Rodyti trumpą aprašą

dc.contributor.authorKlimkevičius, Vaidas
dc.contributor.authorVoronovič, Evelina
dc.contributor.authorJarockytė, Greta
dc.contributor.authorSkripka, Artiom
dc.contributor.authorVetrone, Fiorenzo
dc.contributor.authorRotomskis, Ričardas
dc.contributor.authorKatelnikovas, Artūras
dc.contributor.authorKarabanovas, Vitalijus
dc.date.accessioned2023-09-18T16:16:42Z
dc.date.available2023-09-18T16:16:42Z
dc.date.issued2022
dc.identifier.issn2050-750X
dc.identifier.other(WOS_ID)000739588200001
dc.identifier.urihttps://etalpykla.vilniustech.lt/handle/123456789/112578
dc.description.abstractUpconverting nanoparticles (UCNPs) possess great potential for biomedical application. UCNPs absorb and convert near-infrared (NIR) radiation in the biological imaging window to visible (Vis) and even ultraviolet (UV) radiation. NIR excitation offers reduced scattering and diminished autofluorescence in biological samples, whereas the emitted UV-Vis and NIR photons can be used for cancer treatment and imaging, respectively. However, UCNPs are usually synthesized in organic solvents and are not readily suitable for biomedical application due to the hydrophobic nature of their surface. Herein, we have removed the hydrophobic ligands from the synthesized UCNPs and coated the bare UCNPs with two custom-made hydrophilic polyelectrolytes (synthesized via the reversible addition–fragmentation chain transfer (RAFT) polymerization method). Polymers containing different amounts of PEGylated and carboxylic groups were studied. Coating with both polymers increased the upconversion (UC) emission intensity and photoluminescence lifetime values of the UCNPs, which directly translates to more efficient cancer cell labeling nanoprobes. The polymer composition plays a crucial role in the modification of UCNPs, not only with respect to their colloidal stability, but also with respect to the cellular uptake. Colloidally unstable bare UCNPs aggregate in cell culture media and precipitate, rendering themselves unsuitable for any biomedical use. However, stabilization with polymers prevents UCNPs from aggregation, increases their uptake in cells, and improves the quality of cellular labeling. This investigation sheds light on the appropriate coating for UCNPs and provides relevant insights for the rational development of imaging and therapeutic tools.eng
dc.formatPDF
dc.format.extentp. 625-636
dc.format.mediumtekstas / txt
dc.language.isoeng
dc.relation.isreferencedbyScience Citation Index Expanded (Web of Science)
dc.relation.isreferencedbyScopus
dc.rightsNeprieinamas
dc.titlePolymer brush coated upconverting nanoparticles with improved colloidal stability and cellular labeling
dc.typeStraipsnis Web of Science DB / Article in Web of Science DB
dcterms.references81
dc.type.pubtypeS1 - Straipsnis Web of Science DB / Web of Science DB article
dc.contributor.institutionVilniaus universitetas
dc.contributor.institutionNacionalinis vėžio institutas Vilniaus Gedimino technikos universitetas Vilniaus universitetas
dc.contributor.institutionNacionalinis vėžio institutas Vilniaus universitetas
dc.contributor.institutionUniversité du Québec
dc.contributor.institutionNacionalinis vėžio institutas Vilniaus Gedimino technikos universitetas
dc.contributor.facultyFundamentinių mokslų fakultetas / Faculty of Fundamental Sciences
dc.subject.researchfieldN 011 - Biofizika / Biophysics
dc.subject.researchfieldN 003 - Chemija / Chemistry
dc.subject.researchfieldT 005 - Chemijos inžinerija / Chemical engineering
dc.subject.researchfieldT 008 - Medžiagų inžinerija / Material engineering
dc.subject.vgtuprioritizedfieldsFM0202 - Ląstelių ir jų biologiškai aktyvių komponentų tyrimai / Investigations on cells and their biologically active components
dc.subject.ltspecializationsL105 - Sveikatos technologijos ir biotechnologijos / Health technologies and biotechnologies
dcterms.sourcetitleJournal of materials chemistry B
dc.description.issueiss. 4
dc.description.volumevol. 10
dc.publisher.nameRoyal Society of Chemistry
dc.publisher.cityCambridge
dc.identifier.doi000739588200001
dc.identifier.doi132860578
dc.identifier.doi10.1039/d1tb01644j
dc.identifier.elaba116886051


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