Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/molecules23082075 http://hdl.handle.net/11449/180152 |
Resumo: | Antimicrobial photodynamic therapy (aPDT) has been proposed as an alternative method for oral candidiasis (OC), while nanocarriers have been used to improve the water solubility of curcumin (CUR). The aim of this study is to encapsulate CUR in polymeric nanoparticles (NPs) and to evaluate its photodynamic effects on a murine model of OC. Anionic and cationic CUR-NP is synthesized using poly-lactic acid and dextran sulfate and then characterized. Female mice are immunosuppressed and inoculated with Candida albicans (Ca) to induce OC. aPDT is performed by applying CUR-NP or free CUR on the dorsum of the tongue, followed by blue light irradiation for five consecutive days. Nystatin is used as positive control. Afterward, Ca are recovered and cultivated. Animals are euthanized for histological, immunohistochemical, and DNA damage evaluation. Encapsulation in NP improves the water solubility of CUR. Nystatin shows the highest reduction of Ca, followed by aPDT mediated by free CUR, which results in immunolabelling of cytokeratins closer to those observed for healthy animals. Anionic CUR-NP does not show antifungal effect, and cationic CUR-NP reduces Ca even in the absence of light. DNA damage is associated with Ca infection. Consecutive aPDT application is a safe treatment for OC. |
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Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasisCandida albicansCurcuminKeratinsMiceNanoparticlesOral candidiasisPhotochemotherapyAntimicrobial photodynamic therapy (aPDT) has been proposed as an alternative method for oral candidiasis (OC), while nanocarriers have been used to improve the water solubility of curcumin (CUR). The aim of this study is to encapsulate CUR in polymeric nanoparticles (NPs) and to evaluate its photodynamic effects on a murine model of OC. Anionic and cationic CUR-NP is synthesized using poly-lactic acid and dextran sulfate and then characterized. Female mice are immunosuppressed and inoculated with Candida albicans (Ca) to induce OC. aPDT is performed by applying CUR-NP or free CUR on the dorsum of the tongue, followed by blue light irradiation for five consecutive days. Nystatin is used as positive control. Afterward, Ca are recovered and cultivated. Animals are euthanized for histological, immunohistochemical, and DNA damage evaluation. Encapsulation in NP improves the water solubility of CUR. Nystatin shows the highest reduction of Ca, followed by aPDT mediated by free CUR, which results in immunolabelling of cytokeratins closer to those observed for healthy animals. Anionic CUR-NP does not show antifungal effect, and cationic CUR-NP reduces Ca even in the absence of light. DNA damage is associated with Ca infection. Consecutive aPDT application is a safe treatment for OC.School of Dentistry São Paulo State University (UNESP)School of Pharmaceutical Sciences São Paulo State University (UNESP)School of Dentistry São Paulo State University (UNESP)School of Pharmaceutical Sciences São Paulo State University (UNESP)Universidade Estadual Paulista (Unesp)Sakima, Vinicius Tatsuyuji [UNESP]Barbugli, Paula Aboud [UNESP]Cerri, Paulo Sérgio [UNESP]Chorilli, Marlus [UNESP]Carmello, Juliana Cabrini [UNESP]Pavarina, Ana Cláudia [UNESP]De Oliveira Mima, Ewerton Garcia [UNESP]2018-12-11T17:38:23Z2018-12-11T17:38:23Z2018-08-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.3390/molecules23082075Molecules, v. 23, n. 8, 2018.1420-3049http://hdl.handle.net/11449/18015210.3390/molecules230820752-s2.0-850527844152-s2.0-85052784415.pdf327849591120788214271259967162820000-0001-5756-5828Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecules0,855info:eu-repo/semantics/openAccess2024-09-27T15:15:19Zoai:repositorio.unesp.br:11449/180152Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T15:15:19Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
title |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
spellingShingle |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis Sakima, Vinicius Tatsuyuji [UNESP] Candida albicans Curcumin Keratins Mice Nanoparticles Oral candidiasis Photochemotherapy |
title_short |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
title_full |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
title_fullStr |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
title_full_unstemmed |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
title_sort |
Antimicrobial photodynamic therapy mediated by curcumin-loaded polymeric nanoparticles in a murine model of oral candidiasis |
author |
Sakima, Vinicius Tatsuyuji [UNESP] |
author_facet |
Sakima, Vinicius Tatsuyuji [UNESP] Barbugli, Paula Aboud [UNESP] Cerri, Paulo Sérgio [UNESP] Chorilli, Marlus [UNESP] Carmello, Juliana Cabrini [UNESP] Pavarina, Ana Cláudia [UNESP] De Oliveira Mima, Ewerton Garcia [UNESP] |
author_role |
author |
author2 |
Barbugli, Paula Aboud [UNESP] Cerri, Paulo Sérgio [UNESP] Chorilli, Marlus [UNESP] Carmello, Juliana Cabrini [UNESP] Pavarina, Ana Cláudia [UNESP] De Oliveira Mima, Ewerton Garcia [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Sakima, Vinicius Tatsuyuji [UNESP] Barbugli, Paula Aboud [UNESP] Cerri, Paulo Sérgio [UNESP] Chorilli, Marlus [UNESP] Carmello, Juliana Cabrini [UNESP] Pavarina, Ana Cláudia [UNESP] De Oliveira Mima, Ewerton Garcia [UNESP] |
dc.subject.por.fl_str_mv |
Candida albicans Curcumin Keratins Mice Nanoparticles Oral candidiasis Photochemotherapy |
topic |
Candida albicans Curcumin Keratins Mice Nanoparticles Oral candidiasis Photochemotherapy |
description |
Antimicrobial photodynamic therapy (aPDT) has been proposed as an alternative method for oral candidiasis (OC), while nanocarriers have been used to improve the water solubility of curcumin (CUR). The aim of this study is to encapsulate CUR in polymeric nanoparticles (NPs) and to evaluate its photodynamic effects on a murine model of OC. Anionic and cationic CUR-NP is synthesized using poly-lactic acid and dextran sulfate and then characterized. Female mice are immunosuppressed and inoculated with Candida albicans (Ca) to induce OC. aPDT is performed by applying CUR-NP or free CUR on the dorsum of the tongue, followed by blue light irradiation for five consecutive days. Nystatin is used as positive control. Afterward, Ca are recovered and cultivated. Animals are euthanized for histological, immunohistochemical, and DNA damage evaluation. Encapsulation in NP improves the water solubility of CUR. Nystatin shows the highest reduction of Ca, followed by aPDT mediated by free CUR, which results in immunolabelling of cytokeratins closer to those observed for healthy animals. Anionic CUR-NP does not show antifungal effect, and cationic CUR-NP reduces Ca even in the absence of light. DNA damage is associated with Ca infection. Consecutive aPDT application is a safe treatment for OC. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:38:23Z 2018-12-11T17:38:23Z 2018-08-19 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/molecules23082075 Molecules, v. 23, n. 8, 2018. 1420-3049 http://hdl.handle.net/11449/180152 10.3390/molecules23082075 2-s2.0-85052784415 2-s2.0-85052784415.pdf 3278495911207882 1427125996716282 0000-0001-5756-5828 |
url |
http://dx.doi.org/10.3390/molecules23082075 http://hdl.handle.net/11449/180152 |
identifier_str_mv |
Molecules, v. 23, n. 8, 2018. 1420-3049 10.3390/molecules23082075 2-s2.0-85052784415 2-s2.0-85052784415.pdf 3278495911207882 1427125996716282 0000-0001-5756-5828 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Molecules 0,855 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1813546529610268672 |