Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions

Detalhes bibliográficos
Autor(a) principal: Hennemann, Bruno Luís
Data de Publicação: 2022
Outros Autores: Bender, Caroline Raquel, Moleta, Guilherme Scalcão, Carvalho, Anderson Ramos, Bazana, Luana Candice Genz, Fuentefria, Alexandre Meneghello, Frizzo, Clarissa Piccinin
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/253603
Resumo: This research reports accelerated stability experiments, the evaluation of intermolecular interactions, and antifungal assays for fluconazole emulsions prepared using ultrasound (US) and magnetic stirring (MS) in the presence of ionic liquids derived from 1,n-(3-methylimidazolium-1- yl)alkane bromide ([CnMIM]Br; n = 12 or 16). The goals of the investigation are to quantify the stability, identify the forces that drive the formation and stability, and determine the antifungal activity of fluconazole-containing emulsions, and corroborate the data from our previous results that indicated that the emulsion based on [C16MIM]Br seemed to be more stable. In this study, accelerated stability experiments evidenced a considerable stability for the [C16MIM]Br emulsions at two temperatures (25 and 37 C)—the instability index increased in the following order: US40% < US20% < MS. The 1H NMR data showed that the ILs interacts differently with medium-chain triglycerides (MCT). Two distinct interaction mechanisms were also observed for [C12MIM]Br and [C16MIM]Br with fluconazole, in which the latter formed more compact mixed aggregates than the former. The result was corroborated by diffusion data, which showed that ILs suffered a decrease in diffusion in the presence of fluconazole. The antifungal assay showed that emulsions containing ILs displayed superior activity compared with fluconazole alone. The emulsions also showed potent activity in inhibiting a resistant species (C. glabrata—CG34) to FLZ. All emulsions showed weak irritant potential in HET-CAM assay.
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spelling Hennemann, Bruno LuísBender, Caroline RaquelMoleta, Guilherme ScalcãoCarvalho, Anderson RamosBazana, Luana Candice GenzFuentefria, Alexandre MeneghelloFrizzo, Clarissa Piccinin2023-01-12T04:56:15Z20221999-4923http://hdl.handle.net/10183/253603001159480This research reports accelerated stability experiments, the evaluation of intermolecular interactions, and antifungal assays for fluconazole emulsions prepared using ultrasound (US) and magnetic stirring (MS) in the presence of ionic liquids derived from 1,n-(3-methylimidazolium-1- yl)alkane bromide ([CnMIM]Br; n = 12 or 16). The goals of the investigation are to quantify the stability, identify the forces that drive the formation and stability, and determine the antifungal activity of fluconazole-containing emulsions, and corroborate the data from our previous results that indicated that the emulsion based on [C16MIM]Br seemed to be more stable. In this study, accelerated stability experiments evidenced a considerable stability for the [C16MIM]Br emulsions at two temperatures (25 and 37 C)—the instability index increased in the following order: US40% < US20% < MS. The 1H NMR data showed that the ILs interacts differently with medium-chain triglycerides (MCT). Two distinct interaction mechanisms were also observed for [C12MIM]Br and [C16MIM]Br with fluconazole, in which the latter formed more compact mixed aggregates than the former. The result was corroborated by diffusion data, which showed that ILs suffered a decrease in diffusion in the presence of fluconazole. The antifungal assay showed that emulsions containing ILs displayed superior activity compared with fluconazole alone. The emulsions also showed potent activity in inhibiting a resistant species (C. glabrata—CG34) to FLZ. All emulsions showed weak irritant potential in HET-CAM assay.application/pdfengPharmaceutics. Basel. Vol. 14, n. 4 (2022), 710, 18 p.AntifúngicosFluconazolLíquidos iônicosIonic liquidUltrasoundEmulsionFluconazoleIntermolecular interactionAntifungal activityAntifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactionsEstrangeiroinfo: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:UFRGSTEXT001159480.pdf.txt001159480.pdf.txtExtracted Texttext/plain73227http://www.lume.ufrgs.br/bitstream/10183/253603/2/001159480.pdf.txt523259f60e91b947919b74d1467ce7b1MD52ORIGINAL001159480.pdfTexto completo (inglês)application/pdf5308375http://www.lume.ufrgs.br/bitstream/10183/253603/1/001159480.pdf6d833a5e96ed4f18b2e4f2d75f15710bMD5110183/2536032023-01-13 06:03:36.993858oai:www.lume.ufrgs.br:10183/253603Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-01-13T08:03:36Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
title Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
spellingShingle Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
Hennemann, Bruno Luís
Antifúngicos
Fluconazol
Líquidos iônicos
Ionic liquid
Ultrasound
Emulsion
Fluconazole
Intermolecular interaction
Antifungal activity
title_short Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
title_full Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
title_fullStr Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
title_full_unstemmed Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
title_sort Antifungal activity and stability of fluconazole emulsion containing ionic liquids explained by intermolecular interactions
author Hennemann, Bruno Luís
author_facet Hennemann, Bruno Luís
Bender, Caroline Raquel
Moleta, Guilherme Scalcão
Carvalho, Anderson Ramos
Bazana, Luana Candice Genz
Fuentefria, Alexandre Meneghello
Frizzo, Clarissa Piccinin
author_role author
author2 Bender, Caroline Raquel
Moleta, Guilherme Scalcão
Carvalho, Anderson Ramos
Bazana, Luana Candice Genz
Fuentefria, Alexandre Meneghello
Frizzo, Clarissa Piccinin
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Hennemann, Bruno Luís
Bender, Caroline Raquel
Moleta, Guilherme Scalcão
Carvalho, Anderson Ramos
Bazana, Luana Candice Genz
Fuentefria, Alexandre Meneghello
Frizzo, Clarissa Piccinin
dc.subject.por.fl_str_mv Antifúngicos
Fluconazol
Líquidos iônicos
topic Antifúngicos
Fluconazol
Líquidos iônicos
Ionic liquid
Ultrasound
Emulsion
Fluconazole
Intermolecular interaction
Antifungal activity
dc.subject.eng.fl_str_mv Ionic liquid
Ultrasound
Emulsion
Fluconazole
Intermolecular interaction
Antifungal activity
description This research reports accelerated stability experiments, the evaluation of intermolecular interactions, and antifungal assays for fluconazole emulsions prepared using ultrasound (US) and magnetic stirring (MS) in the presence of ionic liquids derived from 1,n-(3-methylimidazolium-1- yl)alkane bromide ([CnMIM]Br; n = 12 or 16). The goals of the investigation are to quantify the stability, identify the forces that drive the formation and stability, and determine the antifungal activity of fluconazole-containing emulsions, and corroborate the data from our previous results that indicated that the emulsion based on [C16MIM]Br seemed to be more stable. In this study, accelerated stability experiments evidenced a considerable stability for the [C16MIM]Br emulsions at two temperatures (25 and 37 C)—the instability index increased in the following order: US40% < US20% < MS. The 1H NMR data showed that the ILs interacts differently with medium-chain triglycerides (MCT). Two distinct interaction mechanisms were also observed for [C12MIM]Br and [C16MIM]Br with fluconazole, in which the latter formed more compact mixed aggregates than the former. The result was corroborated by diffusion data, which showed that ILs suffered a decrease in diffusion in the presence of fluconazole. The antifungal assay showed that emulsions containing ILs displayed superior activity compared with fluconazole alone. The emulsions also showed potent activity in inhibiting a resistant species (C. glabrata—CG34) to FLZ. All emulsions showed weak irritant potential in HET-CAM assay.
publishDate 2022
dc.date.issued.fl_str_mv 2022
dc.date.accessioned.fl_str_mv 2023-01-12T04:56:15Z
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/253603
dc.identifier.issn.pt_BR.fl_str_mv 1999-4923
dc.identifier.nrb.pt_BR.fl_str_mv 001159480
identifier_str_mv 1999-4923
001159480
url http://hdl.handle.net/10183/253603
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Pharmaceutics. Basel. Vol. 14, n. 4 (2022), 710, 18 p.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
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