Development of microparticles and microparticulated tablets containing piperine

Detalhes bibliográficos
Autor(a) principal: Schneider, Aline Colling
Data de Publicação: 2023
Outros Autores: Brener, Carlos Eduardo de Souza, Daudt, Natália de Freitas, Cruz, Letícia, da Silva, Cristiane
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/211934
Resumo: Piper nigrum (black pepper) is used in Indian traditional medicine and its main alkaloid, Piperine (PIP), presents antioxidant, antitumor and neuroprotective pharmacological properties. This substance is insoluble in aqueous media and can irritate the gastrointestinal tract. Aiming to avoid these inconvenient characteristics and enable PIP oral administration, this study suggested the PIP microencapsulation through the emulsion-solvent evaporation method and the preparation of microparticulated tablets by direct compression. An UV-spectroscopy method was validated to quantify PIP. Microparticles and microparticulated tablets were successfully obtained and the microparticles exhibited excellent flow. The scanning electron microscopy images showed that PIP microparticles were intact after compression. The in vitro release showed a controlled release of PIP from microparticles and PIP microparticles from tablets in comparison to PIP and PIP tablets. The release profiles of PIP microparticles and the microparticulated tablets were similar. Therefore, tablets containing PIP microparticles are promising multiparticulated dosage forms because a tablet allows microparticles administration and the intact ones promote a controlled release, decreasing its irritating potential on the mucosa.
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spelling Development of microparticles and microparticulated tablets containing piperineEthylcellulose; Piper nigrum; Compression; Microencapsulation; Polacrilin potassiumPiper nigrum (black pepper) is used in Indian traditional medicine and its main alkaloid, Piperine (PIP), presents antioxidant, antitumor and neuroprotective pharmacological properties. This substance is insoluble in aqueous media and can irritate the gastrointestinal tract. Aiming to avoid these inconvenient characteristics and enable PIP oral administration, this study suggested the PIP microencapsulation through the emulsion-solvent evaporation method and the preparation of microparticulated tablets by direct compression. An UV-spectroscopy method was validated to quantify PIP. Microparticles and microparticulated tablets were successfully obtained and the microparticles exhibited excellent flow. The scanning electron microscopy images showed that PIP microparticles were intact after compression. The in vitro release showed a controlled release of PIP from microparticles and PIP microparticles from tablets in comparison to PIP and PIP tablets. The release profiles of PIP microparticles and the microparticulated tablets were similar. Therefore, tablets containing PIP microparticles are promising multiparticulated dosage forms because a tablet allows microparticles administration and the intact ones promote a controlled release, decreasing its irritating potential on the mucosa.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-05-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/21193410.1590/s2175-97902023e21265Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21265Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21265Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e212652175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/211934/194722https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessSchneider, Aline CollingBrener, Carlos Eduardo de SouzaDaudt, Natália de FreitasCruz, Letíciada Silva, Cristiane2023-06-02T21:39:22Zoai:revistas.usp.br:article/211934Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-06-02T21:39:22Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Development of microparticles and microparticulated tablets containing piperine
title Development of microparticles and microparticulated tablets containing piperine
spellingShingle Development of microparticles and microparticulated tablets containing piperine
Schneider, Aline Colling
Ethylcellulose; Piper nigrum; Compression; Microencapsulation; Polacrilin potassium
title_short Development of microparticles and microparticulated tablets containing piperine
title_full Development of microparticles and microparticulated tablets containing piperine
title_fullStr Development of microparticles and microparticulated tablets containing piperine
title_full_unstemmed Development of microparticles and microparticulated tablets containing piperine
title_sort Development of microparticles and microparticulated tablets containing piperine
author Schneider, Aline Colling
author_facet Schneider, Aline Colling
Brener, Carlos Eduardo de Souza
Daudt, Natália de Freitas
Cruz, Letícia
da Silva, Cristiane
author_role author
author2 Brener, Carlos Eduardo de Souza
Daudt, Natália de Freitas
Cruz, Letícia
da Silva, Cristiane
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Schneider, Aline Colling
Brener, Carlos Eduardo de Souza
Daudt, Natália de Freitas
Cruz, Letícia
da Silva, Cristiane
dc.subject.por.fl_str_mv Ethylcellulose; Piper nigrum; Compression; Microencapsulation; Polacrilin potassium
topic Ethylcellulose; Piper nigrum; Compression; Microencapsulation; Polacrilin potassium
description Piper nigrum (black pepper) is used in Indian traditional medicine and its main alkaloid, Piperine (PIP), presents antioxidant, antitumor and neuroprotective pharmacological properties. This substance is insoluble in aqueous media and can irritate the gastrointestinal tract. Aiming to avoid these inconvenient characteristics and enable PIP oral administration, this study suggested the PIP microencapsulation through the emulsion-solvent evaporation method and the preparation of microparticulated tablets by direct compression. An UV-spectroscopy method was validated to quantify PIP. Microparticles and microparticulated tablets were successfully obtained and the microparticles exhibited excellent flow. The scanning electron microscopy images showed that PIP microparticles were intact after compression. The in vitro release showed a controlled release of PIP from microparticles and PIP microparticles from tablets in comparison to PIP and PIP tablets. The release profiles of PIP microparticles and the microparticulated tablets were similar. Therefore, tablets containing PIP microparticles are promising multiparticulated dosage forms because a tablet allows microparticles administration and the intact ones promote a controlled release, decreasing its irritating potential on the mucosa.
publishDate 2023
dc.date.none.fl_str_mv 2023-05-08
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/211934
10.1590/s2175-97902023e21265
url https://www.revistas.usp.br/bjps/article/view/211934
identifier_str_mv 10.1590/s2175-97902023e21265
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/211934/194722
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
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. 59 (2023); e21265
Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21265
Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21265
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
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