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A tumor-targeted polymer theranostics platform for positron emission tomography and fluorescence imaging
E Koziolova, S Goel, P Chytil, O Janouskova, TE Barnhart, W Cai, T Etrych
Jazyk angličtina Země Velká Británie
Grantová podpora
NV16-28594A
MZ0
CEP - Centrální evidence projektů
PubMed
28731080
DOI
10.1039/c7nr03306k
Knihovny.cz E-zdroje
- MeSH
- doxorubicin aplikace a dávkování farmakokinetika MeSH
- experimentální nádory * diagnostické zobrazování farmakoterapie MeSH
- Jurkat buňky MeSH
- lidé MeSH
- MFC-7 buňky MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- nosiče léků * chemie MeSH
- optické zobrazování * MeSH
- polymery * chemie MeSH
- pozitronová emisní tomografie * MeSH
- radionuklidy MeSH
- teranostická nanomedicína * MeSH
- tkáňová distribuce MeSH
- zirkonium MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
Citace poskytuje Crossref.org
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- $a Koziolova E $u Koziolova, Eva. Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky Sq. 2, Prague 6, 162 06, Czech Republic. etrych@imc.cas.cz.
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- $a A tumor-targeted polymer theranostics platform for positron emission tomography and fluorescence imaging / $c E Koziolova, S Goel, P Chytil, O Janouskova, TE Barnhart, W Cai, T Etrych
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- $a Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on <ovid:sup>89</ovid:sup>Zr-labeled N-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were designed and synthesized and their biodistribution in vivo was successfully and precisely observed over 72 h. Moreover, the feasibility of two imaging techniques, fluorescence imaging (FI) and positron emission tomography (PET), was compared using labeled polymer conjugates. Both methods gave comparable results thus showing the enhanced diagnostic potential of the prepared polymer-dye or polymer-chelator-<ovid:sup>89</ovid:sup>Zr constructs. The in vivo and ex vivo PET/FI studies indicated that the dispersity and molecular weight of the linear HPMA polymers have a significant influence on the pharmacokinetics of the polymer conjugates. The higher molecular weight and narrower distribution of molecular weights of the polymer carriers improve their pharmacokinetic profile for highly prolonged blood circulation and enhanced tumor uptake. Moreover, the same polymer carrier with the anticancer drug doxorubicin bound by a pH-sensitive hydrazone bond showed higher cytotoxicity and cellular uptake in vitro. Therefore, HPMA copolymers with low dispersity and a molecular weight near the limit of renal filtration can be used as highly efficient polymer carriers of tumor-targeted therapeutics or for theranostics with minimal side effects.
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