Viral protein nanoparticles (Part 1): Pharmaceutical characteristics

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicas (CiMUS)
dc.contributor.authorMellid Carballal, Rocío
dc.contributor.authorGutiérrez Gutiérrez, Sara
dc.contributor.authorRivas, Carmen
dc.contributor.authorGarcía Fuentes, Marcos
dc.date.accessioned2025-09-25T11:44:07Z
dc.date.available2025-09-25T11:44:07Z
dc.date.issued2023-08
dc.description.abstractViral protein nanoparticles fill the gap between viruses and synthetic nanoparticles. Combining advantageous properties of both systems, they have revolutionized pharmaceutical research. Virus-like particles are characterized by a structure identical to viruses but lacking genetic material. Another type of viral protein nanoparticles, virosomes, are similar to liposomes but include viral spike proteins. Both systems are effective and safe vaccine candidates capable of overcoming the disadvantages of both traditional and subunit vaccines. Besides, their particulate structure, biocompatibility, and biodegradability make them good candidates as vectors for drug and gene delivery, and for diagnostic applications. In this review, we analyze viral protein nanoparticles from a pharmaceutical perspective and examine current research focused on their development process, from production to administration. Advances in synthesis, modification and formulation of viral protein nanoparticles are critical so that large-scale production of viral protein nanoparticle products becomes viable and affordable, which ultimately will increase their market penetration in the future. We will discuss their expression systems, modification strategies, formulation, biopharmaceutical properties, and biocompatibility.
dc.description.peerreviewedSI
dc.description.sponsorshipThis publication is part of the following grants: PID2021–124986OB-I00 (Project “IMMMA”) funded by MCIN/AEI/ 10.13039/501100011033 and by “ERDF A way of making Europe”; AC21_2/00046 (Project “RAIN”) funded by Health Institute Carlos III/MCIN/AEI/ 10.13039/501100011033 and by “European Union NextGenerationEU/EURONANOMED 3. Funding at the laboratory of CR is provided by PID2021–126510NB-I00 funded by MCIN/AEI/10.13039/501100011033 and FEDER (a way to build Europe), and by Xunta de Galicia (ED431G 2019/02). RMC is a recipient of a predoctoral grant from the Ministerio de Educación y Formación Profesional (FPU20/01525).
dc.identifier.doi10.1016/j.ejps.2023.106460
dc.identifier.issn0928-0987
dc.identifier.urihttps://hdl.handle.net/10347/42904
dc.issue.number106460
dc.journal.titleEuropean Journal of Pharmaceutical Sciences
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-124986OB-I00/ES/MATRICES MIMETIZANTES DE LA INFECCION/
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 (ISCIII)/AC21_2%2F00046/ES/NICHOS INMUNOMODULATORIOS RADIO-ACTIVADOS/
dc.relation.publisherversionhttps://doi.org/10.1016/j.ejps.2023.106460
dc.relation.publisherversionhttps://doi.org/10.1016/j.ejps.2023.106460
dc.rights© 2023 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). Attribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleViral protein nanoparticles (Part 1): Pharmaceutical characteristics
dc.typejournal article
dc.volume.number187
dspace.entity.typePublication
relation.isAuthorOfPublication186becc2-6335-4e40-9df7-17f63a37d9d2
relation.isAuthorOfPublication.latestForDiscovery186becc2-6335-4e40-9df7-17f63a37d9d2

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