Nanoemulsions containing a synthetic chalcone as an alternative for treating cutaneous leshmaniasis : optimization using a full factorial design
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , , , |
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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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 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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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1178-2013 000985480 |
url |
http://hdl.handle.net/10183/140191 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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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openAccess |
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