Triterpene derivatives as relevant scaffold for new antibiofilm drugs

Detalhes bibliográficos
Autor(a) principal: Silva, Gloria Narjara Santos da
Data de Publicação: 2019
Outros Autores: Barros, Muriel Primon de, Macedo, Alexandre José, Gnoatto, Simone Cristina Baggio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/231525
Resumo: New medicines for the treatment of bacterial biofilm formation are required. For this reason, this study shows the in vitro activity of betulinic acid (BA), ursolic acid (UA) and their twenty derivatives against planktonic and biofilmcells (gram-positive bacterial pathogens: Enterococcus faecalis, Staphylococcus aureus and Staphylococcus epidermidis). We evaluated the antibiofilmactivity (through the crystal violet method), as well as the antibacterial activity via absorbance (OD600) at concentrations of 5, 25 and 100 M. Likewise, the cytotoxicity of all compoundswas evaluated on a kidney African greenmonkey (VERO) cell line at the same concentration, byMTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) methodology. We verified for the first time whether different groups at carbon 3 (C-3) of triterpenes may interfere in the antibiofilm activity with minimal or no antibacterial effect. After the screening of 22 compounds at three distinct concentrations, we found antibiofilm activity for eight distinct derivatives without antibiotic effect. In particular, the derivative 2f, with an isopentanoyl ester at position C-3, was an antibiofilm activity against S. aureus without any effect upon mammalian cells.
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spelling Silva, Gloria Narjara Santos daBarros, Muriel Primon deMacedo, Alexandre JoséGnoatto, Simone Cristina Baggio2021-11-04T04:24:07Z20192218-273Xhttp://hdl.handle.net/10183/231525001121879New medicines for the treatment of bacterial biofilm formation are required. For this reason, this study shows the in vitro activity of betulinic acid (BA), ursolic acid (UA) and their twenty derivatives against planktonic and biofilmcells (gram-positive bacterial pathogens: Enterococcus faecalis, Staphylococcus aureus and Staphylococcus epidermidis). We evaluated the antibiofilmactivity (through the crystal violet method), as well as the antibacterial activity via absorbance (OD600) at concentrations of 5, 25 and 100 M. Likewise, the cytotoxicity of all compoundswas evaluated on a kidney African greenmonkey (VERO) cell line at the same concentration, byMTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) methodology. We verified for the first time whether different groups at carbon 3 (C-3) of triterpenes may interfere in the antibiofilm activity with minimal or no antibacterial effect. After the screening of 22 compounds at three distinct concentrations, we found antibiofilm activity for eight distinct derivatives without antibiotic effect. In particular, the derivative 2f, with an isopentanoyl ester at position C-3, was an antibiofilm activity against S. aureus without any effect upon mammalian cells.application/pdfengBiomolecules. Basel. Vol. 9. no. 2 (2019), 58, 11 p.BiofilmesAntibacterianosFarmáciaUrsolic acidBetulinic acidCytotoxicityPathogenic biofilmsBacterial pathogensTriterpene derivatives as relevant scaffold for new antibiofilm drugsEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001121879.pdf.txt001121879.pdf.txtExtracted Texttext/plain37750http://www.lume.ufrgs.br/bitstream/10183/231525/2/001121879.pdf.txt3f9749b608629840ba0094517ff2446fMD52ORIGINAL001121879.pdfTexto completo (inglês)application/pdf1291563http://www.lume.ufrgs.br/bitstream/10183/231525/1/001121879.pdf01382a86a5f11b693f05119aea8046a4MD5110183/2315252021-11-20 05:57:53.770793oai:www.lume.ufrgs.br:10183/231525Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-11-20T07:57:53Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Triterpene derivatives as relevant scaffold for new antibiofilm drugs
title Triterpene derivatives as relevant scaffold for new antibiofilm drugs
spellingShingle Triterpene derivatives as relevant scaffold for new antibiofilm drugs
Silva, Gloria Narjara Santos da
Biofilmes
Antibacterianos
Farmácia
Ursolic acid
Betulinic acid
Cytotoxicity
Pathogenic biofilms
Bacterial pathogens
title_short Triterpene derivatives as relevant scaffold for new antibiofilm drugs
title_full Triterpene derivatives as relevant scaffold for new antibiofilm drugs
title_fullStr Triterpene derivatives as relevant scaffold for new antibiofilm drugs
title_full_unstemmed Triterpene derivatives as relevant scaffold for new antibiofilm drugs
title_sort Triterpene derivatives as relevant scaffold for new antibiofilm drugs
author Silva, Gloria Narjara Santos da
author_facet Silva, Gloria Narjara Santos da
Barros, Muriel Primon de
Macedo, Alexandre José
Gnoatto, Simone Cristina Baggio
author_role author
author2 Barros, Muriel Primon de
Macedo, Alexandre José
Gnoatto, Simone Cristina Baggio
author2_role author
author
author
dc.contributor.author.fl_str_mv Silva, Gloria Narjara Santos da
Barros, Muriel Primon de
Macedo, Alexandre José
Gnoatto, Simone Cristina Baggio
dc.subject.por.fl_str_mv Biofilmes
Antibacterianos
Farmácia
topic Biofilmes
Antibacterianos
Farmácia
Ursolic acid
Betulinic acid
Cytotoxicity
Pathogenic biofilms
Bacterial pathogens
dc.subject.eng.fl_str_mv Ursolic acid
Betulinic acid
Cytotoxicity
Pathogenic biofilms
Bacterial pathogens
description New medicines for the treatment of bacterial biofilm formation are required. For this reason, this study shows the in vitro activity of betulinic acid (BA), ursolic acid (UA) and their twenty derivatives against planktonic and biofilmcells (gram-positive bacterial pathogens: Enterococcus faecalis, Staphylococcus aureus and Staphylococcus epidermidis). We evaluated the antibiofilmactivity (through the crystal violet method), as well as the antibacterial activity via absorbance (OD600) at concentrations of 5, 25 and 100 M. Likewise, the cytotoxicity of all compoundswas evaluated on a kidney African greenmonkey (VERO) cell line at the same concentration, byMTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) methodology. We verified for the first time whether different groups at carbon 3 (C-3) of triterpenes may interfere in the antibiofilm activity with minimal or no antibacterial effect. After the screening of 22 compounds at three distinct concentrations, we found antibiofilm activity for eight distinct derivatives without antibiotic effect. In particular, the derivative 2f, with an isopentanoyl ester at position C-3, was an antibiofilm activity against S. aureus without any effect upon mammalian cells.
publishDate 2019
dc.date.issued.fl_str_mv 2019
dc.date.accessioned.fl_str_mv 2021-11-04T04:24:07Z
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dc.relation.ispartof.pt_BR.fl_str_mv Biomolecules. Basel. Vol. 9. no. 2 (2019), 58, 11 p.
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