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dc.contributorUniversitat Ramon Llull. IQS
dc.contributor.authorPrades, Roger
dc.contributor.authorTeixidó, Meritxell
dc.contributor.authorOller-Salvia, Benjamí
dc.date.accessioned2025-04-30T12:54:21Z
dc.date.issued2025-03-03
dc.identifier.issn1543-8392ca
dc.identifier.urihttp://hdl.handle.net/20.500.14342/5250
dc.description.abstractThe pharmacological treatment of central nervous system diseases faces significant challenges due to the presence of the blood–brain barrier (BBB). This barrier naturally protects the brain and prevents therapeutics from reaching their targets efficiently. However, the BBB allows the passage of nutrients and other molecules that guarantee brain homeostasis through selective transport mechanisms present at the BBB. These mechanisms provide an opportunity for delivering therapeutic agents into the central nervous system using brain shuttles. Here we review the progress of brain shuttle peptide development from 2015 until 2025. We highlight the most utilized peptides and describe trends in strategies to develop new shuttles and enhance their transport efficiency. Additionally, we compared them with other types of brain shuttles and emphasize the progress of peptide shuttles toward clinical translation.ca
dc.format.extentp.10ca
dc.language.isoengca
dc.publisherAmerican Chemical Societyca
dc.relation.ispartofMolecular Pharmaceutics 2025, 22, 3, 1100–1109ca
dc.rights© L'autor/aca
dc.subject.otherBlood-brain barrierca
dc.subject.otherBrain shuttleca
dc.subject.otherDrug deliveryca
dc.subject.otherPeptide shuttleca
dc.subject.otherCentral nervous system therapeuticsca
dc.subject.otherBarrera hematoencefàlicaca
dc.subject.otherMedicaments--Modes d'administracióca
dc.subject.otherSistema nerviós central--Tractamentca
dc.titleNew Trends in Brain Shuttle Peptidesca
dc.typeinfo:eu-repo/semantics/articleca
dc.rights.accessLevelinfo:eu-repo/semantics/embargoedAccess
dc.date.embargoEnd2026-03-03T01:00:00Z
dc.embargo.terms12 mesosca
dc.subject.udc615ca
dc.subject.udc616.1ca
dc.identifier.doihttps://doi.org/10.1021/acs.molpharmaceut.4c01327ca
dc.relation.projectIDinfo:eu-repo/grantAgreement/MCIU/PN I+D/PID2023-151988OB-I00ca
dc.description.versioninfo:eu-repo/semantics/acceptedVersionca


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