Tuneable spheroidal hydrogel particles for cell and drug encapsulation

Detalhes bibliográficos
Autor(a) principal: Bjorge, Isabel M.
Data de Publicação: 2018
Outros Autores: Costa, Ana M. S., Silva, A. Sofia, Vidal, João P. O., Nóbrega, J. Miguel, Mano, João F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/25682
Resumo: The need to better mimic native tissues has accompanied research in tissue engineering and controlled drug delivery. The development of new platforms for cell and drug encapsulation followed the same trend, and studying the influence of the delivery material system's geometry has been gaining momentum. Aiming to investigate how an increase in surface area and varying particle shape could impact drug release and cell viability, a novel method was developed to produce spheroidal hydrogel particles with adjustable circularity, aiming to tune drug delivery. For this purpose, droplets of hydrogel precursor were squeezed between two superamphiphobic surfaces separated with spacers with different height, and then photo-crosslinked to maintain the acquired shape after "de-sandwiching". Numerical modelling studies were performed to study the polymeric droplet geometry deformation process, which were consistent with experimentally obtained results. The spheroidal particles were produced under mild conditions using methacrylated chitosan, capable of encapsulating proteins or cells. Likely due to their higher surface area to volume-ratio, compared to spherical-shaped ones, spheroids presented an improved viability of encapsulated cells due to enhanced nutrient diffusion to the core, and led to a significantly faster drug release rate from the polymer network. These results were also assessed numerically, in which the drug release rate was computed for different spheroidal-like geometries. Hence, the described method can be used to manufacture spheroidal particles with tailored geometry that can be broadly applied in the biomedical field, including for drug delivery or as cell encapsulation platforms.
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spelling Tuneable spheroidal hydrogel particles for cell and drug encapsulationThe need to better mimic native tissues has accompanied research in tissue engineering and controlled drug delivery. The development of new platforms for cell and drug encapsulation followed the same trend, and studying the influence of the delivery material system's geometry has been gaining momentum. Aiming to investigate how an increase in surface area and varying particle shape could impact drug release and cell viability, a novel method was developed to produce spheroidal hydrogel particles with adjustable circularity, aiming to tune drug delivery. For this purpose, droplets of hydrogel precursor were squeezed between two superamphiphobic surfaces separated with spacers with different height, and then photo-crosslinked to maintain the acquired shape after "de-sandwiching". Numerical modelling studies were performed to study the polymeric droplet geometry deformation process, which were consistent with experimentally obtained results. The spheroidal particles were produced under mild conditions using methacrylated chitosan, capable of encapsulating proteins or cells. Likely due to their higher surface area to volume-ratio, compared to spherical-shaped ones, spheroids presented an improved viability of encapsulated cells due to enhanced nutrient diffusion to the core, and led to a significantly faster drug release rate from the polymer network. These results were also assessed numerically, in which the drug release rate was computed for different spheroidal-like geometries. Hence, the described method can be used to manufacture spheroidal particles with tailored geometry that can be broadly applied in the biomedical field, including for drug delivery or as cell encapsulation platforms.Royal Society of Chemistry2019-01-01T00:00:00Z2018-07-11T00:00:00Z2018-07-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/vnd.openxmlformats-officedocument.wordprocessingml.documenthttp://hdl.handle.net/10773/25682eng1744-683X10.1039/c8sm00921jBjorge, Isabel M.Costa, Ana M. S.Silva, A. SofiaVidal, João P. O.Nóbrega, J. MiguelMano, João F.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:49:45Zoai:ria.ua.pt:10773/25682Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:58:50.806289Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Tuneable spheroidal hydrogel particles for cell and drug encapsulation
title Tuneable spheroidal hydrogel particles for cell and drug encapsulation
spellingShingle Tuneable spheroidal hydrogel particles for cell and drug encapsulation
Bjorge, Isabel M.
title_short Tuneable spheroidal hydrogel particles for cell and drug encapsulation
title_full Tuneable spheroidal hydrogel particles for cell and drug encapsulation
title_fullStr Tuneable spheroidal hydrogel particles for cell and drug encapsulation
title_full_unstemmed Tuneable spheroidal hydrogel particles for cell and drug encapsulation
title_sort Tuneable spheroidal hydrogel particles for cell and drug encapsulation
author Bjorge, Isabel M.
author_facet Bjorge, Isabel M.
Costa, Ana M. S.
Silva, A. Sofia
Vidal, João P. O.
Nóbrega, J. Miguel
Mano, João F.
author_role author
author2 Costa, Ana M. S.
Silva, A. Sofia
Vidal, João P. O.
Nóbrega, J. Miguel
Mano, João F.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Bjorge, Isabel M.
Costa, Ana M. S.
Silva, A. Sofia
Vidal, João P. O.
Nóbrega, J. Miguel
Mano, João F.
description The need to better mimic native tissues has accompanied research in tissue engineering and controlled drug delivery. The development of new platforms for cell and drug encapsulation followed the same trend, and studying the influence of the delivery material system's geometry has been gaining momentum. Aiming to investigate how an increase in surface area and varying particle shape could impact drug release and cell viability, a novel method was developed to produce spheroidal hydrogel particles with adjustable circularity, aiming to tune drug delivery. For this purpose, droplets of hydrogel precursor were squeezed between two superamphiphobic surfaces separated with spacers with different height, and then photo-crosslinked to maintain the acquired shape after "de-sandwiching". Numerical modelling studies were performed to study the polymeric droplet geometry deformation process, which were consistent with experimentally obtained results. The spheroidal particles were produced under mild conditions using methacrylated chitosan, capable of encapsulating proteins or cells. Likely due to their higher surface area to volume-ratio, compared to spherical-shaped ones, spheroids presented an improved viability of encapsulated cells due to enhanced nutrient diffusion to the core, and led to a significantly faster drug release rate from the polymer network. These results were also assessed numerically, in which the drug release rate was computed for different spheroidal-like geometries. Hence, the described method can be used to manufacture spheroidal particles with tailored geometry that can be broadly applied in the biomedical field, including for drug delivery or as cell encapsulation platforms.
publishDate 2018
dc.date.none.fl_str_mv 2018-07-11T00:00:00Z
2018-07-11
2019-01-01T00:00:00Z
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url http://hdl.handle.net/10773/25682
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dc.relation.none.fl_str_mv 1744-683X
10.1039/c8sm00921j
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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