Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy

Detalhes bibliográficos
Autor(a) principal: Campos, Estefânia V. R.
Data de Publicação: 2022
Outros Autores: Proença, Patrícia L. F. [UNESP], Costa, Tais G. da, Lima, Renata de, Fraceto, Leonardo F. [UNESP], Araujo, Daniele R. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1155/2022/9165443
http://hdl.handle.net/11449/240847
Resumo: Topical delivery of local anesthetics (LAs) is commonly used to decrease painful sensations, block pain throughout procedures, and alleviate pain after surgery. Dermal and/or transdermal delivery of LAs has other advantages, such as sustained drug delivery and decreased systemic adverse effects. This study reports the development of poly(D,L-lactide-co-glycolide) (PLGA) nanoparticles coated with chitosan for the sustained release and topicality of benzocaine (BZC) and topical delivery. BZC PLGA nanoparticles or nonencapsulated drugs were further incorporated into Poloxamer hydrogels (Pluronic™ F-127). The nanoparticles showed a mean diameter of 380±4 nm, positive zeta potential after coating with chitosan (23.3±1.7 mV), and high encapsulation efficiency (96.7±0.02%). Cellular viability greater than 70% for both fibroblasts and keratinocytes was observed after treatment with nanoparticles, which is in accordance with the preconized guidelines for biomedical devices and delivery systems. Both the nanoparticles and hydrogels were able to modulate BZC delivery and increase drug permeation when compared to the nonencapsulated drug. Furthermore, the incorporation of limonene into hydrogels containing BZC-loaded nanoparticles increased the BZC permeation rates. Non-Newtonian and pseudoplastic behaviors were observed for all hydrogel nanoformulations with or without nanoparticles. These results demonstrate that the hydrogel-nanoparticle hybrids could be a promising delivery system for prolonged local anesthetic therapy.
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spelling Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery StrategyTopical delivery of local anesthetics (LAs) is commonly used to decrease painful sensations, block pain throughout procedures, and alleviate pain after surgery. Dermal and/or transdermal delivery of LAs has other advantages, such as sustained drug delivery and decreased systemic adverse effects. This study reports the development of poly(D,L-lactide-co-glycolide) (PLGA) nanoparticles coated with chitosan for the sustained release and topicality of benzocaine (BZC) and topical delivery. BZC PLGA nanoparticles or nonencapsulated drugs were further incorporated into Poloxamer hydrogels (Pluronic™ F-127). The nanoparticles showed a mean diameter of 380±4 nm, positive zeta potential after coating with chitosan (23.3±1.7 mV), and high encapsulation efficiency (96.7±0.02%). Cellular viability greater than 70% for both fibroblasts and keratinocytes was observed after treatment with nanoparticles, which is in accordance with the preconized guidelines for biomedical devices and delivery systems. Both the nanoparticles and hydrogels were able to modulate BZC delivery and increase drug permeation when compared to the nonencapsulated drug. Furthermore, the incorporation of limonene into hydrogels containing BZC-loaded nanoparticles increased the BZC permeation rates. Non-Newtonian and pseudoplastic behaviors were observed for all hydrogel nanoformulations with or without nanoparticles. These results demonstrate that the hydrogel-nanoparticle hybrids could be a promising delivery system for prolonged local anesthetic therapy.Human and Natural and Sciences Center Federal University of ABC, SPDrugs and Bioactives Delivery Systems Research Group-SISLIBIO Federal University of ABCSão Paulo State University (UNESP) Laboratory of Environmental Nanotechnology Institute of Science and Technology of Sorocaba, SPLABiToN (Laboratory of Bioactivity Assessment and Toxicology of Nanomaterials) University of Sorocaba, SPSão Paulo State University (UNESP) Laboratory of Environmental Nanotechnology Institute of Science and Technology of Sorocaba, SPUniversidade Federal do ABC (UFABC)Universidade Estadual Paulista (UNESP)University of SorocabaCampos, Estefânia V. R.Proença, Patrícia L. F. [UNESP]Costa, Tais G. daLima, Renata deFraceto, Leonardo F. [UNESP]Araujo, Daniele R. de2023-03-01T20:35:23Z2023-03-01T20:35:23Z2022-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1155/2022/9165443BioMed Research International, v. 2022.2314-61412314-6133http://hdl.handle.net/11449/24084710.1155/2022/91654432-s2.0-85128368422Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBioMed Research Internationalinfo:eu-repo/semantics/openAccess2023-03-01T20:35:23Zoai:repositorio.unesp.br:11449/240847Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:19:36.726129Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
title Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
spellingShingle Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
Campos, Estefânia V. R.
