Development of innovative polymer-based matricial nanostructures for ritonavir oral administration

Bibliographic Details
Main Author: Giaretta, Moisele
Publication Date: 2019
Other Authors: Bianchin, Mariana Domingues, Kanis, Luiz Alberto, Contri, Renata Vidor, Külkamp-Guerreiro, Irene Clemes
Format: Article
Language: eng
Source: Repositório Institucional da UFRGS
Download full: http://hdl.handle.net/10183/195768
Summary: Ritonavir is used in the treatment of pediatric human immunodeficiency virus infection. The aim of this study was to develop and evaluate innovative polymer-based matricial nanostructures containing ritonavir for a sustained delivery. Two formulations were prepared by interfacial deposition of preformed polymers using Eudragit® RS100 in combination with Polycaprolactone triol 300 (NPR-300) or Polycaprolactone triol 900 (NPR-900). Ritonavir (1 mgmL-1) was incorporated in the formulations. NPR-300 showed a mean size of 559 nm, SPAN of 1.66, zeta potential of 5.9 mV, pH of 4.23, drug content of 73%, and stability under storage for 15 days. NPR-900 showed a mean size of 120 nm, SPAN of 0.83, zeta potential of 7.0 mV, pH of 4.2, drug content of 81%, and stability under storage for 60 days. The ritonavir content was 100% incorporated in both formulations. TEM images demonstrated spherical matricial structures. The ritonavir release in the simulated gastric medium was controlled by incorporation into the nanoparticles, especially into NPR-900. The formulations showed mucoadhesive properties, and the taste evaluation by an in vivo sensory panel indicated that particle size might influence taste perception since the formulation with the larger size of the nanoparticles (NPR-300) worsened the taste of the suspension. The NPR-900 was the most promising nanoparticle formulation for oral delivery of ritonavir.
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spelling Giaretta, MoiseleBianchin, Mariana DominguesKanis, Luiz AlbertoContri, Renata VidorKülkamp-Guerreiro, Irene Clemes2019-06-13T02:31:25Z20191687-4129http://hdl.handle.net/10183/195768001093554Ritonavir is used in the treatment of pediatric human immunodeficiency virus infection. The aim of this study was to develop and evaluate innovative polymer-based matricial nanostructures containing ritonavir for a sustained delivery. Two formulations were prepared by interfacial deposition of preformed polymers using Eudragit® RS100 in combination with Polycaprolactone triol 300 (NPR-300) or Polycaprolactone triol 900 (NPR-900). Ritonavir (1 mgmL-1) was incorporated in the formulations. NPR-300 showed a mean size of 559 nm, SPAN of 1.66, zeta potential of 5.9 mV, pH of 4.23, drug content of 73%, and stability under storage for 15 days. NPR-900 showed a mean size of 120 nm, SPAN of 0.83, zeta potential of 7.0 mV, pH of 4.2, drug content of 81%, and stability under storage for 60 days. The ritonavir content was 100% incorporated in both formulations. TEM images demonstrated spherical matricial structures. The ritonavir release in the simulated gastric medium was controlled by incorporation into the nanoparticles, especially into NPR-900. The formulations showed mucoadhesive properties, and the taste evaluation by an in vivo sensory panel indicated that particle size might influence taste perception since the formulation with the larger size of the nanoparticles (NPR-300) worsened the taste of the suspension. The NPR-900 was the most promising nanoparticle formulation for oral delivery of ritonavir.application/pdfengJournal of nanomaterials [recurso eletrônico]. New York. Vol. 2019 (2019), Article ID 8619819, 10 p.RitonavirNanoestruturasAdministração oralDevelopment of innovative polymer-based matricial nanostructures for ritonavir oral administrationEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001093554.pdf.txt001093554.pdf.txtExtracted Texttext/plain43740http://www.lume.ufrgs.br/bitstream/10183/195768/2/001093554.pdf.txta31e8fc8fd2641524faee31e434b1ca3MD52ORIGINAL001093554.pdfTexto completo (inglês)application/pdf2669189http://www.lume.ufrgs.br/bitstream/10183/195768/1/001093554.pdf5041fc007ce723cbfec8f86751758eccMD5110183/1957682019-06-14 02:31:32.020876oai:www.lume.ufrgs.br:10183/195768Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2019-06-14T05:31:32Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
title Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
spellingShingle Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
Giaretta, Moisele
Ritonavir
Nanoestruturas
Administração oral
title_short Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
title_full Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
title_fullStr Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
title_full_unstemmed Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
title_sort Development of innovative polymer-based matricial nanostructures for ritonavir oral administration
author Giaretta, Moisele
author_facet Giaretta, Moisele
Bianchin, Mariana Domingues
Kanis, Luiz Alberto
Contri, Renata Vidor
Külkamp-Guerreiro, Irene Clemes
author_role author
author2 Bianchin, Mariana Domingues
Kanis, Luiz Alberto
Contri, Renata Vidor
Külkamp-Guerreiro, Irene Clemes
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Giaretta, Moisele
Bianchin, Mariana Domingues
Kanis, Luiz Alberto
Contri, Renata Vidor
Külkamp-Guerreiro, Irene Clemes
dc.subject.por.fl_str_mv Ritonavir
Nanoestruturas
Administração oral
topic Ritonavir
Nanoestruturas
Administração oral
description Ritonavir is used in the treatment of pediatric human immunodeficiency virus infection. The aim of this study was to develop and evaluate innovative polymer-based matricial nanostructures containing ritonavir for a sustained delivery. Two formulations were prepared by interfacial deposition of preformed polymers using Eudragit® RS100 in combination with Polycaprolactone triol 300 (NPR-300) or Polycaprolactone triol 900 (NPR-900). Ritonavir (1 mgmL-1) was incorporated in the formulations. NPR-300 showed a mean size of 559 nm, SPAN of 1.66, zeta potential of 5.9 mV, pH of 4.23, drug content of 73%, and stability under storage for 15 days. NPR-900 showed a mean size of 120 nm, SPAN of 0.83, zeta potential of 7.0 mV, pH of 4.2, drug content of 81%, and stability under storage for 60 days. The ritonavir content was 100% incorporated in both formulations. TEM images demonstrated spherical matricial structures. The ritonavir release in the simulated gastric medium was controlled by incorporation into the nanoparticles, especially into NPR-900. The formulations showed mucoadhesive properties, and the taste evaluation by an in vivo sensory panel indicated that particle size might influence taste perception since the formulation with the larger size of the nanoparticles (NPR-300) worsened the taste of the suspension. The NPR-900 was the most promising nanoparticle formulation for oral delivery of ritonavir.
publishDate 2019
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dc.relation.ispartof.pt_BR.fl_str_mv Journal of nanomaterials [recurso eletrônico]. New York. Vol. 2019 (2019), Article ID 8619819, 10 p.
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