How can micelle systems be rebuilt by a heating process?

Detalhes bibliográficos
Autor(a) principal: da Silva-Filho, Miguel Adelino
Data de Publicação: 2012
Outros Autores: Siqueira, Scheyla Daniela Vieira da Silva, Freire, Larissa Bandeira, de Araújo, Ivonete Batista, de Holandae e Silva, Káttya Gyselle, da Medeiros, Aldo Cunha, Araújo-Filho, Irami, de Oliveira, Anselmo Gomes [UNESP], do Egito, Eryvaldo Sócrates Tabosa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/226699
Resumo: The aim of this work was to evaluate how an aqueous micellar system containing Amphotericin B (AmB) and sodium deoxycholate (DOC) can be rebuilt after heating treatment. Also, a review of the literature on the physicochemical and biological properties of this new system was conducted. Heated (AmB-DOC-H) and unheated (AmB-DOC) micelles were then diluted at four different concentrations (50 mg. L -1, 5 mg. L -1, 0.5 mg. L -1, and 0.05 mg. L -1) to perform physicochemical studies and a pharmacotoxicity assay, in which two cell models were used for the in vitro experiments: red blood cells (RBC) from human donors and Candida parapsilosis (Cp). While potassium (K +) and hemoglobin leakage from RBC were the parameters used to evaluate acute and chronic toxicity, respectively, the effcacy of AmB-DOC and AmB-DOC-H were assessed by K + leakage and cell survival rate from Cp. The spectral study revealed a slight change in the AmB-DOC aggregate peak from 327 nm to 323 nm, which is the peak for AmB-DOC-H. Although AmB-DOC and AmB-DOC-H exhibited different behavior for hemoglobin leakage, AmB-DOC produced higher leakage than AmB-DOC-H at high concentrations (from 5 mg. L -1). For K + leakage, both AmB-DOC and AmB-DOC-H showed a similar profle for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profle of activity against Cp with an equivalent survival rate. In short, AmB-DOC-H showed much less toxicity than AmB-DOC, but remained as active as AmB-DOC against fungal cells. The results highlight the importance of this new procedure as a simple, inexpensive, and safe way to produce a new kind of micelle system for the treatment of systemic fungal infections. © 2012 Silva-Filho et al.
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spelling How can micelle systems be rebuilt by a heating process?MicellesNanotechnologyPre-heated amphotericin BSuper-aggregatesThe aim of this work was to evaluate how an aqueous micellar system containing Amphotericin B (AmB) and sodium deoxycholate (DOC) can be rebuilt after heating treatment. Also, a review of the literature on the physicochemical and biological properties of this new system was conducted. Heated (AmB-DOC-H) and unheated (AmB-DOC) micelles were then diluted at four different concentrations (50 mg. L -1, 5 mg. L -1, 0.5 mg. L -1, and 0.05 mg. L -1) to perform physicochemical studies and a pharmacotoxicity assay, in which two cell models were used for the in vitro experiments: red blood cells (RBC) from human donors and Candida parapsilosis (Cp). While potassium (K +) and hemoglobin leakage from RBC were the parameters used to evaluate acute and chronic toxicity, respectively, the effcacy of AmB-DOC and AmB-DOC-H were assessed by K + leakage and cell survival rate from Cp. The spectral study revealed a slight change in the AmB-DOC aggregate peak from 327 nm to 323 nm, which is the peak for AmB-DOC-H. Although AmB-DOC and AmB-DOC-H exhibited different behavior for hemoglobin leakage, AmB-DOC produced higher leakage than AmB-DOC-H at high concentrations (from 5 mg. L -1). For K + leakage, both AmB-DOC and AmB-DOC-H showed a similar profle for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profle of activity against Cp with an equivalent survival rate. In short, AmB-DOC-H showed much less toxicity than AmB-DOC, but remained as active as AmB-DOC against fungal cells. The results highlight the importance of this new procedure as a simple, inexpensive, and safe way to produce a new kind of micelle system for the treatment of systemic fungal infections. © 2012 Silva-Filho et al.Dispersed Systems Laboratory Federal University of rio grande do Norte (UFrN), Rio grande do Norte, 8948 NatalDepartment of Pharmacy UFrN, Natal, Rio grande do NorteDepartment of experimental Surgery UFrN, Natal, rio grande do NorteDepartment of Drugs and Medicines College of Pharmaceutical Sciences (UNeSP), Araraquara, São PauloDepartment of Drugs and Medicines College of Pharmaceutical Sciences (UNeSP), Araraquara, São PauloFederal University of rio grande do Norte (UFrN)UFrNUniversidade Estadual Paulista (UNESP)da Silva-Filho, Miguel AdelinoSiqueira, Scheyla Daniela Vieira da SilvaFreire, Larissa Bandeirade Araújo, Ivonete Batistade Holandae e Silva, Káttya Gyselleda Medeiros, Aldo CunhaAraújo-Filho, Iramide Oliveira, Anselmo Gomes [UNESP]do Egito, Eryvaldo Sócrates Tabosa2022-04-29T02:43:14Z2022-04-29T02:43:14Z2012-02-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article141-150International Journal of Nanomedicine, v. 7, p. 141-150.1176-91141178-2013http://hdl.handle.net/11449/2266992-s2.0-84856639968Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Nanomedicineinfo:eu-repo/semantics/openAccess2024-06-24T13:46:11Zoai:repositorio.unesp.br:11449/226699Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-06-24T13:46:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv How can micelle systems be rebuilt by a heating process?
