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Bone regeneration in sheep model induced by strontium-containing mesoporous bioactive glasses

dc.contributor.authorJiménez Holguín, Javier
dc.contributor.authorLozano Borregón, Daniel
dc.contributor.authorSaiz-Pardo Sanz, Melchor
dc.contributor.authorPablo, David de
dc.contributor.authorOrtega Medina, Luis
dc.contributor.authorPortolés Pérez, María Teresa
dc.contributor.authorArcos Navarrete, Daniel
dc.date.accessioned2025-01-21T10:01:21Z
dc.date.available2025-01-21T10:01:21Z
dc.date.issued2025-01-03
dc.descriptionLa versión aceptada estará en acceso abierto a partir del 1 de abril de 2027
dc.description.abstractLocal delivery of therapeutic ions from bioactive mesoporous glasses (MBGs) is postulated as one of the most promising strategies for regenerative therapy of critical bone defects. Among these ions, Sr2+ cation has been widely considered for this purpose as part of the composition of MBGs. MBGs of chemical composition 75SiO2- 25-x CaO-5P2O5-xSrO with x = 0, 2.5 and 5 (% mol) were prepared by the evaporation induced self-assembly (EISA) method. Strontium incorporation did not affect the apatite forming ability of Sr-free MBG when these bioceramics are treated with simulated body fluid (SBF). In vitro cell viability showed that proliferation of MC3T3-E1 preosteoblast is not affected by the presence of Sr2+ cations, whereas ALP activity and gene expression of Runx2, ALP and VEGF is increased as a function of Sr content. Besides, cell proliferation and VEGF expression of HUVEC cells were also increased with the Sr2+ content. In this work, we present for the first time the effects of Sr containing MBGs on bone regeneration in a large animal model (sheep), after implantation in a cavitary defect. The histomorphometrical analysis and immunohistochemistry indicate that the incorporation of Sr2+ ion greatly enhances the osteoregenerating potential of MBGs. In this sense, the measured ossification areas were 7 % and 20 % for MBG and Sr-MBG, respectively. Besides, the thickness of the newly formed trabeculae was 15 μm and 30 μm for MBG and Sr-MBG, respectively. This enhancement of Sr2+ mediated bone formation would be justified by the transient osteoclastogenesis inhibition and the osteogenesis-angiogenesis increase due to the endothelial cell proliferation and increased vascular endothelial growth factor expression.
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.statuspub
dc.identifier.citationJiménez-Holguín J, Lozano D, Saiz-Pardo M, De Pablo D, Ortega L, Enciso S, et al. Bone regeneration in sheep model induced by strontium-containing mesoporous bioactive glasses. Biomaterials Advances [Internet]. abril de 2025 [citado 21 de enero de 2025];169:214168. Disponible en: https://linkinghub.elsevier.com/retrieve/pii/S2772950824004114
dc.identifier.doi10.1016/j.bioadv.2024.214168
dc.identifier.officialurlhttps://doi.org/10.1016/j.bioadv.2024.214168
dc.identifier.urihttps://hdl.handle.net/20.500.14352/115297
dc.journal.titleBiomaterials Advances
dc.language.isoeng
dc.page.initial214168
dc.relation.projectIDPID2023-149093OB-I00
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-117091RB-I00
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsrestricted access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu615.31
dc.subject.cdu615:54
dc.subject.keywordStrontium
dc.subject.keywordSheep model
dc.subject.keywordBone regeneration
dc.subject.keywordAngiogenesis
dc.subject.keywordMesoporous bioactive glass
dc.subject.ucmQuímica farmaceútica
dc.subject.unesco23 Química
dc.titleBone regeneration in sheep model induced by strontium-containing mesoporous bioactive glasses
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number169
dspace.entity.typePublication
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relation.isAuthorOfPublicationd92c7075-3d31-45ec-a18d-35a5010ee8e1
relation.isAuthorOfPublication.latestForDiscovery82cf0840-5331-47de-a3ab-797fab8b9132

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