Publication: Nanoparticle-based drug delivery: Via RBC-hitchhiking for the inhibition of lung metastases growth
dc.contributor.author | Yaremenko, A. V. | |
dc.contributor.author | Babenyshev, A. V. | |
dc.contributor.author | Balalaeva, I. V. | |
dc.contributor.author | Nikitin, M. P. | |
dc.contributor.author | Zelepukin, I. V. | |
dc.contributor.author | Shipunova, V. O. | |
dc.contributor.author | Nikitin, P. I. | |
dc.contributor.author | Deyev, S. M. | |
dc.contributor.author | Никитин, Петр Иванович | |
dc.contributor.author | Деев, Сергей Михайлович | |
dc.date.accessioned | 2024-11-20T09:21:32Z | |
dc.date.available | 2024-11-20T09:21:32Z | |
dc.date.issued | 2019 | |
dc.description.abstract | © The Royal Society of Chemistry. Delivery of particle-based theranostic agents via their transportation on the surfaces of red blood cells, commonly referred to as RBC-hitchhiking, has historically been developed as a promising strategy for increasing the extremely poor blood circulation lifetime, primarily, of the large-sized sub-micron agents. Here, we show for the first time that RBC-hitchhiking can be extremely efficient for nanoparticle delivery and tumor treatment even in those cases when no circulation prolongation is observed. Specifically, we demonstrate that RBC-hitchhiking of certain small 100 nm particles, unlike that of the conventional sub-micron ones, can boost the delivery of non-targeted particles to lungs up to a record high value of 120-fold (and up to 40% of the injected dose). To achieve this remarkable result, we screened sub-200 nm nanoparticles of different sizes, polymer coatings and ζ-potentials and identified particles with the optimal RBC adsorption/desorption behavior. Furthermore, we demonstrated that such RBC-mediated rerouting of particles to lungs can be used to fight pulmonary metastases of aggressive melanoma B16-F1. Our findings could change the general paradigm of drug delivery for cancer treatment with RBC-hitchhiking. It is not the blood circulation lifetime that is the key factor for nanoparticle efficiency, but rather the complexation of nanoparticles with the RBC. The demonstrated technology could become a valuable tool for development of new strategies based on small nanoparticles for the treatment of aggressive and small-cell types of cancer as well as other lung diseases. | |
dc.format.extent | С. 1636-1646 | |
dc.identifier.citation | Nanoparticle-based drug delivery: Via RBC-hitchhiking for the inhibition of lung metastases growth / Yaremenko, A.V. [et al.] // Nanoscale. - 2019. - 11. - № 4. - P. 1636-1646. - 10.1039/c8nr07730d | |
dc.identifier.doi | 10.1039/c8nr07730d | |
dc.identifier.uri | https://www.doi.org/10.1039/c8nr07730d | |
dc.identifier.uri | https://www.scopus.com/record/display.uri?eid=2-s2.0-85060329925&origin=resultslist | |
dc.identifier.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Alerting&SrcApp=Alerting&DestApp=WOS_CPL&DestLinkType=FullRecord&UT=WOS:000459910900013 | |
dc.identifier.uri | https://openrepository.mephi.ru/handle/123456789/16472 | |
dc.relation.ispartof | Nanoscale | |
dc.title | Nanoparticle-based drug delivery: Via RBC-hitchhiking for the inhibition of lung metastases growth | |
dc.type | Article | |
dspace.entity.type | Publication | |
oaire.citation.issue | 4 | |
oaire.citation.volume | 11 | |
relation.isAuthorOfPublication | ba7e8545-c2f2-4ceb-b87c-64517de9a50d | |
relation.isAuthorOfPublication | 66f50b35-0e92-49e0-ad1a-0ac386d858b7 | |
relation.isAuthorOfPublication.latestForDiscovery | ba7e8545-c2f2-4ceb-b87c-64517de9a50d | |
relation.isOrgUnitOfPublication | c8407a6f-7272-450d-8d99-032352c76b55 | |
relation.isOrgUnitOfPublication.latestForDiscovery | c8407a6f-7272-450d-8d99-032352c76b55 |