title How can micelle systems be rebuilt by a heating process?
spellingShingle How can micelle systems be rebuilt by a heating process?
da Silva-Filho, Miguel Adelino
Micelles
Nanotechnology
Pre-heated amphotericin B
Super-aggregates
title_short How can micelle systems be rebuilt by a heating process?
title_full How can micelle systems be rebuilt by a heating process?
title_fullStr How can micelle systems be rebuilt by a heating process?
title_full_unstemmed How can micelle systems be rebuilt by a heating process?
title_sort How can micelle systems be rebuilt by a heating process?
author da Silva-Filho, Miguel Adelino
author_facet da Silva-Filho, Miguel Adelino
Siqueira, Scheyla Daniela Vieira da Silva
Freire, Larissa Bandeira
de Araújo, Ivonete Batista
de Holandae e Silva, Káttya Gyselle
da Medeiros, Aldo Cunha
Araújo-Filho, Irami
de Oliveira, Anselmo Gomes [UNESP]
do Egito, Eryvaldo Sócrates Tabosa
author_role author
author2 Siqueira, Scheyla Daniela Vieira da Silva
Freire, Larissa Bandeira
de Araújo, Ivonete Batista
de Holandae e Silva, Káttya Gyselle
da Medeiros, Aldo Cunha
Araújo-Filho, Irami
de Oliveira, Anselmo Gomes [UNESP]
do Egito, Eryvaldo Sócrates Tabosa
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of rio grande do Norte (UFrN)
UFrN
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv da Silva-Filho, Miguel Adelino
Siqueira, Scheyla Daniela Vieira da Silva
Freire, Larissa Bandeira
de Araújo, Ivonete Batista
de Holandae e Silva, Káttya Gyselle
da Medeiros, Aldo Cunha
Araújo-Filho, Irami
de Oliveira, Anselmo Gomes [UNESP]
do Egito, Eryvaldo Sócrates Tabosa
dc.subject.por.fl_str_mv Micelles
Nanotechnology
Pre-heated amphotericin B
Super-aggregates
topic Micelles
Nanotechnology
Pre-heated amphotericin B
Super-aggregates
description The aim of this work was to evaluate how an aqueous micellar system containing Amphotericin B (AmB) and sodium deoxycholate (DOC) can be rebuilt after heating treatment. Also, a review of the literature on the physicochemical and biological properties of this new system was conducted. Heated (AmB-DOC-H) and unheated (AmB-DOC) micelles were then diluted at four different concentrations (50 mg. L -1, 5 mg. L -1, 0.5 mg. L -1, and 0.05 mg. L -1) to perform physicochemical studies and a pharmacotoxicity assay, in which two cell models were used for the in vitro experiments: red blood cells (RBC) from human donors and Candida parapsilosis (Cp). While potassium (K +) and hemoglobin leakage from RBC were the parameters used to evaluate acute and chronic toxicity, respectively, the effcacy of AmB-DOC and AmB-DOC-H were assessed by K + leakage and cell survival rate from Cp. The spectral study revealed a slight change in the AmB-DOC aggregate peak from 327 nm to 323 nm, which is the peak for AmB-DOC-H. Although AmB-DOC and AmB-DOC-H exhibited different behavior for hemoglobin leakage, AmB-DOC produced higher leakage than AmB-DOC-H at high concentrations (from 5 mg. L -1). For K + leakage, both AmB-DOC and AmB-DOC-H showed a similar profle for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profle of activity against Cp with an equivalent survival rate. In short, AmB-DOC-H showed much less toxicity than AmB-DOC, but remained as active as AmB-DOC against fungal cells. The results highlight the importance of this new procedure as a simple, inexpensive, and safe way to produce a new kind of micelle system for the treatment of systemic fungal infections. © 2012 Silva-Filho et al.
publishDate 2012
dc.date.none.fl_str_mv 2012-02-10
2022-04-29T02:43:14Z
2022-04-29T02:43:14Z
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 International Journal of Nanomedicine, v. 7, p. 141-150.
1176-9114
1178-2013
http://hdl.handle.net/11449/226699
2-s2.0-84856639968
identifier_str_mv International Journal of Nanomedicine, v. 7, p. 141-150.
1176-9114
1178-2013
2-s2.0-84856639968
url http://hdl.handle.net/11449/226699
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Nanomedicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 141-150
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
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