Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy

Detalhes bibliográficos
Autor(a) principal: Carriço, Artur da Silva
Data de Publicação: 2016
Outros Autores: Silva-Freitas, Erica L., Pontes, Thales R. F., Araújo-Neto, Rafael P., Damasceno, Ítalo H. M., Silva, Kátia L., Carvalho, Juliana F., Medeiros, Aldo C., Silva, Rodolfo B., Silva, Amanda K. A., Morales, Marco A., Egito, Eryvaldo S. T., Dantas, Ana L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/28791
https://doi.org/10.1208/s12249-016-0673-1
Resumo: The treatment of peptic ulcers induced by H. pylori remains challenging due to the deep mucous layer location of bacteria preventing antimicrobial drug access. The present work aimed to design and evaluate in vitro dual responsive (both pH and magnetic field-sensitive) polymeric magnetic particles loaded with amoxicillin as a smart drug carrier for deep mucous layer penetration and in situ drug release. Magnetite particles were produced by the co-precipitation method and subsequently coated with the Eudragit®S100 and amoxicillin by using the spray-drying technique. The physicochemical characterization of the obtained particles was carried out by optical and scanning electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, nitrogen adsorption/desorption isotherms, and vibrating sample magnetometry. Additionally, drug release tests and antibacterial activity tests were evaluated in vitro. Microparticles presented 17.2 ± 0.4 μm in size and their final composition was 4.3 ± 1.5% of amoxicillin, 87.0 ± 2.3% of Eudragit, and 9.0 ± 0.3% of magnetite. They were both pH and magnetic field responsive while presenting antimicrobial activity. On one side, magnetic field responsiveness of particles is expected to prompt them to reach bacterium niche in deep mucous layer by means of magnetic forces. On the other side, pH responsiveness is expected to enable drug release in the neutral pH of the deep mucous layer, preventing undesired delivery in the acidic gastric lumen. Smart microparticles were designed presenting both pH and magnetic field responsiveness as well as antimicrobial activity. These may be promising assets for peptic ulcer treatment.
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spelling Carriço, Artur da SilvaSilva-Freitas, Erica L.Pontes, Thales R. F.Araújo-Neto, Rafael P.Damasceno, Ítalo H. M.Silva, Kátia L.Carvalho, Juliana F.Medeiros, Aldo C.Silva, Rodolfo B.Silva, Amanda K. A.Morales, Marco A.Egito, Eryvaldo S. T.Dantas, Ana L.2020-04-16T13:10:35Z2020-04-16T13:10:35Z2016-12-13CARRIÇO, Artur da Silva et al. Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy. AAPS PharmSciTech, v. 17, p. 1-11, 2016. ISSN 1530-9932 versão online. DOI https://doi.org/10.1208/s12249-016-0673-1. Disponível em: https://link.springer.com/article/10.1208/s12249-016-0673-1. Acesso em: 8 abr. 2020.1530-9932https://repositorio.ufrn.br/jspui/handle/123456789/28791https://doi.org/10.1208/s12249-016-0673-1Springer Nature Switzerland AGMagnetic polymeric particlesGastric antimicrobial therapyDesign of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapyinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleThe treatment of peptic ulcers induced by H. pylori remains challenging due to the deep mucous layer location of bacteria preventing antimicrobial drug access. The present work aimed to design and evaluate in vitro dual responsive (both pH and magnetic field-sensitive) polymeric magnetic particles loaded with amoxicillin as a smart drug carrier for deep mucous layer penetration and in situ drug release. Magnetite particles were produced by the co-precipitation method and subsequently coated with the Eudragit®S100 and amoxicillin by using the spray-drying technique. The physicochemical characterization of the obtained particles was carried out by optical and scanning electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, nitrogen adsorption/desorption isotherms, and vibrating sample magnetometry. Additionally, drug release tests and antibacterial activity tests were evaluated in vitro. Microparticles presented 17.2 ± 0.4 μm in size and their final composition was 4.3 ± 1.5% of amoxicillin, 87.0 ± 2.3% of Eudragit, and 9.0 ± 0.3% of magnetite. They were both pH and magnetic field responsive while presenting antimicrobial activity. On one side, magnetic field responsiveness of particles is expected to prompt them to reach bacterium niche in deep mucous layer by means of magnetic forces. On the other side, pH responsiveness is expected to enable drug release in the neutral pH of the deep mucous layer, preventing undesired delivery in the acidic gastric lumen. Smart microparticles were designed presenting both pH and magnetic field responsiveness as well as antimicrobial activity. 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dc.title.pt_BR.fl_str_mv Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
title Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
spellingShingle Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
Carriço, Artur da Silva
Magnetic polymeric particles
Gastric antimicrobial therapy
title_short Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
title_full Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
title_fullStr Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
title_full_unstemmed Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
title_sort Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy
author Carriço, Artur da Silva
author_facet Carriço, Artur da Silva
Silva-Freitas, Erica L.
