Gadolinium- and manganite-based contrast agents with fluorescent probes for both magnetic resonance and fluorescence imaging of pancreatic islets: a comparative study
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
23316021
DOI
10.1002/cmdc.201200439
Knihovny.cz E-zdroje
- MeSH
- beta-cyklodextriny chemie MeSH
- fluorescenční barviva chemie MeSH
- fluorescenční mikroskopie MeSH
- gadolinium chemie MeSH
- kontrastní látky chemie MeSH
- kovové nanočástice chemie MeSH
- krysa rodu Rattus MeSH
- kultivované buňky MeSH
- Langerhansovy ostrůvky cytologie diagnostické zobrazování metabolismus MeSH
- magnetická rezonanční tomografie MeSH
- potkani inbrední LEW MeSH
- radiografie MeSH
- sloučeniny manganu chemie MeSH
- titan chemie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- beta-cyklodextriny MeSH
- betadex MeSH Prohlížeč
- fluorescenční barviva MeSH
- gadolinium MeSH
- kontrastní látky MeSH
- manganite MeSH Prohlížeč
- sloučeniny manganu MeSH
- titan MeSH
- titanium dioxide MeSH Prohlížeč
Three magnetic resonance (MR)/fluorescence imaging probes were tested for visualization, cellular distribution, and survival of labeled pancreatic islets in vitro and following transplantation. As T(1) contrast agents (CAs), gadolinium(III) complexes linked to β-cyclodextrin (Gd-F-βCD) or bound to titanium dioxide (TiO2 @RhdGd) were tested. As a T(2) CA, perovskite manganite nanoparticles (LSMO@siF@si) were examined. Fluorescein or rhodamine was incorporated as a fluorescent marker in all probes. Islets labeled with gadolinium(III) CAs were visible as hyperintense spots on MR in vitro, but detection in vivo was inconclusive. Islets labeled with LSMO@siF@si CA were clearly visible as hypointense spots or areas on MR scans in vitro as well as in vivo. All CAs were detected inside the islet cells by fluorescence. Although the vitality and function of the labeled islets was not impaired by any of the tested CAs, results indicate that LSMO@siF@si CA is a superior marker for islet labeling, as it provides better contrast enhancement within a shorter scan time.
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