In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis

Detalhes bibliográficos
Autor(a) principal: Agertt, Vanessa Albertina
Data de Publicação: 2016
Outros Autores: Bonez, Pauline Cordenonsi, Mizdal, Caren Rigon, Rossi, Grazielle Guidolin, Flores, Vanessa da Costa, Campos, Marli Matiko Anraku de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/128355
Resumo: The use of drugs in fixed-dose combination (FDC) is now recommended by the World Health Organization (WHO) due to the emergence of multidrug-resistant strains of Mycobacterium tuberculosis. FDC uses different drugs against tuberculosis (TB) in a single tablet for phase-intensive therapeutic intervention. This therapy aims to optimize treatment, to prevent inappropriate use of drugs, and to prevent the emergence of new resistant strains. This study aims to evaluate the susceptibility of clinical isolates of M. tuberculosis against rifampicin, isoniazid, ethambutol, and pyrazinamide. The antimicrobials were tested separately and in associations according to FDC. This was used for broth microdilution method, which was compared to the proportions method previously considered as the gold standard. In antimicrobials testing alone, several strains were resistant to one, two, or three drugs. However, when applied to association of drugs in FDC, there was no antimicrobial resistance. The results strengthen the FDC's concept, which aims to unite the four anti-TB drugs to combat bacterial resistance.
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spelling In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis The use of drugs in fixed-dose combination (FDC) is now recommended by the World Health Organization (WHO) due to the emergence of multidrug-resistant strains of Mycobacterium tuberculosis. FDC uses different drugs against tuberculosis (TB) in a single tablet for phase-intensive therapeutic intervention. This therapy aims to optimize treatment, to prevent inappropriate use of drugs, and to prevent the emergence of new resistant strains. This study aims to evaluate the susceptibility of clinical isolates of M. tuberculosis against rifampicin, isoniazid, ethambutol, and pyrazinamide. The antimicrobials were tested separately and in associations according to FDC. This was used for broth microdilution method, which was compared to the proportions method previously considered as the gold standard. In antimicrobials testing alone, several strains were resistant to one, two, or three drugs. However, when applied to association of drugs in FDC, there was no antimicrobial resistance. The results strengthen the FDC's concept, which aims to unite the four anti-TB drugs to combat bacterial resistance. Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2016-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/12835510.1590/s1984-82502016000300022Brazilian Journal of Pharmaceutical Sciences; Vol. 52 Núm. 3 (2016); 575-580Brazilian Journal of Pharmaceutical Sciences; v. 52 n. 3 (2016); 575-580Brazilian Journal of Pharmaceutical Sciences; Vol. 52 No. 3 (2016); 575-5802175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/128355/125227Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessAgertt, Vanessa AlbertinaBonez, Pauline CordenonsiMizdal, Caren RigonRossi, Grazielle GuidolinFlores, Vanessa da CostaCampos, Marli Matiko Anraku de2017-03-16T17:54:51Zoai:revistas.usp.br:article/128355Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2017-03-16T17:54:51Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
title In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
spellingShingle In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
Agertt, Vanessa Albertina
title_short In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
title_full In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
title_fullStr In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
title_full_unstemmed In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
title_sort In vitro antimicrobial efficacy of a fixed-dose combination of RHZE against M. tuberculosis
author Agertt, Vanessa Albertina
author_facet Agertt, Vanessa Albertina
Bonez, Pauline Cordenonsi
Mizdal, Caren Rigon
Rossi, Grazielle Guidolin
Flores, Vanessa da Costa
Campos, Marli Matiko Anraku de
author_role author
author2 Bonez, Pauline Cordenonsi
Mizdal, Caren Rigon
Rossi, Grazielle Guidolin
Flores, Vanessa da Costa
Campos, Marli Matiko Anraku de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Agertt, Vanessa Albertina
Bonez, Pauline Cordenonsi
Mizdal, Caren Rigon
Rossi, Grazielle Guidolin
Flores, Vanessa da Costa
Campos, Marli Matiko Anraku de
description The use of drugs in fixed-dose combination (FDC) is now recommended by the World Health Organization (WHO) due to the emergence of multidrug-resistant strains of Mycobacterium tuberculosis. FDC uses different drugs against tuberculosis (TB) in a single tablet for phase-intensive therapeutic intervention. This therapy aims to optimize treatment, to prevent inappropriate use of drugs, and to prevent the emergence of new resistant strains. This study aims to evaluate the susceptibility of clinical isolates of M. tuberculosis against rifampicin, isoniazid, ethambutol, and pyrazinamide. The antimicrobials were tested separately and in associations according to FDC. This was used for broth microdilution method, which was compared to the proportions method previously considered as the gold standard. In antimicrobials testing alone, several strains were resistant to one, two, or three drugs. However, when applied to association of drugs in FDC, there was no antimicrobial resistance. The results strengthen the FDC's concept, which aims to unite the four anti-TB drugs to combat bacterial resistance.
publishDate 2016
dc.date.none.fl_str_mv 2016-09-01
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/128355
10.1590/s1984-82502016000300022
url https://www.revistas.usp.br/bjps/article/view/128355
identifier_str_mv 10.1590/s1984-82502016000300022
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/128355/125227
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. 52 Núm. 3 (2016); 575-580
Brazilian Journal of Pharmaceutical Sciences; v. 52 n. 3 (2016); 575-580
Brazilian Journal of Pharmaceutical Sciences; Vol. 52 No. 3 (2016); 575-580
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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