The importance of toxicity tests for development and phytotherapy registration
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/20137 |
Resumo: | Non-clinical toxicological studies work as a foundation in the process of developing new drugs, as they anticipate risks and, therefore, reduce the probability of a new drug interfering with cellular metabolism, harming the health of the individual, in addition to not fulfilling its pharmacological function in the body. Thus, considering the therapeutic potential of medicinal plants, this paper aims to describe the importance of toxicological tests and current aspects concerning the registration of herbal medicines in Brazil. In order to carry out this work, scientific databases were searched, such as: Periódicos CAPES and Scielo, and the database was complemented with articles from Brazilian legislation. There was no search restriction regarding the language and year of publication of the scientific materials, but rather regarding the relevance of their content for this article. Thus, it was observed that the regulatory role of ANVISA is essential to prevent ineffective, toxic and poor quality drugs from reaching the market and causing problems such as intoxication, interactions with other drugs, therapeutic damage, or even death. Thus, as it is a traditional health practice and has already been revealed in several studies as being of therapeutic utility by a significant portion of the population, it is interesting to discuss the current situation of herbal medicines and the seriousness that should be taken in their development, especially in light of the trials non-clinical toxicologicals as they can prevent public health problems in the short and long term. |
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The importance of toxicity tests for development and phytotherapy registrationLa importancia de las pruebas de toxicidad para el desarrollo y registro de medicina herbaria en BrasilA importância dos ensaios de toxicidade para o desenvolvimento e o registro de fitoterápicos no BrasilPhytotherapeutic DrugsLegislationToxicology.Medicamentos fitoterápicosLegislaciónToxicología.Medicamentos FitoterápicosLegislaçãoToxicologia.Non-clinical toxicological studies work as a foundation in the process of developing new drugs, as they anticipate risks and, therefore, reduce the probability of a new drug interfering with cellular metabolism, harming the health of the individual, in addition to not fulfilling its pharmacological function in the body. Thus, considering the therapeutic potential of medicinal plants, this paper aims to describe the importance of toxicological tests and current aspects concerning the registration of herbal medicines in Brazil. In order to carry out this work, scientific databases were searched, such as: Periódicos CAPES and Scielo, and the database was complemented with articles from Brazilian legislation. There was no search restriction regarding the language and year of publication of the scientific materials, but rather regarding the relevance of their content for this article. Thus, it was observed that the regulatory role of ANVISA is essential to prevent ineffective, toxic and poor quality drugs from reaching the market and causing problems such as intoxication, interactions with other drugs, therapeutic damage, or even death. Thus, as it is a traditional health practice and has already been revealed in several studies as being of therapeutic utility by a significant portion of the population, it is interesting to discuss the current situation of herbal medicines and the seriousness that should be taken in their development, especially in light of the trials non-clinical toxicologicals as they can prevent public health problems in the short and long term.Los estudios toxicológicos no clínicos funcionan como base en el proceso de desarrollo de nuevos fármacos, ya que anticipan riesgos y, por tanto, reducen la probabilidad de que un nuevo fármaco interfiera con el metabolismo celular, perjudicando la salud del individuo, además de no cumplir con su función. función farmacológica en el cuerpo. Así, considerando el potencial terapéutico de las plantas medicinales, este trabajo tiene como objetivo describir la importancia de las pruebas toxicológicas y los aspectos actuales relacionados con el registro de medicinas a base de hierbas en Brasil. Para la realización de este trabajo se realizaron búsquedas en bases de datos científicas, tales como: Periódicos CAPES y Scielo, y se complementó la base de datos con artículos de la legislación brasileña. No hubo restricción de búsqueda con respecto al idioma y año de publicación de los materiales científicos, sino más bien con respecto a la relevancia de su contenido para este artículo. Así, se observó que el rol regulador de ANVISA es fundamental para evitar que medicamentos ineficaces, tóxicos y de mala calidad lleguen al mercado y causen problemas como intoxicación, interacciones con otros medicamentos, daño terapéutico o incluso la muerte. Así, como es una práctica de salud tradicional y ya ha sido revelada en varios estudios como de utilidad terapéutica por una parte importante de la población, es interesante discutir la situación actual de las medicinas a base de hierbas y la seriedad que se debe tomar en su tratamiento. desarrollo, especialmente a la luz de los ensayos toxicológicos no clínicos ya que pueden prevenir problemas de salud pública a corto y largo plazo.Os estudos toxicológicos não-clínicos funcionam com um alicerce no processo de desenvolvimento de novos fármacos, visto que antecipam riscos e, portanto, reduzem a probabilidade de um novo fármaco interferir no metabolismo celular prejudicando a saúde do indivíduo além de não cumprir sua função farmacológica no organismo. Assim, considerando o potencial terapêutico das plantas medicinais, o presente trabalho tem como objetivo descrever a importância dos ensaios toxicológicos e os aspectos atuais concernentes ao registro de medicamentos fitoterápicos no Brasil. Para realização deste trabalho foram pesquisadas bases de dados científicas, tais como: Periódicos CAPES e Scielo, tendo o banco de dados sido complementado com artigos da legislação brasileira. Não houve restrição de busca quanto ao idioma ao