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dc.contributor.authorSteffaine Rappe, Katrin
dc.contributor.authorOrtiz Hernández, Mónica
dc.contributor.authorPunset Fuste, Miquel
dc.contributor.authorMolmeneu Trias, Meritxell
dc.contributor.authorBarba Serrahima, Albert
dc.contributor.authorMas Moruno, Carlos
dc.contributor.authorGuillem Martí, Jordi
dc.contributor.authorCaparrós, Cristina
dc.contributor.authorRupérez de Gracia, Elisa
dc.contributor.authorCalero, José
dc.contributor.authorManzanares, Maria Cristina
dc.contributor.authorGil Mur, Javier
dc.contributor.authorFranch, Jordi
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Ciència i Enginyeria de Materials
dc.date.accessioned2022-07-14T12:35:27Z
dc.date.available2022-07-14T12:35:27Z
dc.date.issued2022-02-01
dc.identifier.citationKatrin S. Rappe [et al.]. On-growth and in-growth osseointegration enhancement in PM porous Ti-scaffolds by two different bioactivation strategies: alkali thermochemical treatment and RGD peptide coating. "International journal of molecular sciences", 1 Febrer 2022, vol. 23, núm. 1750.
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/2117/370206
dc.description.abstractA lack of primary stability and osteointegration in metallic implants may result in implant loosening and failure. Adding porosity to metallic implants reduces the stress shielding effect and improves implant performance, allowing the surrounding bone tissue to grow into the scaffold. However, a bioactive surface is needed to stimulate implant osteointegration and improve mechanical stability. In this study, porous titanium implants were produced via powder sintering to create different porous diameters and open interconnectivity. Two strategies were used to generate a bioactive surface on the metallic foams: (1) an inorganic alkali thermochemical treatment, (2) grafting a cell adhesive tripeptide (RGD). RGD peptides exhibit an affinity for integrins expressed by osteoblasts, and have been reported to improve osteoblast adhesion, whereas the thermochemical treatment is known to improve titanium implant osseointegration upon implantation. Bioactivated scaffolds and control samples were implanted into the tibiae of rabbits to analyze the effect of these two strategies in vivo regarding bone tissue regeneration through interconnected porosity. Histomorphometric evaluation was performed at 4 and 12 weeks after implantation. Bone-to-implant contact (BIC) and bone in-growth and on-growth were evaluated in different regions of interest (ROIs) inside and outside the implant. The results of this study show that after a long-term postoperative period, the RGD-coated samples presented higher quantification values of quantified newly formed bone tissue in the implant’s outer area. However, the total analyzed bone in-growth was observed to be slightly greater in the scaffolds treated with alkali thermochemical treatment. These results suggest that both strategies contribute to enhancing porous metallic implant stability and osteointegration, and a combination of both strategies might be worth pursuing.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectÀrees temàtiques de la UPC::Enginyeria biomèdica::Biomaterials
dc.subject.otherTitanium foams
dc.subject.otherOsseointegration
dc.subject.otherThermochemical treatment
dc.subject.otherRGD peptide
dc.subject.otherIn vivo implantation
dc.subject.otherHistomorphometric evaluation
dc.subject.otherBone on-growth
dc.subject.otherBone in-growth
dc.titleOn-growth and in-growth osseointegration enhancement in PM porous Ti-scaffolds by two different bioactivation strategies: alkali thermochemical treatment and RGD peptide coating
dc.typeArticle
dc.subject.lemacOsteointegració
dc.contributor.groupUniversitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits
dc.identifier.doi10.3390/ijms23031750
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/3/1750
dc.rights.accessOpen Access
local.identifier.drac32836337
dc.description.versionPostprint (author's final draft)
dc.contributor.covenanteeUniversitat Autònoma de Barcelona
dc.contributor.covenanteeInstitut de Recerca Sant Joan de Déu
dc.contributor.covenanteeAMES
dc.contributor.covenanteeUniversitat de Barcelona
dc.contributor.covenanteeUniversitat Internacional de Catalunya
local.citation.authorKatrin S. Rappe; Ortiz-Hernández, M.; Punset, M.; Molmeneu, M.; Barba, A.; Mas-Moruno, C.; Guillem-Marti, J.; Caparrós, C.; Rupérez de Gracia, E.; Calero, J.; Manzanares, M.; Gil, J.; Franch, J.
local.citation.publicationNameInternational journal of molecular sciences
local.citation.volume23
local.citation.number1750


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