Peptide ligands on the PEGylated nanoparticle surface and human serum composition are key factors for the interaction between immune cells and nanoparticles

Bibliographische Detailangaben
Parent link:Colloids and Surfaces B: Biointerfaces
Vol. 221.— 2023.— [112981, 13 p.]
Körperschaft: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Weitere Verfasser: Pershina A. G. Aleksandra Gennadievna, Demin A. M., Perekucha N. A. Nataljya Andreevna, Brikunova O. Ya. Olga Yaroslavovna, Efimova L. V. Lina Viktorovna, Nevskaya K. V., Vakhrushev A. V. Aleksandr, Zgoda V. G. Viktor, Uymin M. A. Mikhail Aleksandrovich, Minin A. S. Artyom, Malkeeva D. Dina, Kiseleva E. Elena, Zima A. P. Anastasiya Pavlovna, Krasnov V. P. Viktor, Ogorodova L. M. Lyudmila Mikhaylovna
Zusammenfassung:Title screen
The architecture of a nanoparticles’ surface formed due to a modification with a ligand and protein corona formation in biofluids is critical for interactions with cells in vivo. Here we studied interactions of immune cells with magnetic nanoparticles (MNPs) covalently modified with polyethylene glycol (PEG) and their counterparts conjugated with peptides: a pH (low) insertion peptide (pHLIP) and cycloRGD as a targeting ligand in human serum. The conjugation of MNPs-PEG with pHLIP, but not with cycloRGD, enhanced the association of these particles with mononuclear phagocytic cells in vitro and in vivo. We did not find a clear difference in protein corona composition between the pHLIP-modified and parental PEGylated nanoparticles. Analysis of the effect of autologous human serum on MNP uptake by monocytes showed that the efficiency of endocytosis varies among healthy donors and depends on intrinsic properties of serum. Nevertheless, using classic blood, coagulation, biochemical tests, and anti-PEG IgG serum level, we failed to identify the cause of the observed interdonor variation. These individual differences should be taken into consideration during testing of nanotherapeutics.
Режим доступа: по договору с организацией-держателем ресурса
Sprache:Englisch
Veröffentlicht: 2023
Schlagworte:
Online-Zugang:https://doi.org/10.1016/j.colsurfb.2022.112981
Format: Elektronisch Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=669441

MARC

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200 1 |a Peptide ligands on the PEGylated nanoparticle surface and human serum composition are key factors for the interaction between immune cells and nanoparticles  |f A. G. Pershina, A. M. Demin, N. A. Perekucha [et al.] 
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330 |a The architecture of a nanoparticles’ surface formed due to a modification with a ligand and protein corona formation in biofluids is critical for interactions with cells in vivo. Here we studied interactions of immune cells with magnetic nanoparticles (MNPs) covalently modified with polyethylene glycol (PEG) and their counterparts conjugated with peptides: a pH (low) insertion peptide (pHLIP) and cycloRGD as a targeting ligand in human serum. The conjugation of MNPs-PEG with pHLIP, but not with cycloRGD, enhanced the association of these particles with mononuclear phagocytic cells in vitro and in vivo. We did not find a clear difference in protein corona composition between the pHLIP-modified and parental PEGylated nanoparticles. Analysis of the effect of autologous human serum on MNP uptake by monocytes showed that the efficiency of endocytosis varies among healthy donors and depends on intrinsic properties of serum. Nevertheless, using classic blood, coagulation, biochemical tests, and anti-PEG IgG serum level, we failed to identify the cause of the observed interdonor variation. These individual differences should be taken into consideration during testing of nanotherapeutics. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Colloids and Surfaces B: Biointerfaces 
463 |t Vol. 221  |v [112981, 13 p.]  |d 2023 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a immune cells 
701 1 |a Pershina  |b A. G.  |c biologist  |c Associate Professor of Tomsk Polytechnic University, Candidate of biological sciences  |f 1981-  |g Aleksandra Gennadievna  |3 (RuTPU)RU\TPU\pers\32466  |9 16414 
701 1 |a Demin  |b A. M. 
701 1 |a Perekucha  |b N. A.  |g Nataljya Andreevna 
701 1 |a Brikunova  |b O. Ya.  |g Olga Yaroslavovna 
701 1 |a Efimova  |b L. V.  |g Lina Viktorovna 
701 1 |a Nevskaya  |b K. V. 
701 1 |a Vakhrushev  |b A. V.  |g Aleksandr 
701 1 |a Zgoda  |b V. G.  |g Viktor 
701 1 |a Uymin  |b M. A.  |g Mikhail Aleksandrovich 
701 1 |a Minin  |b A. S.  |g Artyom 
701 1 |a Malkeeva  |b D.  |g Dina 
701 1 |a Kiseleva  |b E.  |g Elena 
701 1 |a Zima  |b A. P.  |g Anastasiya Pavlovna 
701 1 |a Krasnov  |b V. P.  |g Viktor 
701 1 |a Ogorodova  |b L. M.  |g Lyudmila Mikhaylovna 
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