ano de publicação dos materiais científicos, mas sim, quanto à relevância do seu conteúdo para o presente artigo. Dessa forma, observou-se que o papel regulador da ANVISA é fundamental para evitar que medicamentos ineficazes, tóxicos e de má qualidade alcancem o mercado e ocasionem problemas como intoxicações, interações com outros medicamentos, danos terapêuticos, ou até mesmo óbitos. Assim, por ser uma prática tradicional de saúde e já revelada em diversos estudos como de utilidade terapêutica por uma parcela significativa da população, torna-se interessante discutir a situação atual dos fitoterápicos e a seriedade que se deve ter no seu desenvolvimento principalmente diante dos ensaios toxicológicos não-clínicos uma vez que eles podem evitar problemas de saúde pública a curto e longo prazo.Research, Society and Development2021-09-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2013710.33448/rsd-v10i12.20137Research, Society and Development; Vol. 10 No. 12; e538101220137Research, Society and Development; Vol. 10 Núm. 12; e538101220137Research, Society and Development; v. 10 n. 12; e5381012201372525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/20137/18520Copyright (c) 2021 Maísa Gomes da Silva; Mariely Mendes Furtado; Altamiro Teixeira Osório; Ilmara Cecília Pinheiro da Silva Morais; Maurício Pires Moura do Amaral; Angélica Gomes Coêlho; Daniel Dias Rufino Arcanjohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSilva, Maísa Gomes da Furtado, Mariely MendesOsório, Altamiro Teixeira Morais, Ilmara Cecília Pinheiro da Silva Amaral, Maurício Pires Moura do Coêlho, Angélica Gomes Arcanjo, Daniel Dias Rufino 2021-11-14T20:26:51Zoai:ojs.pkp.sfu.ca:article/20137Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:39:52.482709Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
The importance of toxicity tests for development and phytotherapy registration La importancia de las pruebas de toxicidad para el desarrollo y registro de medicina herbaria en Brasil A importância dos ensaios de toxicidade para o desenvolvimento e o registro de fitoterápicos no Brasil |
title |
The importance of toxicity tests for development and phytotherapy registration |
spellingShingle |
The importance of toxicity tests for development and phytotherapy registration Silva, Maísa Gomes da Phytotherapeutic Drugs Legislation Toxicology. Medicamentos fitoterápicos Legislación Toxicología. Medicamentos Fitoterápicos Legislação Toxicologia. |
title_short |
The importance of toxicity tests for development and phytotherapy registration |
title_full |
The importance of toxicity tests for development and phytotherapy registration |
title_fullStr |
The importance of toxicity tests for development and phytotherapy registration |
title_full_unstemmed |
The importance of toxicity tests for development and phytotherapy registration |
title_sort |
The importance of toxicity tests for development and phytotherapy registration |
author |
Silva, Maísa Gomes da |
author_facet |
Silva, Maísa Gomes da Furtado, Mariely Mendes Osório, Altamiro Teixeira Morais, Ilmara Cecília Pinheiro da Silva Amaral, Maurício Pires Moura do Coêlho, Angélica Gomes Arcanjo, Daniel Dias Rufino |
author_role |
author |
author2 |
Furtado, Mariely Mendes Osório, Altamiro Teixeira Morais, Ilmara Cecília Pinheiro da Silva Amaral, Maurício Pires Moura do Coêlho, Angélica Gomes Arcanjo, Daniel Dias Rufino |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Silva, Maísa Gomes da Furtado, Mariely Mendes Osório, Altamiro Teixeira Morais, Ilmara Cecília Pinheiro da Silva Amaral, Maurício Pires Moura do Coêlho, Angélica Gomes Arcanjo, Daniel Dias Rufino |
dc.subject.por.fl_str_mv |
Phytotherapeutic Drugs Legislation Toxicology. Medicamentos fitoterápicos Legislación Toxicología. Medicamentos Fitoterápicos Legislação Toxicologia. |
topic |
Phytotherapeutic Drugs Legislation Toxicology. Medicamentos fitoterápicos Legislación Toxicología. Medicamentos Fitoterápicos Legislação Toxicologia. |
description |
Non-clinical toxicological studies work as a foundation in the process of developing new drugs, as they anticipate risks and, therefore, reduce the probability of a new drug interfering with cellular metabolism, harming the health of the individual, in addition to not fulfilling its pharmacological function in the body. Thus, considering the therapeutic potential of medicinal plants, this paper aims to describe the importance of toxicological tests and current aspects concerning the registration of herbal medicines in Brazil. In order to carry out this work, scientific databases were searched, such as: Periódicos CAPES and Scielo, and the database was complemented with articles from Brazilian legislation. There was no search restriction regarding the language and year of publication of the scientific materials, but rather regarding the relevance of their content for this article. Thus, it was observed that the regulatory role of ANVISA is essential to prevent ineffective, toxic and poor quality drugs from reaching the market and causing problems such as intoxication, interactions with other drugs, therapeutic damage, or even death. Thus, as it is a traditional health practice and has already been revealed in several studies as being of therapeutic utility by a significant portion of the population, it is interesting to discuss the current situation of herbal medicines and the seriousness that should be taken in their development, especially in light of the trials non-clinical toxicologicals as they can prevent public health problems in the short and long term. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-09-30 |
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://rsdjournal.org/index.php/rsd/article/view/20137 10.33448/rsd-v10i12.20137 |
url |
https://rsdjournal.org/index.php/rsd/article/view/20137 |
identifier_str_mv |
10.33448/rsd-v10i12.20137 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/20137/18520 |
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 |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 10 No. 12; e538101220137 Research, Society and Development; Vol. 10 Núm. 12; e538101220137 Research, Society and Development; v. 10 n. 12; e538101220137 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052788997357568 |