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Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles

The blood–brain barrier (BBB), built by brain endothelial cells (BECs), is impermeable to biologics. Liposomes and other nanoparticles are good candidates for the delivery of biologics across the BECs, as they can encapsulate numerous molecules of interest in an omnipotent manner. The liposomes need...

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Autores principales: Thomsen, Maj Schneider, Johnsen, Kasper Bendix, Kucharz, Krzysztof, Lauritzen, Martin, Moos, Torben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608573/
https://www.ncbi.nlm.nih.gov/pubmed/36297671
http://dx.doi.org/10.3390/pharmaceutics14102237
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author Thomsen, Maj Schneider
Johnsen, Kasper Bendix
Kucharz, Krzysztof
Lauritzen, Martin
Moos, Torben
author_facet Thomsen, Maj Schneider
Johnsen, Kasper Bendix
Kucharz, Krzysztof
Lauritzen, Martin
Moos, Torben
author_sort Thomsen, Maj Schneider
collection PubMed
description The blood–brain barrier (BBB), built by brain endothelial cells (BECs), is impermeable to biologics. Liposomes and other nanoparticles are good candidates for the delivery of biologics across the BECs, as they can encapsulate numerous molecules of interest in an omnipotent manner. The liposomes need attachment of a targeting molecule, as BECs unfortunately are virtually incapable of uptake of non-targeted liposomes from the circulation. Experiments of independent research groups have qualified antibodies targeting the transferrin receptor as superior for targeted delivery of nanoparticles to BECs. Functionalization of nanoparticles via conjugation with anti-transferrin receptor antibodies leads to nanoparticle uptake by endothelial cells of both brain capillaries and post-capillary venules. Reducing the density of transferrin receptor-targeted antibodies conjugated to liposomes limits uptake in BECs. Opposing the transport of nanoparticles conjugated to high-affine anti-transferrin receptor antibodies, lowering the affinity of the targeting antibodies or implementing monovalent antibodies increase uptake by BECs and allows for further transport across the BBB. The novel demonstration of transport of targeted liposomes in post-capillary venules from blood to the brain is interesting and clearly warrants further mechanistic pursuit. The recent evidence for passing targeted nanoparticles through the BBB shows great promise for future drug delivery of biologics to the brain.
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spelling pubmed-96085732022-10-28 Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles Thomsen, Maj Schneider Johnsen, Kasper Bendix Kucharz, Krzysztof Lauritzen, Martin Moos, Torben Pharmaceutics Review The blood–brain barrier (BBB), built by brain endothelial cells (BECs), is impermeable to biologics. Liposomes and other nanoparticles are good candidates for the delivery of biologics across the BECs, as they can encapsulate numerous molecules of interest in an omnipotent manner. The liposomes need attachment of a targeting molecule, as BECs unfortunately are virtually incapable of uptake of non-targeted liposomes from the circulation. Experiments of independent research groups have qualified antibodies targeting the transferrin receptor as superior for targeted delivery of nanoparticles to BECs. Functionalization of nanoparticles via conjugation with anti-transferrin receptor antibodies leads to nanoparticle uptake by endothelial cells of both brain capillaries and post-capillary venules. Reducing the density of transferrin receptor-targeted antibodies conjugated to liposomes limits uptake in BECs. Opposing the transport of nanoparticles conjugated to high-affine anti-transferrin receptor antibodies, lowering the affinity of the targeting antibodies or implementing monovalent antibodies increase uptake by BECs and allows for further transport across the BBB. The novel demonstration of transport of targeted liposomes in post-capillary venules from blood to the brain is interesting and clearly warrants further mechanistic pursuit. The recent evidence for passing targeted nanoparticles through the BBB shows great promise for future drug delivery of biologics to the brain. MDPI 2022-10-19 /pmc/articles/PMC9608573/ /pubmed/36297671 http://dx.doi.org/10.3390/pharmaceutics14102237 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Thomsen, Maj Schneider
Johnsen, Kasper Bendix
Kucharz, Krzysztof
Lauritzen, Martin
Moos, Torben
Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title_full Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title_fullStr Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title_full_unstemmed Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title_short Blood–Brain Barrier Transport of Transferrin Receptor-Targeted Nanoparticles
title_sort blood–brain barrier transport of transferrin receptor-targeted nanoparticles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608573/
https://www.ncbi.nlm.nih.gov/pubmed/36297671
http://dx.doi.org/10.3390/pharmaceutics14102237
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