Development of microparticles and microparticulated tablets containing piperine
Autor(a) principal: | |
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Data de Publicação: | 2023 |
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/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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Brazilian Journal of Pharmaceutical Sciences |
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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 |
_version_ |
1800222918067617792 |