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Design of polymeric core-shell carriers for combination therapies

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Resumo:Particle engineering for co-delivery of drugs has the potential to combine multiple drugs with different pharmaceutical mechanisms within the same carrier, increasing the therapeutic efficiency while improving patient compliance. This work proposes a novel approach for producing polymer–polymer core–shell microparticles by multi-step processing of emulsion and spray drying. The particle core was obtained by an oil-in-water emulsion of poly(ε-caprolactone) (PCL) loaded with curcumin (CM), followed by the resuspension in poly(vinyl alcohol) (PVA) containing ciprofloxacin (CPx) forming the shell layer by spray-drying. The obtained core-shell particles showed an average size of 3.8 ± 1.2 μm, which is a suitable size for inhalation therapies. The spatial distribution of the drugs was studied using synchrotron-based macro attenuated total reflection Fourier transform infrared (macro ATR-FTIR) microspectroscopy to map the chemical distribution of the components within the particles and supported the presence of CM and CPx in the core and shell layers, respectively. The formation of the core–shell structure was further supported by the differences in the release profile of CM from these particles, when compared to the release profile observed for the single particle structure (PCL-CM). Both empty and drug-loaded carriers (up to 100 μg.mL−1) showed no cytotoxic effects on A549 cells while exhibiting the antibacterial activity of CPx against Gram-positive and Gram-negative bacteria. These polymer core–shell microparticles provide a promising route for the combination and sequential drug release therapies, with the potential to be used in inhalation therapies
Autores principais:Silva, Dina M.
Outros Autores:Liu, Ruy; Gonçalves, Anabela F.; da Costa, André; Gomes, Andreia C; Machado, Raúl; Vongsvivut, Jitraporn; Tobin, Mark J.; Sencadas, Vítor João Gomes Silva
Assunto:Biodegradable polymers Controlled drug delivery Combination therapies Core-shell particles Inhalation therapies Antimicrobial activity Electrospinning Lactoferrin Nanofiber membranes Poly(lactic acid)
Ano:2021
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Silva, Dina M.
author2 Liu, Ruy
Gonçalves, Anabela F.
da Costa, André
Gomes, Andreia C
Machado, Raúl
Vongsvivut, Jitraporn
Tobin, Mark J.
Sencadas, Vítor João Gomes Silva
author2_role author
author
author
author
author
author
author
author
author_facet Silva, Dina M.
Liu, Ruy
Gonçalves, Anabela F.
da Costa, André
Gomes, Andreia C
Machado, Raúl
Vongsvivut, Jitraporn
Tobin, Mark J.
Sencadas, Vítor João Gomes Silva
author_role author
contributor_name_str_mv Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Silva, Dina M.\"},{\"Person.name\":\"Liu, Ruy\"},{\"Person.name\":\"Gonçalves, Anabela F.\"},{\"Person.name\":\"da Costa, André\"},{\"Person.name\":\"Gomes, Andreia C\"},{\"Person.name\":\"Machado, Raúl\"},{\"Person.name\":\"Vongsvivut, Jitraporn\"},{\"Person.name\":\"Tobin, Mark J.\"},{\"Person.name\":\"Sencadas, Vítor João Gomes Silva\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Universidade do Minho
datacite.creators.creator.creatorName.fl_str_mv Silva, Dina M.
Liu, Ruy
Gonçalves, Anabela F.
da Costa, André
Gomes, Andreia C
Machado, Raúl
Vongsvivut, Jitraporn
Tobin, Mark J.
Sencadas, Vítor João Gomes Silva
datacite.date.Accepted.fl_str_mv 2021-01-01T00:00:00Z
datacite.date.embargoed.fl_str_mv 10000-01-01T00:00:00Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_16ec
datacite.subjects.subject.fl_str_mv Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
datacite.titles.title.fl_str_mv Design of polymeric core-shell carriers for combination therapies
dc.contributor.none.fl_str_mv Universidade do Minho
dc.creator.none.fl_str_mv Silva, Dina M.
Liu, Ruy
Gonçalves, Anabela F.
da Costa, André
Gomes, Andreia C
Machado, Raúl
Vongsvivut, Jitraporn
Tobin, Mark J.