title_short Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
title_full Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
title_fullStr Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
title_full_unstemmed Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
title_sort Using Chitosan-Coated Polymeric Nanoparticles-Thermosensitive Hydrogels in association with Limonene as Skin Drug Delivery Strategy
author Campos, Estefânia V. R.
author_facet Campos, Estefânia V. R.
Proença, Patrícia L. F. [UNESP]
Costa, Tais G. da
Lima, Renata de
Fraceto, Leonardo F. [UNESP]
Araujo, Daniele R. de
author_role author
author2 Proença, Patrícia L. F. [UNESP]
Costa, Tais G. da
Lima, Renata de
Fraceto, Leonardo F. [UNESP]
Araujo, Daniele R. de
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do ABC (UFABC)
Universidade Estadual Paulista (UNESP)
University of Sorocaba
dc.contributor.author.fl_str_mv Campos, Estefânia V. R.
Proença, Patrícia L. F. [UNESP]
Costa, Tais G. da
Lima, Renata de
Fraceto, Leonardo F. [UNESP]
Araujo, Daniele R. de
description Topical delivery of local anesthetics (LAs) is commonly used to decrease painful sensations, block pain throughout procedures, and alleviate pain after surgery. Dermal and/or transdermal delivery of LAs has other advantages, such as sustained drug delivery and decreased systemic adverse effects. This study reports the development of poly(D,L-lactide-co-glycolide) (PLGA) nanoparticles coated with chitosan for the sustained release and topicality of benzocaine (BZC) and topical delivery. BZC PLGA nanoparticles or nonencapsulated drugs were further incorporated into Poloxamer hydrogels (Pluronic™ F-127). The nanoparticles showed a mean diameter of 380±4 nm, positive zeta potential after coating with chitosan (23.3±1.7 mV), and high encapsulation efficiency (96.7±0.02%). Cellular viability greater than 70% for both fibroblasts and keratinocytes was observed after treatment with nanoparticles, which is in accordance with the preconized guidelines for biomedical devices and delivery systems. Both the nanoparticles and hydrogels were able to modulate BZC delivery and increase drug permeation when compared to the nonencapsulated drug. Furthermore, the incorporation of limonene into hydrogels containing BZC-loaded nanoparticles increased the BZC permeation rates. Non-Newtonian and pseudoplastic behaviors were observed for all hydrogel nanoformulations with or without nanoparticles. These results demonstrate that the hydrogel-nanoparticle hybrids could be a promising delivery system for prolonged local anesthetic therapy.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
2023-03-01T20:35:23Z
2023-03-01T20:35:23Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1155/2022/9165443
BioMed Research International, v. 2022.
2314-6141
2314-6133
http://hdl.handle.net/11449/240847
10.1155/2022/9165443
2-s2.0-85128368422
url http://dx.doi.org/10.1155/2022/9165443
http://hdl.handle.net/11449/240847
identifier_str_mv BioMed Research International, v. 2022.
2314-6141
2314-6133
10.1155/2022/9165443
2-s2.0-85128368422
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BioMed Research International
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reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
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reponame_str Repositório Institucional da UNESP
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repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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