Pontes, Thales R. F.
Araújo-Neto, Rafael P.
Damasceno, Ítalo H. M.
Silva, Kátia L.
Carvalho, Juliana F.
Medeiros, Aldo C.
Silva, Rodolfo B.
Silva, Amanda K. A.
Morales, Marco A.
Egito, Eryvaldo S. T.
Dantas, Ana L.
author_role author
author2 Silva-Freitas, Erica L.
Pontes, Thales R. F.
Araújo-Neto, Rafael P.
Damasceno, Ítalo H. M.
Silva, Kátia L.
Carvalho, Juliana F.
Medeiros, Aldo C.
Silva, Rodolfo B.
Silva, Amanda K. A.
Morales, Marco A.
Egito, Eryvaldo S. T.
Dantas, Ana L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Carriço, Artur da Silva
Silva-Freitas, Erica L.
Pontes, Thales R. F.
Araújo-Neto, Rafael P.
Damasceno, Ítalo H. M.
Silva, Kátia L.
Carvalho, Juliana F.
Medeiros, Aldo C.
Silva, Rodolfo B.
Silva, Amanda K. A.
Morales, Marco A.
Egito, Eryvaldo S. T.
Dantas, Ana L.
dc.subject.por.fl_str_mv Magnetic polymeric particles
Gastric antimicrobial therapy
topic Magnetic polymeric particles
Gastric antimicrobial therapy
description The treatment of peptic ulcers induced by H. pylori remains challenging due to the deep mucous layer location of bacteria preventing antimicrobial drug access. The present work aimed to design and evaluate in vitro dual responsive (both pH and magnetic field-sensitive) polymeric magnetic particles loaded with amoxicillin as a smart drug carrier for deep mucous layer penetration and in situ drug release. Magnetite particles were produced by the co-precipitation method and subsequently coated with the Eudragit®S100 and amoxicillin by using the spray-drying technique. The physicochemical characterization of the obtained particles was carried out by optical and scanning electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, nitrogen adsorption/desorption isotherms, and vibrating sample magnetometry. Additionally, drug release tests and antibacterial activity tests were evaluated in vitro. Microparticles presented 17.2 ± 0.4 μm in size and their final composition was 4.3 ± 1.5% of amoxicillin, 87.0 ± 2.3% of Eudragit, and 9.0 ± 0.3% of magnetite. They were both pH and magnetic field responsive while presenting antimicrobial activity. On one side, magnetic field responsiveness of particles is expected to prompt them to reach bacterium niche in deep mucous layer by means of magnetic forces. On the other side, pH responsiveness is expected to enable drug release in the neutral pH of the deep mucous layer, preventing undesired delivery in the acidic gastric lumen. Smart microparticles were designed presenting both pH and magnetic field responsiveness as well as antimicrobial activity. These may be promising assets for peptic ulcer treatment.
publishDate 2016
dc.date.issued.fl_str_mv 2016-12-13
dc.date.accessioned.fl_str_mv 2020-04-16T13:10:35Z
dc.date.available.fl_str_mv 2020-04-16T13:10:35Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.fl_str_mv CARRIÇO, Artur da Silva et al. Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy. AAPS PharmSciTech, v. 17, p. 1-11, 2016. ISSN 1530-9932 versão online. DOI https://doi.org/10.1208/s12249-016-0673-1. Disponível em: https://link.springer.com/article/10.1208/s12249-016-0673-1. Acesso em: 8 abr. 2020.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/28791
dc.identifier.issn.none.fl_str_mv 1530-9932
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1208/s12249-016-0673-1
identifier_str_mv CARRIÇO, Artur da Silva et al. Design of Magnetic Polymeric Particles as a Stimulus-Responsive System for Gastric Antimicrobial Therapy. AAPS PharmSciTech, v. 17, p. 1-11, 2016. ISSN 1530-9932 versão online. DOI https://doi.org/10.1208/s12249-016-0673-1. Disponível em: https://link.springer.com/article/10.1208/s12249-016-0673-1. Acesso em: 8 abr. 2020.
1530-9932
url https://repositorio.ufrn.br/jspui/handle/123456789/28791
https://doi.org/10.1208/s12249-016-0673-1
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publisher.none.fl_str_mv Springer Nature Switzerland AG
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