Increased body exposure to new anti-trypanosomal through nanoencapsulation.

Detalhes bibliográficos
Autor(a) principal: Branquinho, Renata Tupinambá
Data de Publicação: 2017
Outros Autores: Lana, Gwenaelle Elza Nathalie Pound, Milagre, Matheus Marques, Guimarães, Dênia Antunes Saúde, Vilela, José Mário Carneiro, Andrade, Margareth Spangler, Lana, Marta de, Mosqueira, Vanessa Carla Furtado
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFOP
Texto Completo: http://www.repositorio.ufop.br/handle/123456789/11016
Resumo: Lychnopholide, a lipophilic sesquiterpene lactone, is efficacious in mice at the acute and chronic phases of Chagas disease. Conventional poly-ε-caprolactone (PCL) and long-circulating poly(D,L-lactide)-block-polyethylene glycol (PLA-PEG) nanocapsules containing lychnopholide were developed and characterized. Lychnopholide presented high association efficiency (>90%) with the nanocapsules. A new, fast and simple HPLC-UV-based bioanalytical method was developed, validated in mouse plasma and applied to lychnopholide quantification in in vitro release kinetics and pharmacokinetics. The nanocapsules had mean hydrodynamic diameters in the range of 100–250 nm, negative zeta potentials (−30 mV to −57 mV), with good physical stability under storage. Atomic force microscopy morphological analysis revealed spherical monodispersed particles and the absence of lychnopholide crystallization or aggregation. Association of lychnopholide to PLA-PEG nanocapsules resulted in a 16-fold increase in body exposure, a 26-fold increase in plasma half-life and a dramatic reduction of the lychnopholide plasma clearance (17-fold) in comparison with free lychnopholide. The improved pharmacokinetic profile of lychnopholide in long-circulating nanocapsules is in agreement with the previously reported improved efficacy observed in Trypanosoma cruzi-infected mice. The present lychnopholide intravenous dosage form showed great potential for further pre-clinical and clinical studies in Chagas disease and cancer therapies.
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spelling Branquinho, Renata TupinambáLana, Gwenaelle Elza Nathalie PoundMilagre, Matheus MarquesGuimarães, Dênia Antunes SaúdeVilela, José Mário CarneiroAndrade, Margareth SpanglerLana, Marta deMosqueira, Vanessa Carla Furtado2019-04-15T14:34:15Z2019-04-15T14:34:15Z2017BRANQUINHO, R. T. et al. Increased body exposure to new anti-trypanosomal through nanoencapsulation. Scientific Reports, v. 7, p. 1-12, 2017. Disponível em: <https://www.nature.com/articles/s41598-017-08469-x>. Acesso em: 25 fev. 2019.20452322http://www.repositorio.ufop.br/handle/123456789/11016Lychnopholide, a lipophilic sesquiterpene lactone, is efficacious in mice at the acute and chronic phases of Chagas disease. Conventional poly-ε-caprolactone (PCL) and long-circulating poly(D,L-lactide)-block-polyethylene glycol (PLA-PEG) nanocapsules containing lychnopholide were developed and characterized. Lychnopholide presented high association efficiency (>90%) with the nanocapsules. A new, fast and simple HPLC-UV-based bioanalytical method was developed, validated in mouse plasma and applied to lychnopholide quantification in in vitro release kinetics and pharmacokinetics. The nanocapsules had mean hydrodynamic diameters in the range of 100–250 nm, negative zeta potentials (−30 mV to −57 mV), with good physical stability under storage. Atomic force microscopy morphological analysis revealed spherical monodispersed particles and the absence of lychnopholide crystallization or aggregation. Association of lychnopholide to PLA-PEG nanocapsules resulted in a 16-fold increase in body exposure, a 26-fold increase in plasma half-life and a dramatic reduction of the lychnopholide plasma clearance (17-fold) in comparison with free lychnopholide. The improved pharmacokinetic profile of lychnopholide in long-circulating nanocapsules is in agreement with the previously reported improved efficacy observed in Trypanosoma cruzi-infected mice. The present lychnopholide intravenous dosage form showed great potential for further pre-clinical and clinical studies in Chagas disease and cancer therapies.This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Fonte: o próprio artigoinfo:eu-repo/semantics/openAccessIncreased body exposure to new anti-trypanosomal through nanoencapsulation.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOPLICENSElicense.txtlicense.txttext/plain; charset=utf-8924http://www.repositorio.ufop.br/bitstream/123456789/11016/2/license.txt62604f8d955274beb56c80ce1ee5dcaeMD52ORIGINALARTIGO_IncreasedBodyExposure.pdfARTIGO_IncreasedBodyExposure.pdfapplication/pdf2161439http://www.repositorio.ufop.br/bitstream/123456789/11016/1/ARTIGO_IncreasedBodyExposure.pdf35dc82a375825ca21ac712f1355b41eaMD51123456789/110162019-04-15 10:34:15.122oai:localhost: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ório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332019-04-15T14:34:15Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false
dc.title.pt_BR.fl_str_mv Increased body exposure to new anti-trypanosomal through nanoencapsulation.
