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Determination of the Elution Capacity of Dalbavancin in Bone Cements: New Alternative for the Treatment of Biofilm-Related Peri-Prosthetic Joint Infections Based on an In Vitro Study

dc.contributor.authorSánchez Somolinos, M.
dc.contributor.authorDiez Navarro, Marta
dc.contributor.authorBenjumea, Antonio
dc.contributor.authorTormo, Marta
dc.contributor.authorMatas, José
dc.contributor.authorVaquero, Javier
dc.contributor.authorMuñoz, Patricia
dc.contributor.authorMuñoz García, Patricia Carmen
dc.contributor.authorSanz Ruiz, Pablo
dc.contributor.authorGuembe, Maria
dc.date.accessioned2025-02-01T22:31:24Z
dc.date.available2025-02-01T22:31:24Z
dc.date.issued2022-09-13
dc.description.abstractAntibiotic-loaded bone cement is the most widely used approach for the treatment of biofilm-induced septic sequelae in orthopedic surgery. Dalbavancin is a lipoglycopeptide that acts against Gram-positive bacteria and has a long half-life, so we aimed to assess whether it could be a new alternative drug in antibiotic-loaded bone cement for the treatment of periprosthetic joint infections. We assessed the elution capacity of dalbavancin and compared it with that of vancomycin in bone cement. Palacos®R (Heraeus Medical GmbH, Wehrheim, Germany) bone cement was manually mixed with each of the antibiotics studied at 2.5% and 5%. Three cylinders were obtained from each of the mixtures; these were weighed and incubated in 5 mL phosphate-buffered saline at 37°C under shaking for 1 h, 2 h, 4 h, 8 h, 24 h, 48 h, 168 h, and 336 h. PBS was replenished at each time point. The samples were analyzed using high-performance liquid chromatography (vancomycin) and mass cytometry (dalbavancin). Elution was higher than the minimum inhibitory concentration (MIC)90 for both antibiotics after 14 days of study. The release of vancomycin at 14 days was higher than of dalbavancin at each concentration tested (p = 0.05, both). However, the cumulative release of 5% dalbavancin was similar to that of 2.5% vancomycin (p = 0.513). The elution capacity of dalbavancin reached a cumulative concentration similar to that of vancomycin. Moreover, considering that the MIC90 of dalbavancin is one third that of vancomycin (0.06 mg/L and 2 mg/L, respectively) and given the long half-life of dalbavancin, it may be a new alternative for the treatment of biofilm-related periprosthetic infections when loaded in bone cement.
dc.description.departmentDepto. de Cirugía
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationSánchez-Somolinos, M., Díaz-Navarro, M., Benjumea, A., Tormo, M., Matas, J., Vaquero, J., Muñoz, P., Sanz-Ruíz, P., & Guembe, M. (2022). Determination of the elution capacity of dalbavancin in bone cements: New alternative for the treatment of biofilm-related peri-prosthetic joint infections based on an in vitro study. Antibiotics, 11(10), 1300. https://doi.org/10.3390/antibiotics11101300
dc.identifier.doi10.3390/antibiotics11101300
dc.identifier.officialurlhttps://doi.org/10.3390/ANTIBIOTICS11101300
dc.identifier.relatedurlhttps://www.mdpi.com/2079-6382/11/10/1300
dc.identifier.urihttps://hdl.handle.net/20.500.14352/117533
dc.issue.number10
dc.journal.titleAntibiotics
dc.language.isoeng
dc.publisherMDPI
dc.rights.accessRightsopen access
dc.subject.keywordDalbavancin
dc.subject.keywordBone cement
dc.subject.keywordPolymethylmethacrylate
dc.subject.keywordElution
dc.subject.keywordCumulative concentration
dc.subject.keywordVancomycin
dc.subject.ucmSistema musculoesquelético
dc.subject.unesco3213.10 Cirugía Ortopédica
dc.titleDetermination of the Elution Capacity of Dalbavancin in Bone Cements: New Alternative for the Treatment of Biofilm-Related Peri-Prosthetic Joint Infections Based on an In Vitro Study
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication
relation.isAuthorOfPublication057f539e-41b0-4a1e-b97b-204a23ead398
relation.isAuthorOfPublication061c75db-fa4f-42b8-a1ed-56af2ec6a137
relation.isAuthorOfPublication061c75db-fa4f-42b8-a1ed-56af2ec6a137
relation.isAuthorOfPublication.latestForDiscovery057f539e-41b0-4a1e-b97b-204a23ead398

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