Sencadas, Vítor João Gomes Silva
dc.date.Accepted.fl_str_mv 2021-01-01T00:00:00Z
dc.date.embargoed.fl_str_mv 10000-01-01T00:00:00Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/73095
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Elsevier
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.subject.none.fl_str_mv Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
dc.title.fl_str_mv Design of polymeric core-shell carriers for combination therapies
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Particle engineering for co-delivery of drugs has the potential to combine multiple drugs with different pharmaceutical mechanisms within the same carrier, increasing the therapeutic efficiency while improving patient compliance. This work proposes a novel approach for producing polymer–polymer core–shell microparticles by multi-step processing of emulsion and spray drying. The particle core was obtained by an oil-in-water emulsion of poly(ε-caprolactone) (PCL) loaded with curcumin (CM), followed by the resuspension in poly(vinyl alcohol) (PVA) containing ciprofloxacin (CPx) forming the shell layer by spray-drying. The obtained core-shell particles showed an average size of 3.8 ± 1.2 μm, which is a suitable size for inhalation therapies. The spatial distribution of the drugs was studied using synchrotron-based macro attenuated total reflection Fourier transform infrared (macro ATR-FTIR) microspectroscopy to map the chemical distribution of the components within the particles and supported the presence of CM and CPx in the core and shell layers, respectively. The formation of the core–shell structure was further supported by the differences in the release profile of CM from these particles, when compared to the release profile observed for the single particle structure (PCL-CM). Both empty and drug-loaded carriers (up to 100 μg.mL−1) showed no cytotoxic effects on A549 cells while exhibiting the antibacterial activity of CPx against Gram-positive and Gram-negative bacteria. These polymer core–shell microparticles provide a promising route for the combination and sequential drug release therapies, with the potential to be used in inhalation therapies
dirty 0
eu_rights_str_mv restrictedAccess
format article
fulltext.url.fl_str_mv https://prod-dspace.uminho.pt/bitstreams/39a599ea-e332-4691-8ed1-ac8d53fc5735/download
id rum_50aacbd2220fa9e1e2df9032dfd7d53f
identifier.url.fl_str_mv https://hdl.handle.net/1822/73095
instacron_str repositorium
institution Universidade do Minho
instname_str Universidade do Minho
language eng
network_acronym_str rum
network_name_str RepositóriUM - Universidade do Minho
oai_identifier_str oai:repositorium.uminho.pt:1822/73095
organization_str_mv urn:organizationAcronym:repositorium
person_str_mv Silva, Dina M.
Liu, Ruy
Gonçalves, Anabela F.
da Costa, André
Gomes, Andreia C
Machado, Raúl
Vongsvivut, Jitraporn
Tobin, Mark J.
Sencadas, Vítor João Gomes Silva
publishDate 2021
publisher.none.fl_str_mv Elsevier
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engElsevierporParticle engineering for co-delivery of drugs has the potential to combine multiple drugs with different pharmaceutical mechanisms within the same carrier, increasing the therapeutic efficiency while improving patient compliance. This work proposes a novel approach for producing polymer–polymer core–shell microparticles by multi-step processing of emulsion and spray drying. The particle core was obtained by an oil-in-water emulsion of poly(ε-caprolactone) (PCL) loaded with curcumin (CM), followed by the resuspension in poly(vinyl alcohol) (PVA) containing ciprofloxacin (CPx) forming the shell layer by spray-drying. The obtained core-shell particles showed an average size of 3.8 ± 1.2 μm, which is a suitable size for inhalation therapies. The spatial distribution of the drugs was studied using synchrotron-based macro attenuated total reflection Fourier transform infrared (macro ATR-FTIR) microspectroscopy to map the chemical distribution of the components within the particles and supported the presence of CM and CPx in the core and shell layers, respectively. The formation of the core–shell structure was further supported by the differences in the release profile of CM from these particles, when compared to the release profile observed for the single particle structure (PCL-CM). Both empty and drug-loaded carriers (up to 100 μg.mL−1) showed no cytotoxic effects on A549 cells while exhibiting the antibacterial activity of CPx against Gram-positive and Gram-negative bacteria. These polymer core–shell microparticles provide a promising route for the combination and sequential drug release therapies, with the potential to be used in inhalation therapiesapplication/pdfporDesign of polymeric core-shell carriers for combination therapiesSilva, Dina M.Liu, RuyGonçalves, Anabela F.da Costa, AndréGomes, Andreia CMachado, RaúlVongsvivut, JitrapornTobin, Mark J.Sencadas, Vítor João Gomes SilvaHostingInstitutionOrganizationalUniversidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptISSNIsPartOf1616-5187DOIIsPartOf10.1016/j.jcis.2020.12.00120212021-05-24T23:14:16Z10000-01-01T00:00:00Z2021-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/73095http://purl.org/coar/access_right/c_16ecrestricted accessBiodegradable polymersControlled drug deliveryCombination therapiesCore-shell particlesInhalation therapiesAntimicrobial activityElectrospinningLactoferrinNanofiber membranesPoly(lactic acid)3133055 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_f1cfapplication/pdffulltexthttps://prod-dspace.uminho.pt/bitstreams/39a599ea-e332-4691-8ed1-ac8d53fc5735/download
spellingShingle Design of polymeric core-shell carriers for combination therapies
Silva, Dina M.
Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
status SINGLETON
subject.fl_str_mv Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
title Design of polymeric core-shell carriers for combination therapies
title_full Design of polymeric core-shell carriers for combination therapies
title_fullStr Design of polymeric core-shell carriers for combination therapies
title_full_unstemmed Design of polymeric core-shell carriers for combination therapies
title_short Design of polymeric core-shell carriers for combination therapies
title_sort Design of polymeric core-shell carriers for combination therapies
topic Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
topic_facet Biodegradable polymers
Controlled drug delivery
Combination therapies
Core-shell particles
Inhalation therapies
Antimicrobial activity
Electrospinning
Lactoferrin
Nanofiber membranes
Poly(lactic acid)
url https://hdl.handle.net/1822/73095
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