Alginate/acemannan-based beads loaded with a biocompatible ionic liquid as a bioactive delivery system
Main Author: | |
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Publication Date: | 2023 |
Other Authors: | , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
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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dc.publisher.none.fl_str_mv |
Elsevier |
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Elsevier |
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