title Increased body exposure to new anti-trypanosomal through nanoencapsulation.
spellingShingle Increased body exposure to new anti-trypanosomal through nanoencapsulation.
Branquinho, Renata Tupinambá
title_short Increased body exposure to new anti-trypanosomal through nanoencapsulation.
title_full Increased body exposure to new anti-trypanosomal through nanoencapsulation.
title_fullStr Increased body exposure to new anti-trypanosomal through nanoencapsulation.
title_full_unstemmed Increased body exposure to new anti-trypanosomal through nanoencapsulation.
title_sort Increased body exposure to new anti-trypanosomal through nanoencapsulation.
author Branquinho, Renata Tupinambá
author_facet Branquinho, Renata Tupinambá
Lana, Gwenaelle Elza Nathalie Pound
Milagre, Matheus Marques
Guimarães, Dênia Antunes Saúde
Vilela, José Mário Carneiro
Andrade, Margareth Spangler
Lana, Marta de
Mosqueira, Vanessa Carla Furtado
author_role author
author2 Lana, Gwenaelle Elza Nathalie Pound
Milagre, Matheus Marques
Guimarães, Dênia Antunes Saúde
Vilela, José Mário Carneiro
Andrade, Margareth Spangler
Lana, Marta de
Mosqueira, Vanessa Carla Furtado
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Branquinho, Renata Tupinambá
Lana, Gwenaelle Elza Nathalie Pound
Milagre, Matheus Marques
Guimarães, Dênia Antunes Saúde
Vilela, José Mário Carneiro
Andrade, Margareth Spangler
Lana, Marta de
Mosqueira, Vanessa Carla Furtado
description Lychnopholide, a lipophilic sesquiterpene lactone, is efficacious in mice at the acute and chronic phases of Chagas disease. Conventional poly-ε-caprolactone (PCL) and long-circulating poly(D,L-lactide)-block-polyethylene glycol (PLA-PEG) nanocapsules containing lychnopholide were developed and characterized. Lychnopholide presented high association efficiency (>90%) with the nanocapsules. A new, fast and simple HPLC-UV-based bioanalytical method was developed, validated in mouse plasma and applied to lychnopholide quantification in in vitro release kinetics and pharmacokinetics. The nanocapsules had mean hydrodynamic diameters in the range of 100–250 nm, negative zeta potentials (−30 mV to −57 mV), with good physical stability under storage. Atomic force microscopy morphological analysis revealed spherical monodispersed particles and the absence of lychnopholide crystallization or aggregation. Association of lychnopholide to PLA-PEG nanocapsules resulted in a 16-fold increase in body exposure, a 26-fold increase in plasma half-life and a dramatic reduction of the lychnopholide plasma clearance (17-fold) in comparison with free lychnopholide. The improved pharmacokinetic profile of lychnopholide in long-circulating nanocapsules is in agreement with the previously reported improved efficacy observed in Trypanosoma cruzi-infected mice. The present lychnopholide intravenous dosage form showed great potential for further pre-clinical and clinical studies in Chagas disease and cancer therapies.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2019-04-15T14:34:15Z
dc.date.available.fl_str_mv 2019-04-15T14:34:15Z
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dc.identifier.citation.fl_str_mv BRANQUINHO, R. T. et al. Increased body exposure to new anti-trypanosomal through nanoencapsulation. Scientific Reports, v. 7, p. 1-12, 2017. Disponível em: <https://www.nature.com/articles/s41598-017-08469-x>. Acesso em: 25 fev. 2019.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufop.br/handle/123456789/11016
dc.identifier.issn.none.fl_str_mv 20452322
identifier_str_mv BRANQUINHO, R. T. et al. Increased body exposure to new anti-trypanosomal through nanoencapsulation. Scientific Reports, v. 7, p. 1-12, 2017. Disponível em: <https://www.nature.com/articles/s41598-017-08469-x>. Acesso em: 25 fev. 2019.
20452322
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