The importance of toxicity tests for development and phytotherapy registration

Detalhes bibliográficos
Autor(a) principal: Silva, Maísa Gomes da
Data de Publicação: 2021
Outros Autores: Furtado, Mariely Mendes, Osório, Altamiro Teixeira, Morais, Ilmara Cecília Pinheiro da Silva, Amaral, Maurício Pires Moura do, Coêlho, Angélica Gomes, Arcanjo, Daniel Dias Rufino
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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spelling 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
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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
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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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