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dc.contributor.author
Valenzuela Oses, Johanna K.  
dc.contributor.author
García, Mónica Cristina  
dc.contributor.author
Feitosa, Valker A.  
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Pachioni Vasconcelos, Juliana A.  
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Gomes-Filho, Sandro M.  
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Lourenço, Felipe R.  
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Cerize, Natalia N.P.  
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Bassères, Daniela S.  
dc.contributor.author
Rangel-Yagui, Carlota O.  
dc.date.available
2018-12-03T19:05:53Z  
dc.date.issued
2017-12  
dc.identifier.citation
Valenzuela Oses, Johanna K.; García, Mónica Cristina; Feitosa, Valker A.; Pachioni Vasconcelos, Juliana A.; Gomes-Filho, Sandro M.; et al.; Development and characterization of miltefosine-loaded polymeric micelles for cancer treatment; Elsevier Science; Materials Science and Engineering: C; 81; 12-2017; 327-333  
dc.identifier.issn
0928-4931  
dc.identifier.uri
http://hdl.handle.net/11336/65640  
dc.description.abstract
Miltefosine presents antineoplastic activity but high hemolytic potential. Its use in cancer has been limited to treating cutaneous metastasis of breast cancer. To decrease hemolytic potential, we developed a formulation of miltefosine-loaded polymeric micelles (PM) of the copolymer Pluronic-F127. A central composite design was applied and the analysis of variance showed that the optimum level of hydrodynamic diameter and polydispersity index predicted by the model and experimentally confirmed were 29 nm and 0.105, respectively. Thermal analyses confirmed that miltefosine was molecularly dispersed within PM. Pluronic-F127 PM with miltefosine 80 μM presented a significant reduction of hemolytic effect (80%, p < 0.05) in comparison to free drug. In vitro assays against HeLa carcinoma cells demonstrated similar cytotoxicity to free miltefosine and PM. Our results suggest that, by lowering hemolytic potential, miltefosine-loaded Pluronic-F127 PM a promising alternative to broaden this drug use in cancer therapy, as well as of other alkylphosphocholines.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Alkylphosphocholines  
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Block-Copolymer  
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Cancer Therapy  
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Hemolytic Potential  
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Miltefosine  
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Polymeric Micelles  
dc.subject.classification
Nano-materiales  
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Nanotecnología  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Development and characterization of miltefosine-loaded polymeric micelles for cancer treatment  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-10-22T19:36:26Z  
dc.journal.volume
81  
dc.journal.pagination
327-333  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Valenzuela Oses, Johanna K.. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: García, Mónica Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina  
dc.description.fil
Fil: Feitosa, Valker A.. Universidade de Sao Paulo; Brasil. Institute for Technological Research; Brasil  
dc.description.fil
Fil: Pachioni Vasconcelos, Juliana A.. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: Gomes-Filho, Sandro M.. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: Lourenço, Felipe R.. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: Cerize, Natalia N.P.. Institute for Technological Research; Brasil  
dc.description.fil
Fil: Bassères, Daniela S.. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: Rangel-Yagui, Carlota O.. Universidade de Sao Paulo; Brasil  
dc.journal.title
Materials Science and Engineering: C  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://linkinghub.elsevier.com/retrieve/pii/S0928493117320921  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.msec.2017.07.040