Nano-bio interaction of magnetic nanoparticles with cells in a tumor at the single-cell level; Nano Today; Vol. 56

Sonraí bibleagrafaíochta
Parent link:Nano Today.— .— Amsterdam: Elsevier Science Publishing Company Inc.
Vol. 56.— 2024.— Article number 102300, 14 p.
Údar corparáideach: Томский политехнический университет (570)
Rannpháirtithe: Pershina A. G. Aleksandra Gennadievna, Efimova L. V. Lina Viktorovna, Brikunova O. Ya. Olga Yaroslavovna, Nevskaya K. V. Ksenia Vladimirovna, Sukhinina E. V. Ekaterina Vladimirovna, Hmelevskaya E. S. Ekaterina Sergeevna, Demin A. M. Aleksandr Mikhaylovich, Naumenko Viktor Alekseevich, Malkeeva D. Dina, Kiseleva E. Elena, Khozyainova A. A. Anna, Menyaylo M. E. Maksim Evgenjevich, Denisov E. V. Evgeny Vladimirovich, Volegov A. S. Aleksey, Uymin M. A. Mikhail Aleksandrovich
Achoimre:Title screen
A benefit of biomedical application of nanosystems is implementation of a precise effect at the level of an individual cell, and magnetic nanoparticles (MNPs) are some of the best candidates for the development of an intelligent nanosystem with remote control. To develop a nanosystem for precise therapy, a deep understanding of the nanosystem’s in vivo behavior is required. Here, we studied penetration and distribution of PEGylated iron oxide MNPs unmodified or modified with the pH low insertion peptide (a ligand for smart targeting of the tumor acidic microenvironment) in vivo in a 4T1 mouse tumor. We revealed that MNPs penetrate into the tumor via both vascular burst and endothelial transcytosis. By implementing an approach based on single-cell high-throughput RNA sequencing, we identified the populations of the cells that took up MNPs in the 4T1 tumor and revealed preferential accumulation of MNPs in regulatory Trem2+ tumor-associated macrophages.
Текстовый файл
AM_Agreement
Teanga:Béarla
Foilsithe / Cruthaithe: 2024
Ábhair:
Rochtain ar líne:https://doi.org/10.1016/j.nantod.2024.102300
Formáid: Leictreonach Caibidil leabhair
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=673572

MARC

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