Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/131422 |
Resumo: | Gastroretentive floating microparticles were developed and evaluated for the controlled metronidazole delivery for treatment of gastric disease. Floating microparticles, varying in proportions of chitosan and hydroxypropyl methylcellulose or ethylcellulose, were obtained by spray drying. Floating microparticles were characterized by physicochemical and in vitro studies, according to their floating ability and drug delivery. Microparticles presented mean diameter from 1.05 to 2.20 µm. The infrared spectroscopy confirmed the drug encapsulation and showed no chemical linkage between microparticles components. X-ray diffraction showed changes in the drug`s solid state, from crystalline to amorphous, indicating partial drug encapsulation, due to the presence of some crystalline peaks of metronidazole in microparticles. All microparticles floated immediately in contact of simulated gastric fluid and both floating and drug release profiles were dependent of microparticles composition. Microparticles samples constituted by chitosan and hydroxypropyl methylcellulose revealed the best relationship between floating duration and drug release, remaining floating during the occurrence of the drug release, ideal condition for the floating gastroretentive systems. |
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oai:revistas.usp.br:article/131422 |
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Brazilian Journal of Pharmaceutical Sciences |
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Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray dryingFloating microparticleChitosanEthylcelluloseHydroxypropyl methylcelluloseControlled drug delivery.Gastroretentive floating microparticles were developed and evaluated for the controlled metronidazole delivery for treatment of gastric disease. Floating microparticles, varying in proportions of chitosan and hydroxypropyl methylcellulose or ethylcellulose, were obtained by spray drying. Floating microparticles were characterized by physicochemical and in vitro studies, according to their floating ability and drug delivery. Microparticles presented mean diameter from 1.05 to 2.20 µm. The infrared spectroscopy confirmed the drug encapsulation and showed no chemical linkage between microparticles components. X-ray diffraction showed changes in the drug`s solid state, from crystalline to amorphous, indicating partial drug encapsulation, due to the presence of some crystalline peaks of metronidazole in microparticles. All microparticles floated immediately in contact of simulated gastric fluid and both floating and drug release profiles were dependent of microparticles composition. Microparticles samples constituted by chitosan and hydroxypropyl methylcellulose revealed the best relationship between floating duration and drug release, remaining floating during the occurrence of the drug release, ideal condition for the floating gastroretentive systems.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/13142210.1590/s2175-97902017000115218Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 1 (2017); e15218-Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 1 (2017); e15218-Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 1 (2017); e15218-2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/131422/127802Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessNohemann, LaísAlmeida, Marina Penteado deFerrari, Priscileila Colerato2017-04-20T20:28:50Zoai:revistas.usp.br:article/131422Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2017-04-20T20:28:50Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
title |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
spellingShingle |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying Nohemann, Laís Floating microparticle Chitosan Ethylcellulose Hydroxypropyl methylcellulose Controlled drug delivery. |
title_short |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
title_full |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
title_fullStr |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
title_full_unstemmed |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
title_sort |
Floating ability and drug release evaluation of gastroretentive microparticles system containing metronidazole obtained by spray drying |
author |
Nohemann, Laís |
author_facet |
Nohemann, Laís Almeida, Marina Penteado de Ferrari, Priscileila Colerato |
author_role |
author |
author2 |
Almeida, Marina Penteado de Ferrari, Priscileila Colerato |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Nohemann, Laís Almeida, Marina Penteado de Ferrari, Priscileila Colerato |
dc.subject.por.fl_str_mv |
Floating microparticle Chitosan Ethylcellulose Hydroxypropyl methylcellulose Controlled drug delivery. |
topic |
Floating microparticle Chitosan Ethylcellulose Hydroxypropyl methylcellulose Controlled drug delivery. |
description |
Gastroretentive floating microparticles were developed and evaluated for the controlled metronidazole delivery for treatment of gastric disease. Floating microparticles, varying in proportions of chitosan and hydroxypropyl methylcellulose or ethylcellulose, were obtained by spray drying. Floating microparticles were characterized by physicochemical and in vitro studies, according to their floating ability and drug delivery. Microparticles presented mean diameter from 1.05 to 2.20 µm. The infrared spectroscopy confirmed the drug encapsulation and showed no chemical linkage between microparticles components. X-ray diffraction showed changes in the drug`s solid state, from crystalline to amorphous, indicating partial drug encapsulation, due to the presence of some crystalline peaks of metronidazole in microparticles. All microparticles floated immediately in contact of simulated gastric fluid and both floating and drug release profiles were dependent of microparticles composition. Microparticles samples constituted by chitosan and hydroxypropyl methylcellulose revealed the best relationship between floating duration and drug release, remaining floating during the occurrence of the drug release, ideal condition for the floating gastroretentive systems. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/131422 10.1590/s2175-97902017000115218 |
url |
https://www.revistas.usp.br/bjps/article/view/131422 |
identifier_str_mv |
10.1590/s2175-97902017000115218 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/131422/127802 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 1 (2017); e15218- Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 1 (2017); e15218- Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 1 (2017); e15218- 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1800222912912818176 |