Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.xphs.2015.11.016 http://hdl.handle.net/11449/159040 |
Resumo: | The aim of the present work was to develop a topical delivery system that contains Brazilian green propolis extract (PE-8) to increase efficiency and convenience when applied to herpetic lesions. The cytotoxicity and antiherpetic activity was determined in vitro and in vivo. The PE-8 was added to a system that contained poloxamer 407 and carbopol 934P. The in vitro characterization of the system included rheological studies, texture profile analysis, and mucoadhesion analysis. The PE-8 inhibited the virus during the phase of viral infection, induced virion damage, and exhibited an ability to protect cells from viral infection. The system had advantageous mucoadhesive properties, including a suitable gelation temperature of approximately 25 degrees C for topical delivery, a desirable textural profile, and pseudoplastic behavior. The in vitro release study showed a rapid initial release of the PE-8 in the first 3 h, and the rate of drug release remained constant for up to 24 h. The system appeared to be macroscopically and microscopically innocuous to skin tissue. Therefore, the mucoadhesive thermoresponsive system that contained the PE-8 appears to be promising for increasing bioavailability and achieving prolonged release of the PE-8 when applied to skin lesions caused by herpes simplex virus type 1. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved. |
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Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type Iherpes simplex type IBrazilian green propolismucoadhesiveviscoelasticrheologyThe aim of the present work was to develop a topical delivery system that contains Brazilian green propolis extract (PE-8) to increase efficiency and convenience when applied to herpetic lesions. The cytotoxicity and antiherpetic activity was determined in vitro and in vivo. The PE-8 was added to a system that contained poloxamer 407 and carbopol 934P. The in vitro characterization of the system included rheological studies, texture profile analysis, and mucoadhesion analysis. The PE-8 inhibited the virus during the phase of viral infection, induced virion damage, and exhibited an ability to protect cells from viral infection. The system had advantageous mucoadhesive properties, including a suitable gelation temperature of approximately 25 degrees C for topical delivery, a desirable textural profile, and pseudoplastic behavior. The in vitro release study showed a rapid initial release of the PE-8 in the first 3 h, and the rate of drug release remained constant for up to 24 h. The system appeared to be macroscopically and microscopically innocuous to skin tissue. Therefore, the mucoadhesive thermoresponsive system that contained the PE-8 appears to be promising for increasing bioavailability and achieving prolonged release of the PE-8 when applied to skin lesions caused by herpes simplex virus type 1. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundacao AraucariaFINEPConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Estadual Maringa, Programa Posgrad Ciencias Farmaceut, Maringa, Parana, BrazilUniv Estadual Paulista, Programa Posgrad Ciencias Farmaceut, Fac Ciencias Farmaceut Araraquara, Sao Paulo, BrazilUniv Estadual Maringa, Dept Ciencias Morfol, Maringa, Parana, BrazilUniv Estadual Maringa, Dept Ciencias Basicas Saude, Maringa, Parana, BrazilUniv Estadual Maringa, Dept Farm, Maringa, Parana, BrazilUniv Estadual Paulista, Programa Posgrad Ciencias Farmaceut, Fac Ciencias Farmaceut Araraquara, Sao Paulo, BrazilWiley-BlackwellUniversidade Estadual de Maringá (UEM)Universidade Estadual Paulista (Unesp)Mazia, Renata SespedeAraujo Pereira, Raphaela Regina de [UNESP]Belloto de Francisco, Lizziane MariaMarcal Natali, Maria RaquelDias Filho, Benedito PradoNakamura, Celso VataruBruschi, Marcos LucianoUeda-Nakamura, Tania2018-11-26T15:31:03Z2018-11-26T15:31:03Z2016-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article113-121http://dx.doi.org/10.1016/j.xphs.2015.11.016Journal Of Pharmaceutical Sciences. Hoboken: Wiley-blackwell, v. 105, n. 1, p. 113-121, 2016.0022-3549http://hdl.handle.net/11449/15904010.1016/j.xphs.2015.11.016WOS:000381768000016Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Pharmaceutical Sciences0,984info:eu-repo/semantics/openAccess2021-10-23T16:22:42Zoai:repositorio.unesp.br:11449/159040Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:39:42.647493Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
