Publication:
Chondroitin and Dermatan Sulfate Bioinks for 3D Bioprinting and Cartilage Regeneration.

dc.contributor.authorLafuente-Merchan, Markel
dc.contributor.authorRuiz-Alonso, Sandra
dc.contributor.authorZabala, Alaitz
dc.contributor.authorGálvez-Martín, Patricia
dc.contributor.authorMarchal, Juan Antonio
dc.contributor.authorVazquez-Lasa, Blanca
dc.contributor.authorGallego, Idoia
dc.contributor.authorSaenz-Del-Burgo, Laura
dc.contributor.authorPedraz, Jose Luis
dc.contributor.funderBasque Country Government.
dc.contributor.funderFundación Mutua Madrileña.
dc.contributor.funderEmpresas y Universidad de la Junta de Andalucía
dc.contributor.funderInstituto de Salud Carlos III.
dc.contributor.funderConsejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía
dc.contributor.funderMinisterio de Economía, Industria y Competitividad, Gobierno de España.
dc.contributor.funderEusko Jaurlaritza.
dc.date.accessioned2023-05-03T15:04:04Z
dc.date.available2023-05-03T15:04:04Z
dc.date.issued2022-01-22
dc.description.abstractCartilage is a connective tissue which a limited capacity for healing and repairing. In this context, osteoarthritis (OA) disease may be developed with high prevalence in which the use of scaffolds may be a promising treatment. In addition, three-dimensional (3D) bioprinting has become an emerging additive manufacturing technology because of its rapid prototyping capacity and the possibility of creating complex structures. This study is focused on the development of nanocellulose-alginate (NC-Alg) based bioinks for 3D bioprinting for cartilage regeneration to which it is added chondroitin sulfate (CS) and dermatan sulfate (DS). First, rheological properties are evaluated. Then, sterilization effect, biocompatibility, and printability on developed NC-Alg-CS and NC-Alg-DS inks are evaluated. Subsequently, printed scaffolds are characterized. Finally, NC-Alg-CS and NC-Alg-DS inks are loaded with murine D1-MSCs-EPO and cell viability and functionality, as well as the chondrogenic differentiation ability are assessed. Results show that the addition of both CS and DS to the NC-Alg ink improves its characteristics in terms of rheology and cell viability and functionality. Moreover, differentiation to cartilage is promoted on NC-Alg-CS and NC-Alg-DS scaffolds. Therefore, the utilization of MSCs containing NC-Alg-CS and NC-Alg-DS scaffolds may become a feasible tissue engineering approach for cartilage regeneration.
dc.identifier.citationLafuente-Merchan M, Ruiz-Alonso S, Zabala A, Gálvez-Martín P, Marchal JA, Vázquez-Lasa B, et al. Chondroitin and Dermatan Sulfate Bioinks for 3D Bioprinting and Cartilage Regeneration. Macromol Biosci. 2022 Mar;22(3):e2100435.
dc.identifier.doi10.1002/mabi.202100435
dc.identifier.essn1616-5195
dc.identifier.issn1616-5195
dc.identifier.pmid35029035
dc.identifier.unpaywallURLhttps://digital.csic.es/bitstream/10261/277842/1/Macromol.%20Biosci.2022%2c22%2c%202100435.pdf
dc.identifier.urihttp://hdl.handle.net/10668/22306
dc.issue.number3
dc.journal.titleMacromolecular bioscience
dc.journal.titleabbreviationMacromol Biosci
dc.language.isoen
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.organizationServicio Andaluz de Salud-SAS
dc.page.number15
dc.provenanceRealizada la curación de contenido 19/08/2024
dc.publisherWiley-VCH Verlag GmbH & Co. KGaA
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDIT907-16
dc.relation.projectIDRTC-2016-5451-1
dc.relation.projectIDB-CTS-230-UGR18
dc.relation.projectIDSOMM17-6109
dc.relation.projectIDP18-FR-2465
dc.relation.projectIDDTS19/00145
dc.relation.projectIDDTS21/00098
dc.relation.projectIDP18-FR-2465
dc.relation.projectIDSOMM17-6109
dc.relation.projectIDB-CTS-230-UGR18
dc.relation.projectIDFMM-AP17196-2019
dc.relation.projectIDIT907-16
dc.relation.projectIDPRE_2020_2_0143
dc.relation.publisherversionhttps://doi.org/10.1002/mabi.202100435
dc.relation.publisherversionThe authors thank the Basque Government for granted fellowship to S. Ruiz-Alonso (PRE_2020_2_0143). This study was financially supported by the Basque Country Government (IT907-16), the Ministerio de Economía, Industria y Competitividad (FEDER funds, project RTC-2016-5451-1). They also wish to thank the intellectual and technical assistance from the ICTS “NANBIOSIS,” more specifically by the Drug Formulation Unit (U10) of the CIBER in Bioengineering, Biomaterials & Nanomedicine (CIBER-BBN) at the University of Basque Country (UPV/EHU). This research was also supported by Fundación Mutua Madrileña (project FMM-AP17196-2019), Consejería de Economía, Conocimiento, Empresas y Universidad de la Junta de Andalucía (ERDF funds, projects B-CTS-230-UGR18, SOMM17-6109, and P18-FR-2465), and the Instituto de Salud Carlos III, ERDF funds (DTS19/00145 and DTS21/00098). The authors also thank to Spanish Ministry of Science and Innovation (MICINN) (project PID2020-114086RB-100). The corresponding author information was updated on March 14, 2022.
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject3D bioprinting
dc.subjectbioinks
dc.subjectcartilage
dc.subjectchondroitin sulfate
dc.subjectdermatan sulfate
dc.subjecttissue engineering
dc.subject.decsAlginatos
dc.subject.decsAndamios del tejido
dc.subject.decsAnimales
dc.subject.decsBioimpresión
dc.subject.decsCartílago
dc.subject.decsCondroitín
dc.subject.decsDermatán Sulfato
dc.subject.decsImpresión tridimensional
dc.subject.decsIngeniería de tejidos
dc.subject.decsRatones
dc.subject.decsRegeneración
dc.subject.meshAlginates
dc.subject.meshAnimals
dc.subject.meshBioprinting
dc.subject.meshCartilage
dc.subject.meshChondroitin
dc.subject.meshDermatan Sulfate
dc.subject.meshMice
dc.subject.meshPrinting, Three-Dimensional
dc.subject.meshRegeneration
dc.subject.meshTissue Engineering
dc.subject.meshTissue Scaffolds
dc.titleChondroitin and Dermatan Sulfate Bioinks for 3D Bioprinting and Cartilage Regeneration.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number22
dspace.entity.typePublication

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