Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/pharmaceutics12080695 http://hdl.handle.net/11449/195639 |
Resumo: | Bacterial resistance has become an important public health problem. Bacteria have been acquiring mechanisms to resist the action of antimicrobial active pharmaceutical ingredients (API). Based on this, a promising alternative is the use of nanotechnology, since when the systems are presented in nanometric size, there is an increase in the interaction and concentration of the action at the target site improving the activity. Thus, this study aims to develop a polymeric nanoparticle (PN) composed of chitosan and hydroxypropylmethylcellulose, as an innovative strategy for the administration of an association between ceftriaxone and extract ofS. brasiliensis, for the treatment of Enterobacteriaceae. From a Box-Behnken design, nanoparticles were obtained and evaluated using the DLS technique, obtaining the particle size between 440 and 1660 nm, IPD from 0.42 to 0.92, and positive charges. Morphological characteristics of PN by SEM revealed spherical morphology and sizes similar to DLS. Infrared spectroscopy showed no chemical interaction between the components of the formulation. The broth microdilution technique evaluated their antimicrobial activity, and a considerable improvement in the activity of the extract and the API compared to the free compounds was found, reaching an improvement of 133 times in the minimum inhibitory activity CRO. |
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Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteriabacterial resistanceEnterobacteriaceaechitosanHPMCBacterial resistance has become an important public health problem. Bacteria have been acquiring mechanisms to resist the action of antimicrobial active pharmaceutical ingredients (API). Based on this, a promising alternative is the use of nanotechnology, since when the systems are presented in nanometric size, there is an increase in the interaction and concentration of the action at the target site improving the activity. Thus, this study aims to develop a polymeric nanoparticle (PN) composed of chitosan and hydroxypropylmethylcellulose, as an innovative strategy for the administration of an association between ceftriaxone and extract ofS. brasiliensis, for the treatment of Enterobacteriaceae. From a Box-Behnken design, nanoparticles were obtained and evaluated using the DLS technique, obtaining the particle size between 440 and 1660 nm, IPD from 0.42 to 0.92, and positive charges. Morphological characteristics of PN by SEM revealed spherical morphology and sizes similar to DLS. Infrared spectroscopy showed no chemical interaction between the components of the formulation. The broth microdilution technique evaluated their antimicrobial activity, and a considerable improvement in the activity of the extract and the API compared to the free compounds was found, reaching an improvement of 133 times in the minimum inhibitory activity CRO.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Estadual Paraiba, Ctr Ciencias Biol & Saude, Lab Desenvolvimento & Ensaios Medicamentos, R Baraunas 351,Cidade Univ, BR-58429500 Campina Grande, Paraiba, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Km 1, BR-14800903 Araraquara, SP, BrazilUniv Fed Paraiba, Ctr Tecnol & Desenvolvimento Reg, Av Escoteiros S-N,Mangabeira 7, BR-58055000 Joao Pessoa, Paraiba, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Km 1, BR-14800903 Araraquara, SP, BrazilCAPES: 001MdpiUniv Estadual ParaibaUniversidade Estadual Paulista (Unesp)Univ Fed ParaibaOliveira, Maisa Soares deOshiro-Junior, Joao AugustoSato, Mariana Rillo [UNESP]Conceicao, Marta MariaDantas Medeiros, Ana Claudia2020-12-10T17:41:25Z2020-12-10T17:41:25Z2020-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article18http://dx.doi.org/10.3390/pharmaceutics12080695Pharmaceutics. Basel: Mdpi, v. 12, n. 8, 18 p., 2020.http://hdl.handle.net/11449/19563910.3390/pharmaceutics12080695WOS:000564055900001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPharmaceuticsinfo:eu-repo/semantics/openAccess2021-10-23T10:02:24Zoai:repositorio.unesp.br:11449/195639Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:41:09.569095Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
title |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
spellingShingle |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria Oliveira, Maisa Soares de bacterial resistance Enterobacteriaceae chitosan HPMC |
title_short |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
title_full |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
title_fullStr |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
title_full_unstemmed |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
title_sort |
Polymeric Nanoparticle Associated with Ceftriaxone and Extract of Schinopsis Brasiliensis Engler againstMultiresistant Enterobacteria |
author |
Oliveira, Maisa Soares de |
author_facet |
Oliveira, Maisa Soares de Oshiro-Junior, Joao Augusto Sato, Mariana Rillo [UNESP] Conceicao, Marta Maria Dantas Medeiros, Ana Claudia |
author_role |
author |
author2 |
Oshiro-Junior, Joao Augusto Sato, Mariana Rillo [UNESP] Conceicao, Marta Maria Dantas Medeiros, Ana Claudia |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Univ Estadual Paraiba Universidade Estadual Paulista (Unesp) Univ Fed Paraiba |
dc.contributor.author.fl_str_mv |
Oliveira, Maisa Soares de Oshiro-Junior, Joao Augusto Sato, Mariana Rillo [UNESP] Conceicao, Marta Maria Dantas Medeiros, Ana Claudia |
dc.subject.por.fl_str_mv |
bacterial resistance Enterobacteriaceae chitosan HPMC |
topic |
bacterial resistance Enterobacteriaceae chitosan HPMC |
description |
Bacterial resistance has become an important public health problem. Bacteria have been acquiring mechanisms to resist the action of antimicrobial active pharmaceutical ingredients (API). Based on this, a promising alternative is the use of nanotechnology, since when the systems are presented in nanometric size, there is an increase in the interaction and concentration of the action at the target site improving the activity. Thus, this study aims to develop a polymeric nanoparticle (PN) composed of chitosan and hydroxypropylmethylcellulose, as an innovative strategy for the administration of an association between ceftriaxone and extract ofS. brasiliensis, for the treatment of Enterobacteriaceae. From a Box-Behnken design, nanoparticles were obtained and evaluated using the DLS technique, obtaining the particle size between 440 and 1660 nm, IPD from 0.42 to 0.92, and positive charges. Morphological characteristics of PN by SEM revealed spherical morphology and sizes similar to DLS. Infrared spectroscopy showed no chemical interaction between the components of the formulation. The broth microdilution technique evaluated their antimicrobial activity, and a considerable improvement in the activity of the extract and the API compared to the free compounds was found, reaching an improvement of 133 times in the minimum inhibitory activity CRO. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-10T17:41:25Z 2020-12-10T17:41:25Z 2020-08-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/pharmaceutics12080695 Pharmaceutics. Basel: Mdpi, v. 12, n. 8, 18 p., 2020. http://hdl.handle.net/11449/195639 10.3390/pharmaceutics12080695 WOS:000564055900001 |
url |
http://dx.doi.org/10.3390/pharmaceutics12080695 http://hdl.handle.net/11449/195639 |
identifier_str_mv |
Pharmaceutics. Basel: Mdpi, v. 12, n. 8, 18 p., 2020. 10.3390/pharmaceutics12080695 WOS:000564055900001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Pharmaceutics |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
18 |
dc.publisher.none.fl_str_mv |
Mdpi |
publisher.none.fl_str_mv |
Mdpi |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128686765899776 |