Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system

Bibliographic Details
Main Author: Gomes, Joana M.
Publication Date: 2023
Other Authors: Silva, SS, Rodrigues, Luísa Cidália Guimarães, Reis, R. L.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/1822/85408
Summary: Combining biomacromolecules with green chemistry principles and clean technologies has proven to be an effective approach for drug delivery, providing a prolonged and sustained release of the encapsulated material. The current study investigates the potential of cholinium caffeate (Ch[Caffeate]), a phenolic-based biocompatible ionic liquid (Bio-IL) entrapped in alginate/acemannan beads, as a drug delivery system able to reduce local joint inflammation on osteoarthritis (OA) treatment. The synthesized Bio-IL has antioxidant and anti-inflammatory actions that, combined with biopolymers as 3D architectures, promote the entrapment and sustainable release of the bioactive molecules over time. The physicochemical and morphological characterization of the beads (ALC, ALAC0,5, ALAC1, and ALAC3, containing 0, 0.5, 1, and 3 %(w/v) of Ch[Caffeate], respectively) revealed a porous and interconnected structure, with medium pore sizes ranging from 209.16 to 221.30 μm, with a high swelling ability (up 2400 %). Ch[Caffeate] significantly improved the antioxidant activities of the constructs by 95 % and 97 % for ALAC1 and ALAC3, respectively, when compared to ALA (56 %). Besides, the structures provided the environment for ATDC5 cell proliferation, and cartilage-like ECM formation, supported by the increased GAGs in ALAC1 and ALAC3 formulations after 21 days. Further, the ability to block the secretion of pro-inflammatory cytokines (TNF-α and IL-6), from differentiated THP-1 was evidenced by ChAL-Ch[Caffeate] beads. These outcomes suggest that the established strategy based on using natural and bioactive macromolecules to develop 3D constructs has great potential to be used as therapeutic tools for patients with OA.
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spelling Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery systemAcemannanAlginateBiocompatible ionic liquidsCholinium caffeicOsteoarthritisCombining biomacromolecules with green chemistry principles and clean technologies has proven to be an effective approach for drug delivery, providing a prolonged and sustained release of the encapsulated material. The current study investigates the potential of cholinium caffeate (Ch[Caffeate]), a phenolic-based biocompatible ionic liquid (Bio-IL) entrapped in alginate/acemannan beads, as a drug delivery system able to reduce local joint inflammation on osteoarthritis (OA) treatment. The synthesized Bio-IL has antioxidant and anti-inflammatory actions that, combined with biopolymers as 3D architectures, promote the entrapment and sustainable release of the bioactive molecules over time. The physicochemical and morphological characterization of the beads (ALC, ALAC0,5, ALAC1, and ALAC3, containing 0, 0.5, 1, and 3 %(w/v) of Ch[Caffeate], respectively) revealed a porous and interconnected structure, with medium pore sizes ranging from 209.16 to 221.30 μm, with a high swelling ability (up 2400 %). Ch[Caffeate] significantly improved the antioxidant activities of the constructs by 95 % and 97 % for ALAC1 and ALAC3, respectively, when compared to ALA (56 %). Besides, the structures provided the environment for ATDC5 cell proliferation, and cartilage-like ECM formation, supported by the increased GAGs in ALAC1 and ALAC3 formulations after 21 days. Further, the ability to block the secretion of pro-inflammatory cytokines (TNF-α and IL-6), from differentiated THP-1 was evidenced by ChAL-Ch[Caffeate] beads. These outcomes suggest that the established strategy based on using natural and bioactive macromolecules to develop 3D constructs has great potential to be used as therapeutic tools for patients with OA.The authors especially acknowledge financial support from Portuguese Fundação para a Ciência e Tecnologia (FCT) (PD/BD/135247/2017, SFRH/BPD/93697/2013 and CEECIND/01306/2018). This work is also financially supported by PhD Programme in Advanced Therapies for Health (PATH) (PD/00169/2013), FCT R&D&I projects with references PTDC/BII-BIO/31570/2017, PTDC/CTM-CTM/29813/2017, and R&D&I Structured Projects with reference NORTE-01-0145-FDER000021.ElsevierUniversidade do MinhoGomes, Joana M.Silva, SSRodrigues, Luísa Cidália GuimarãesReis, R. L.2023-052023-05-01T00:00:00Z2025-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/85408engGomes J. M., Silva S. S., Rodrigues L.C., Reis R. L. Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system, International Journal Of Biological Macromolecules, Vol. 242, pp. 125026, doi:https://doi.org/10.1016/j.ijbiomac.2023.125026, 20230141-813010.1016/j.ijbiomac.2023.12502637244345125026https://www.sciencedirect.com/science/article/pii/S0141813023019207?via%3Dihubinfo:eu-repo/semantics/embargoedAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-04-12T05:15:03Zoai:repositorium.sdum.uminho.pt:1822/85408Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T16:16:49.685884Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
title Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
spellingShingle Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
Gomes, Joana M.
