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: Vieira da Silva Siqueira, Scheyla Daniela, Freire, Larissa Bandeira, de Araujo, Ivonete Batista, Gyselle de Holanda e Silva, Kattya, Medeiros, Aldo da Cunha, Araujo-Filho, Irami, Oliveira, Anselmo Gomes de [UNESP], Tabosa do Egito, Eryvaldo Socrates
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.2147/IJN.S25761
http://hdl.handle.net/11449/7920
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 efficacy 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 profile for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profile 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.
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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 efficacy 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 profile for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profile 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.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fed Univ Rio Grande Norte UFRN, Dispersed Syst Lab, BR-59094450 Natal, RN, BrazilUniv Fed Rio Grande do Norte, Dept Pharm, Natal, RN, BrazilUniv Fed Rio Grande do Norte, Dept Expt Surg, Natal, RN, BrazilColl Pharmaceut Sci UNESP, Dept Drugs & Med, São Paulo, BrazilColl Pharmaceut Sci UNESP, Dept Drugs & Med, São Paulo, BrazilCNPq: 301979/04-9CNPq: 473882/04-3CNPq: 47836/01-7-NVDove Medical Press LtdUniversidade Federal do Rio Grande do Norte (UFRN)Universidade Estadual Paulista (Unesp)da Silva-Filho, Miguel AdelinoVieira da Silva Siqueira, Scheyla DanielaFreire, Larissa Bandeirade Araujo, Ivonete BatistaGyselle de Holanda e Silva, KattyaMedeiros, Aldo da CunhaAraujo-Filho, IramiOliveira, Anselmo Gomes de [UNESP]Tabosa do Egito, Eryvaldo Socrates2014-05-20T13:25:02Z2014-05-20T13:25:02Z2012-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article141-150application/pdfhttp://dx.doi.org/10.2147/IJN.S25761International Journal of Nanomedicine. Albany: Dove Medical Press Ltd, v. 7, p. 141-150, 2012.1178-2013http://hdl.handle.net/11449/792010.2147/IJN.S25761WOS:000302700700001WOS000302700700001.pdf9114495952533044Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Nanomedicine4.3701,225info:eu-repo/semantics/openAccess2024-06-24T13:45:30Zoai:repositorio.unesp.br:11449/7920Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-06-24T13:45:30Repositório 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
Vieira da Silva Siqueira, Scheyla Daniela
Freire, Larissa Bandeira
de Araujo, Ivonete Batista
Gyselle de Holanda e Silva, Kattya
Medeiros, Aldo da Cunha
Araujo-Filho, Irami
Oliveira, Anselmo Gomes de [UNESP]
Tabosa do Egito, Eryvaldo Socrates
author_role author
author2 Vieira da Silva Siqueira, Scheyla Daniela
Freire, Larissa Bandeira
de Araujo, Ivonete Batista
Gyselle de Holanda e Silva, Kattya
Medeiros, Aldo da Cunha
Araujo-Filho, Irami
Oliveira, Anselmo Gomes de [UNESP]
Tabosa do Egito, Eryvaldo Socrates
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Rio Grande do Norte (UFRN)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv da Silva-Filho, Miguel Adelino
Vieira da Silva Siqueira, Scheyla Daniela
Freire, Larissa Bandeira
de Araujo, Ivonete Batista
Gyselle de Holanda e Silva, Kattya
Medeiros, Aldo da Cunha
Araujo-Filho, Irami
Oliveira, Anselmo Gomes de [UNESP]
Tabosa do Egito, Eryvaldo Socrates
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 efficacy 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 profile for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profile 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.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
2014-05-20T13:25:02Z
2014-05-20T13:25:02Z
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/10.2147/IJN.S25761
International Journal of Nanomedicine. Albany: Dove Medical Press Ltd, v. 7, p. 141-150, 2012.
1178-2013
http://hdl.handle.net/11449/7920
10.2147/IJN.S25761
WOS:000302700700001
WOS000302700700001.pdf
9114495952533044
url http://dx.doi.org/10.2147/IJN.S25761
http://hdl.handle.net/11449/7920
identifier_str_mv International Journal of Nanomedicine. Albany: Dove Medical Press Ltd, v. 7, p. 141-150, 2012.
1178-2013
10.2147/IJN.S25761
WOS:000302700700001
WOS000302700700001.pdf
9114495952533044
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Nanomedicine
4.370
1,225
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 141-150
application/pdf
dc.publisher.none.fl_str_mv Dove Medical Press Ltd
publisher.none.fl_str_mv Dove Medical Press Ltd
dc.source.none.fl_str_mv Web of Science
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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