presented better stability of leishmanicidal activity in vitro against L. amazonensis amastigote forms (half maximal inhibitory concentration value 0.32±0.05 μM), which confirmed the potential of the nanoemulsion soybean lecithin and polysorbate 20 for CL treatment.
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spelling Mattos, Cristiane Bastos deArgenta, Débora FretesMelchiades, Gabriela de LimaCordeiro, Marlon N. S.Tonini, Maiko L.Moraes, Milene H. deWeber, Tanara BeatrizRoman, Silvane SouzaNunes, Ricardo JoséTeixeira, Helder FerreiraSteindel, MárioKoester, Leticia Scherer2016-05-04T02:07:55Z20151178-2013http://hdl.handle.net/10183/140191000985480Nanoemulsions are drug delivery systems that may increase the penetration of lipophilic compounds through the skin, enhancing their topical effect. Chalcones are compounds of low water solubility that have been described as promising molecules for the treatment of cutaneous leishmaniasis (CL). In this context, the aim of this work was to optimize the development of a nanoemulsion containing a synthetic chalcone for CL treatment using a 22 full factorial design. The formulations were prepared by spontaneous emulsification and the experimental design studied the influence of two independent variables (type of surfactant – soybean lecithin or sorbitan monooleate and type of co-surfactants – polysorbate 20 or polysorbate 80) on the physicochemical characteristics of the nanoemulsions, as well as on the skin permeation/retention of the synthetic chalcone in porcine skin. In order to evaluate the stability of the systems, the antileishmanial assay was performed against Leishmania amazonensis 24 hours and 60 days after the preparation of the nanoemulsions. The formulation composed of soybean lecithin and polysorbate 20 presented suitable physicochemical characteristics (droplet size 171.9 nm; polydispersity index 0.14; zeta potential -39.43 mV; pH 5.16; and viscosity 2.00 cP), drug content (91.09%) and the highest retention in dermis (3.03 μg⋅g-1) – the main response of interest – confirmed by confocal microscopy. This formulation also presented better stability of leishmanicidal activity in vitro against L. amazonensis amastigote forms (half maximal inhibitory concentration value 0.32±0.05 μM), which confirmed the potential of the nanoemulsion soybean lecithin and polysorbate 20 for CL treatment.application/pdfengInternational Journal of Nanomedicine. Auckland, Dove Medical. Vol. 10 (2015), p. 5529-5542FarmáciaLeishmaniasisChalconeNanoemulsionFull factorialSkin permeationNanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial designEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000985480.pdf000985480.pdfTexto completo (inglês)application/pdf3784660http://www.lume.ufrgs.br/bitstream/10183/140191/1/000985480.pdf5aa788f69145ae85eb004a28241c8d25MD51TEXT000985480.pdf.txt000985480.pdf.txtExtracted Texttext/plain54605http://www.lume.ufrgs.br/bitstream/10183/140191/2/000985480.pdf.txta921c3c2a8865aa6675c605e7a93d0e2MD52THUMBNAIL000985480.pdf.jpg000985480.pdf.jpgGenerated Thumbnailimage/jpeg2042http://www.lume.ufrgs.br/bitstream/10183/140191/3/000985480.pdf.jpg18159cc2cf0e25c5ad55ace0205a1cecMD5310183/1401912021-09-18 04:54:38.712699oai:www.lume.ufrgs.br:10183/140191Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:54:38Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
title Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
spellingShingle Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
Mattos, Cristiane Bastos de
Farmácia
Leishmaniasis
Chalcone
Nanoemulsion
Full factorial
Skin permeation
title_short Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
title_full Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
title_fullStr Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
title_full_unstemmed Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
title_sort Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
author Mattos, Cristiane Bastos de
author_facet Mattos, Cristiane Bastos de
Argenta, Débora Fretes
Melchiades, Gabriela de Lima
Cordeiro, Marlon N. S.
Tonini, Maiko L.
Moraes, Milene H. de
Weber, Tanara Beatriz
Roman, Silvane Souza
Nunes, Ricardo José
Teixeira, Helder Ferreira
Steindel, Mário
Koester, Leticia Scherer
author_role author
author2 Argenta, Débora Fretes
Melchiades, Gabriela de Lima
Cordeiro, Marlon N. S.
Tonini, Maiko L.
Moraes, Milene H. de
Weber, Tanara Beatriz
Roman, Silvane Souza
Nunes, Ricardo José
Teixeira, Helder Ferreira
Steindel, Mário
Koester, Leticia Scherer
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mattos, Cristiane Bastos de
Argenta, Débora Fretes
Melchiades, Gabriela de Lima
Cordeiro, Marlon N. S.
Tonini, Maiko L.
Moraes, Milene H. de
Weber, Tanara Beatriz
Roman, Silvane Souza
Nunes, Ricardo José
Teixeira, Helder Ferreira
Steindel, Mário
Koester, Leticia Scherer
dc.subject.por.fl_str_mv Farmácia
topic Farmácia
Leishmaniasis
Chalcone
Nanoemulsion
Full factorial
Skin permeation
dc.subject.eng.fl_str_mv Leishmaniasis
Chalcone
Nanoemulsion
Full factorial
Skin permeation
description Nanoemulsions are drug delivery systems that may increase the penetration of lipophilic compounds through the skin, enhancing their topical effect. Chalcones are compounds of low water solubility that have been described as promising molecules for the treatment of cutaneous leishmaniasis (CL). In this context, the aim of this work was to optimize the development of a nanoemulsion containing a synthetic chalcone for CL treatment using a 22 full factorial design. The formulations were prepared by spontaneous emulsification and the experimental design studied the influence of two independent variables (type of surfactant – soybean lecithin or sorbitan monooleate and type of co-surfactants – polysorbate 20 or polysorbate 80) on the physicochemical characteristics of the nanoemulsions, as well as on the skin permeation/retention of the synthetic chalcone in porcine skin. In order to evaluate the stability of the systems, the antileishmanial assay was performed against Leishmania amazonensis 24 hours and 60 days after the preparation of the nanoemulsions. The formulation composed of soybean lecithin and polysorbate 20 presented suitable physicochemical characteristics (droplet size 171.9 nm; polydispersity index 0.14; zeta potential -39.43 mV; pH 5.16; and viscosity 2.00 cP), drug content (91.09%) and the highest retention in dermis (3.03 μg⋅g-1) – the main response of interest – confirmed by confocal microscopy. This formulation also presented better stability of leishmanicidal activity in vitro against L. amazonensis amastigote forms (half maximal inhibitory concentration value 0.32±0.05 μM), which confirmed the potential of the nanoemulsion soybean lecithin and polysorbate 20 for CL treatment.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2016-05-04T02:07:55Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/140191
dc.identifier.issn.pt_BR.fl_str_mv 1178-2013
dc.identifier.nrb.pt_BR.fl_str_mv 000985480
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv International Journal of Nanomedicine. Auckland, Dove Medical. Vol. 10 (2015), p. 5529-5542
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