Acemannan
Alginate
Biocompatible ionic liquids
Cholinium caffeic
Osteoarthritis
title_short Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
title_full Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
title_fullStr Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
title_full_unstemmed Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
title_sort Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
author Gomes, Joana M.
author_facet Gomes, Joana M.
Silva, SS
Rodrigues, Luísa Cidália Guimarães
Reis, R. L.
author_role author
author2 Silva, SS
Rodrigues, Luísa Cidália Guimarães
Reis, R. L.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Gomes, Joana M.
Silva, SS
Rodrigues, Luísa Cidália Guimarães
Reis, R. L.
dc.subject.por.fl_str_mv Acemannan
Alginate
Biocompatible ionic liquids
Cholinium caffeic
Osteoarthritis
topic Acemannan
Alginate
Biocompatible ionic liquids
Cholinium caffeic
Osteoarthritis
description Combining biomacromolecules with green chemistry principles and clean technologies has proven to be an effective approach for drug delivery, providing a prolonged and sustained release of the encapsulated material. The current study investigates the potential of cholinium caffeate (Ch[Caffeate]), a phenolic-based biocompatible ionic liquid (Bio-IL) entrapped in alginate/acemannan beads, as a drug delivery system able to reduce local joint inflammation on osteoarthritis (OA) treatment. The synthesized Bio-IL has antioxidant and anti-inflammatory actions that, combined with biopolymers as 3D architectures, promote the entrapment and sustainable release of the bioactive molecules over time. The physicochemical and morphological characterization of the beads (ALC, ALAC0,5, ALAC1, and ALAC3, containing 0, 0.5, 1, and 3 %(w/v) of Ch[Caffeate], respectively) revealed a porous and interconnected structure, with medium pore sizes ranging from 209.16 to 221.30 μm, with a high swelling ability (up 2400 %). Ch[Caffeate] significantly improved the antioxidant activities of the constructs by 95 % and 97 % for ALAC1 and ALAC3, respectively, when compared to ALA (56 %). Besides, the structures provided the environment for ATDC5 cell proliferation, and cartilage-like ECM formation, supported by the increased GAGs in ALAC1 and ALAC3 formulations after 21 days. Further, the ability to block the secretion of pro-inflammatory cytokines (TNF-α and IL-6), from differentiated THP-1 was evidenced by ChAL-Ch[Caffeate] beads. These outcomes suggest that the established strategy based on using natural and bioactive macromolecules to develop 3D constructs has great potential to be used as therapeutic tools for patients with OA.
publishDate 2023
dc.date.none.fl_str_mv 2023-05
2023-05-01T00:00:00Z
2025-06-01T00:00:00Z
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/85408
url https://hdl.handle.net/1822/85408
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Gomes J. M., Silva S. S., Rodrigues L.C., Reis R. L. Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system, International Journal Of Biological Macromolecules, Vol. 242, pp. 125026, doi:https://doi.org/10.1016/j.ijbiomac.2023.125026, 2023
0141-8130
10.1016/j.ijbiomac.2023.125026
37244345
125026
https://www.sciencedirect.com/science/article/pii/S0141813023019207?via%3Dihub
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