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Osteoporosis Remission and New Bone Formation with Mesoporous Silica Nanoparticles

dc.contributor.authorMora Raimundo, Patricia
dc.contributor.authorLozano Borregón, Daniel
dc.contributor.authorBenito De Las Heras, Manuel R.
dc.contributor.authorMulero, Francisca
dc.contributor.authorManzano García, Miguel
dc.contributor.authorVallet Regí, María Dulce Nombre
dc.date.accessioned2023-06-17T09:05:36Z
dc.date.available2023-06-17T09:05:36Z
dc.date.issued2021-06-06
dc.descriptionRESEARCH ID B-5081-2017  (Daniel Lozano Borregón) ORCID 0000-0001-5902-9201 (Daniel Lozano Borregón) RESEARCH ID K-3719-2014  (Miguel Manzano García) ORCID 0000-0001-6238-6111 (Miguel Manzano García) RESEARCHER ID M-3378-2014 (María Vallet Regí) ORCID 0000-0002-6104-4889 (María Vallet Regí)
dc.description.abstractNanotechnology changed the concept of treatment for a variety of diseases, producing a huge impact regarding drug and gene delivery. Among the different targeted diseases, osteoporosis has devastating clinical and economic consequences. Since current osteoporosis treatments present several side effects, new treatment approaches are needed. Recently, the application of small interfering RNA (siRNA) has become a promising alternative. Wnt/β-catenin signaling pathway controls bone development and formation. This pathway is negatively regulated by sclerostin, which knock-down through siRNA application would potentially promote bone formation. However, the major bottleneck for siRNA-based treatments is the necessity of a delivery vector, bringing nanotechnology as a potential solution. Among the available nanocarriers, mesoporous silica nanoparticles (MSNs) have attracted great attention for intracellular delivery of siRNAs. The mesoporous structure of MSNs permits the delivery of siRNAs together with another biomolecule, achieving a combination therapy. Here, we evaluate the effectiveness of a new potential osteoporosis treatment based on MSNs. Our proposed system was effective in delivering SOST siRNA and osteostatin through systemic injection to bone tissue. The nanoparticle administration produced an increase expression of osteogenic related genes improving the bone microarchitecture. The treated osteoporotic mice recovered values of a healthy situation approaching to osteoporosis remission.en
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.departmentSección Deptal. de Bioquímica y Biología Molecular (Farmacia)
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipUnión Europea
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/65672
dc.identifier.doi10.1002/advs.202101107
dc.identifier.issn2198-3844 (online)
dc.identifier.officialurlhttps://doi.org/10.1002/advs.202101107
dc.identifier.relatedurlhttps://www.ucm.es/valletregigroup
dc.identifier.urihttps://hdl.handle.net/20.500.14352/8151
dc.journal.titleAdvanced Science
dc.language.isoeng
dc.publisherWiley-VCH GmbH
dc.relation.projectIDVERDI (694160)
dc.relation.projectIDPID2019-106436RB-I00
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordOsteoporosis
dc.subject.keywordsiRNAs
dc.subject.keywordCombination therapy
dc.subject.keywordOsteostatin
dc.subject.keywordMesoporous silica nanoparticles
dc.subject.ucmMateriales
dc.subject.unesco3312 Tecnología de Materiales
dc.titleOsteoporosis Remission and New Bone Formation with Mesoporous Silica Nanoparticlesen
dc.typejournal article
dspace.entity.typePublication
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