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dc.contributor.authorDelgado Hernández, Araceli Rita 
dc.contributor.authorGarcía García, Patricia
dc.contributor.authorReyes, Ricardo 
dc.contributor.authorSegredo Morales, Elisabet
dc.contributor.authorPérez Herrero, Edgar
dc.contributor.authorÉvora, Carmen
dc.contributor.otherGrupo de investigación: "Sistemas de Liberación de Fármacos" Instituto de Tecnologías Biomédicas
dc.date.accessioned2024-02-07T21:07:14Z
dc.date.available2024-02-07T21:07:14Z
dc.date.issued2019
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/36138
dc.description.abstractThe controlled release of active substances—bone morphogenetic protein 2 (BMP-2) and 17β-estradiol—is one of the main aspects to be taken into account to successfully regenerate a tissue defect. In this study, BMP-2- and 17β-estradiol-loaded microspheres were combined in a sandwich-like system formed by a hydrogel core composed of chitosan (CHT) collagen, 2-hidroxipropil γ-ciclodextrin (HP-γ-CD), nanoparticles of hydroxyapatite (nano-HAP), and an electrospun mesh shell prepared with two external electrospinning films for the regeneration of a critical bone defect in osteoporotic rats. Microspheres were made with poly-lactide-co-glycolide (PLGA) to encapsulate BMP-2, whereas the different formulations of 17β-estradiol were prepared with poly-lactic acid (PLA) and PLGA. The in vitro and in vivo BMP-2 delivered from the system fitted a biphasic profile. Although the in vivo burst effect was higher than in vitro the second phases (lasted up to 6 weeks) were parallel, the release rate ranged between 55 and 70 ng/day. The in vitro release kinetics of the 17β-estradiol dissolved in the polymeric matrix of the microspheres depended on the partition coefficient. The 17β-estradiol was slowly released from the core system using an aqueous release medium (Deff = 5.58·10−16 ± 9.81·10−17m2 s −1 ) and very fast in MeOH-water (50:50). The hydrogel core system was injectable, and approximately 83% of the loaded dose is uniformly discharged through a 20G needle. The system placed in the defect was easily adapted to the defect shape and after 12 weeks approximately 50% of the defect was refilled by new tissue. None differences were observed between the osteoporotic and non-osteoporotic groups. Despite the role of 17β-estradiol on the bone remodeling process, the obtained results in this study suggest that the observed regeneration was only due to the controlled rate released of BMP-2 from the PLGA microspheres.
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesPharmaceutics 2019, 11, 648
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.titlePLGA-BMP-2 and PLA-17ß-estradiol microspheres reinforcing a composite hydrogel for bone regeneration in osteoporosis
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/pharmaceutics11120648
dc.subject.keywordBMP-2-microspheres
dc.subject.keywordhydrogel system


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