Bioinspired orthogonal-shaped protein–biometal nanocrystals enable oral protein absorption
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicas (CiMUS) | |
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Fisioloxía | |
| dc.contributor.author | Durán Lobato, Matilde | |
| dc.contributor.author | Tovar Carro, Sulay A. | |
| dc.contributor.author | Cuñarro, Juan | |
| dc.contributor.author | Chenlo Miranda, Miguel Ángel | |
| dc.contributor.author | Álvarez Villamarín, María Clara | |
| dc.contributor.author | Alonso Fernández, María José | |
| dc.date.accessioned | 2025-07-02T11:05:04Z | |
| dc.date.available | 2025-07-02T11:05:04Z | |
| dc.date.issued | 2024-11-17 | |
| dc.description.abstract | With the growing number of marketed biological drugs, the development of technological strategies for their oral systemic absorption, becomes increasingly important. The harsh gastrointestinal environment and low permeability of the intestinal epithelium, represent a huge challenge for their systemic delivery. Herein, bioinspired in the physiological insulin-Zn interaction, the design of orthogonal-shaped protein-biometal hybrid nanocrystals, further enveloped by a bilayer of functional biomaterials, is reported. The nanocrystals exhibited a size of 80 nm, a neutral surface charge and a high insulin loading. In vitro studies showed the capacity of the nanocomplexes to control the release of the associated insulin, while preserving its stability. In vivo evaluation showed sustained blood glucose reductions in both healthy and diabetic rats (up to 40 % and 80 %, respectively), while chronic immunotoxicity studies in mice indicated no toxicity effect. Preliminary efficacy studies in healthy awake pigs following oral capsule administration showed over 20 % absolute bioavailability. | |
| dc.description.peerreviewed | SI | |
| dc.description.sponsorship | This work was supported by the European TRANS-INT Consortium, which received funding from the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement NO. 281035. M. Duran-Lobato' acknowledges a postdoctoral fellowship (Contrato de Acceso al Sistema Espanol ˜ de Ciencia, Tecnología e Innovacion ´ (grant number USE-19533-Y)) granted by “VI Plan Propio” from the University of Seville. | |
| dc.identifier.citation | Matilde Durán-Lobato, Sulay Tovar, Juan Cuñarro, Rocío Ramos-Membrive, Iván Peñuelas, Ilaria Marigo, Federico Benetti, Miguel Chenlo, Clara V. Álvarez, Vashegyi Ildikó, Rudolf Urbanics, János Szebeni, María José Alonso, Bioinspired orthogonal-shaped protein–biometal nanocrystals enable oral protein absorption, Journal of Controlled Release, Volume 377, 2025, Pages 17-36, ISSN 0168-3659, https://doi.org/10.1016/j.jconrel.2024.11.016 | |
| dc.identifier.doi | 10.1016/j.jconrel.2024.11.016 | |
| dc.identifier.issn | 0168-3659 | |
| dc.identifier.uri | https://hdl.handle.net/10347/42376 | |
| dc.journal.title | Journal of Controlled Release | |
| dc.language.iso | eng | |
| dc.page.final | 36 | |
| dc.page.initial | 17 | |
| dc.publisher | Elsevier | |
| dc.relation.publisherversion | https://doi.org/10.1016/j.jconrel.2024.11.016 | |
| dc.rights | © 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license. Attribution-NonCommercial-NoDerivatives 4.0 International | |
| dc.rights.accessRights | open access | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.subject | Peptide delivery | |
| dc.subject | Protein delivery | |
| dc.subject | Oral delivery | |
| dc.subject | Transmucosal | |
| dc.subject | Biologicals | |
| dc.subject | Nanocomplexes | |
| dc.title | Bioinspired orthogonal-shaped protein–biometal nanocrystals enable oral protein absorption | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dc.volume.number | 377 | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 5740f5b3-5af4-4a61-9d24-c8b9d0508177 | |
| relation.isAuthorOfPublication | 501409ac-b47a-41e2-b30c-8692fa1e5307 | |
| relation.isAuthorOfPublication | 7bcdc357-e1b8-4198-b799-86057649f479 | |
| relation.isAuthorOfPublication.latestForDiscovery | 5740f5b3-5af4-4a61-9d24-c8b9d0508177 |
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