title |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
spellingShingle |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I Mazia, Renata Sespede herpes simplex type I Brazilian green propolis mucoadhesive viscoelastic rheology |
title_short |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
title_full |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
title_fullStr |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
title_full_unstemmed |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
title_sort |
Formulation and Evaluation of a Mucoadhesive Thermoresponsive System Containing Brazilian Green Propolis for the Treatment of Lesions Caused by Herpes Simplex Type I |
author |
Mazia, Renata Sespede |
author_facet |
Mazia, Renata Sespede Araujo Pereira, Raphaela Regina de [UNESP] Belloto de Francisco, Lizziane Maria Marcal Natali, Maria Raquel Dias Filho, Benedito Prado Nakamura, Celso Vataru Bruschi, Marcos Luciano Ueda-Nakamura, Tania |
author_role |
author |
author2 |
Araujo Pereira, Raphaela Regina de [UNESP] Belloto de Francisco, Lizziane Maria Marcal Natali, Maria Raquel Dias Filho, Benedito Prado Nakamura, Celso Vataru Bruschi, Marcos Luciano Ueda-Nakamura, Tania |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Maringá (UEM) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Mazia, Renata Sespede Araujo Pereira, Raphaela Regina de [UNESP] Belloto de Francisco, Lizziane Maria Marcal Natali, Maria Raquel Dias Filho, Benedito Prado Nakamura, Celso Vataru Bruschi, Marcos Luciano Ueda-Nakamura, Tania |
dc.subject.por.fl_str_mv |
herpes simplex type I Brazilian green propolis mucoadhesive viscoelastic rheology |
topic |
herpes simplex type I Brazilian green propolis mucoadhesive viscoelastic rheology |
description |
The aim of the present work was to develop a topical delivery system that contains Brazilian green propolis extract (PE-8) to increase efficiency and convenience when applied to herpetic lesions. The cytotoxicity and antiherpetic activity was determined in vitro and in vivo. The PE-8 was added to a system that contained poloxamer 407 and carbopol 934P. The in vitro characterization of the system included rheological studies, texture profile analysis, and mucoadhesion analysis. The PE-8 inhibited the virus during the phase of viral infection, induced virion damage, and exhibited an ability to protect cells from viral infection. The system had advantageous mucoadhesive properties, including a suitable gelation temperature of approximately 25 degrees C for topical delivery, a desirable textural profile, and pseudoplastic behavior. The in vitro release study showed a rapid initial release of the PE-8 in the first 3 h, and the rate of drug release remained constant for up to 24 h. The system appeared to be macroscopically and microscopically innocuous to skin tissue. Therefore, the mucoadhesive thermoresponsive system that contained the PE-8 appears to be promising for increasing bioavailability and achieving prolonged release of the PE-8 when applied to skin lesions caused by herpes simplex virus type 1. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-01-01 2018-11-26T15:31:03Z 2018-11-26T15:31:03Z |
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/10.1016/j.xphs.2015.11.016 Journal Of Pharmaceutical Sciences. Hoboken: Wiley-blackwell, v. 105, n. 1, p. 113-121, 2016. 0022-3549 http://hdl.handle.net/11449/159040 10.1016/j.xphs.2015.11.016 WOS:000381768000016 |
url |
http://dx.doi.org/10.1016/j.xphs.2015.11.016 http://hdl.handle.net/11449/159040 |
identifier_str_mv |
Journal Of Pharmaceutical Sciences. Hoboken: Wiley-blackwell, v. 105, n. 1, p. 113-121, 2016. 0022-3549 10.1016/j.xphs.2015.11.016 WOS:000381768000016 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Pharmaceutical Sciences 0,984 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
113-121 |
dc.publisher.none.fl_str_mv |
Wiley-Blackwell |
publisher.none.fl_str_mv |
Wiley-Blackwell |
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 |
|
_version_ |
1808129448033124352 |