Self-assembled fluorinated nanoparticles as sensitive and biocompatible theranostic platforms for 19F MRI
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F24%3A00084916" target="_blank" >RIV/00023001:_____/24:00084916 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11310/24:10477853 RIV/46747885:24530/24:00013002 RIV/00216208:11110/24:10477853
Výsledek na webu
<a href="https://onlinelibrary.wiley.com/doi/epdf/10.1002/mabi.202300510" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1002/mabi.202300510</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/mabi.202300510" target="_blank" >10.1002/mabi.202300510</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Self-assembled fluorinated nanoparticles as sensitive and biocompatible theranostic platforms for 19F MRI
Popis výsledku v původním jazyce
Theranostics is a novel paradigm integrating therapy and diagnostics, thereby providing new prospects for overcoming the limitations of traditional treatments. In this context, perfluorocarbons (PFCs) are the most widely used tracers in preclinical fluorine-19 magnetic resonance (F-19 MR), primarily for their high fluorine content. However, PFCs are extremely hydrophobic, and their solutions often display reduced biocompatibility, relative instability, and subpar F-19 MR relaxation times. This study aims to explore the potential of micellar F-19 MR imaging (MRI) tracers, synthesized by polymerization-induced self-assembly (PISA), as alternative theranostic agents for simultaneous imaging and release of the non-steroidal antileprotic drug clofazimine. In vitro, under physiological conditions, these micelles demonstrate sustained drug release. In vivo, throughout the drug release process, they provide a highly specific and sensitive F-19 MRI signal. Even after extended exposure, these fluoropolymer tracers show biocompatibility, as confirmed by the histological analysis. Moreover, the characteristics of these polymers can be broadly adjusted by design to meet the wide range of criteria for preclinical and clinical settings. Therefore, micellar 19F MRI tracers display physicochemical properties suitable for in vivo imaging, such as relaxation times and non-toxicity, and high performance as drug carriers, highlighting their potential as both diagnostic and therapeutic tools.
Název v anglickém jazyce
Self-assembled fluorinated nanoparticles as sensitive and biocompatible theranostic platforms for 19F MRI
Popis výsledku anglicky
Theranostics is a novel paradigm integrating therapy and diagnostics, thereby providing new prospects for overcoming the limitations of traditional treatments. In this context, perfluorocarbons (PFCs) are the most widely used tracers in preclinical fluorine-19 magnetic resonance (F-19 MR), primarily for their high fluorine content. However, PFCs are extremely hydrophobic, and their solutions often display reduced biocompatibility, relative instability, and subpar F-19 MR relaxation times. This study aims to explore the potential of micellar F-19 MR imaging (MRI) tracers, synthesized by polymerization-induced self-assembly (PISA), as alternative theranostic agents for simultaneous imaging and release of the non-steroidal antileprotic drug clofazimine. In vitro, under physiological conditions, these micelles demonstrate sustained drug release. In vivo, throughout the drug release process, they provide a highly specific and sensitive F-19 MRI signal. Even after extended exposure, these fluoropolymer tracers show biocompatibility, as confirmed by the histological analysis. Moreover, the characteristics of these polymers can be broadly adjusted by design to meet the wide range of criteria for preclinical and clinical settings. Therefore, micellar 19F MRI tracers display physicochemical properties suitable for in vivo imaging, such as relaxation times and non-toxicity, and high performance as drug carriers, highlighting their potential as both diagnostic and therapeutic tools.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10404 - Polymer science
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Macromolecular bioscience
ISSN
1616-5187
e-ISSN
1616-5195
Svazek periodika
24
Číslo periodika v rámci svazku
6
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
9
Strana od-do
"art. no. 2300510"
Kód UT WoS článku
001144788700001
EID výsledku v databázi Scopus
2-s2.0-85182454477