dc.creator | Formica, María Lina | |
dc.creator | Legeay, Samuel | |
dc.creator | Bejaud, Jérôme | |
dc.creator | Montich, Guillermo Gabriel | |
dc.creator | Ullio Gamboa, Gabriela Veronica | |
dc.creator | Benoit, Jean-Pierre | |
dc.creator | Palma, Santiago Daniel | |
dc.date.accessioned | 2022-08-17T14:31:29Z | |
dc.date.accessioned | 2022-10-15T13:32:10Z | |
dc.date.available | 2022-08-17T14:31:29Z | |
dc.date.available | 2022-10-15T13:32:10Z | |
dc.date.created | 2022-08-17T14:31:29Z | |
dc.date.issued | 2021-02 | |
dc.identifier | Formica, María Lina; Legeay, Samuel; Bejaud, Jérôme; Montich, Guillermo Gabriel; Ullio Gamboa, Gabriela Veronica; et al.; Novel hybrid lipid nanocapsules loaded with a therapeutic monoclonal antibody – Bevacizumab – and Triamcinolone acetonide for combined therapy in neovascular ocular pathologies; Elsevier Science; Materials Science and Engineering: C; 119; 2-2021; 1-10 | |
dc.identifier | 0928-4931 | |
dc.identifier | http://hdl.handle.net/11336/165816 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4391674 | |
dc.description.abstract | The aim of this study was to design and develop a novel hybrid formulation based on lipid nanocapsules containing bevacizumab (BVZ), an effective therapeutic antibody, on the surface and triamcinolone acetonide (TA) in the inner core (BVZ-TA-LNC) intended to improve ocular therapy. Hence, a phase inversion-insertion one step method was developed to drug loading and surface modification of lipid nanocapsules by post-insertion of a bifunctional polymer, followed by antibody coupling using “click” chemistry. The covalent bond and antibody capacity binding to its specific antigen were confirmed by thermal analysis and immunoassay, respectively. BVZ-TA-LNC presented nanometric size (102 nm), negative surface potential (−19 mV) and exhibiting 56% of TA in the lipid core. BVZ-TA-LNC tended to prevent the endothelial cell migration and significantly prevented the capillary formation induced by the vascular endothelium growth factor (VEGF). The novel hybrid system allowed the co-loading of two different therapeutic molecules and may be promising to improve the therapy of eye disorders that occur with inflammation and/or neovascularization. | |
dc.language | eng | |
dc.publisher | Elsevier Science | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0928493120333166?via%3Dihub | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.msec.2020.111398 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | ANTIANGIOGENIC | |
dc.subject | BEVACIZUMAB | |
dc.subject | HYBRID LIPID NANOCAPSULE | |
dc.subject | OPHTHALMIC DRUG DELIVERY | |
dc.subject | THERAPEUTIC ANTIBODY | |
dc.subject | TRIAMCINOLONE ACETONIDE | |
dc.title | Novel hybrid lipid nanocapsules loaded with a therapeutic monoclonal antibody – Bevacizumab – and Triamcinolone acetonide for combined therapy in neovascular ocular pathologies | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:ar-repo/semantics/artículo | |
dc.type | info:eu-repo/semantics/publishedVersion | |