Modifying the Siderophore Triacetylfusarinine C for Molecular Imaging of Fungal Infection
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
P 25899
Austrian Science Fund FWF - Austria
P 30924
Austrian Science Fund FWF - Austria
PubMed
30838551
PubMed Central
PMC6877352
DOI
10.1007/s11307-019-01325-6
PII: 10.1007/s11307-019-01325-6
Knihovny.cz E-zdroje
- Klíčová slova
- Aspergillus fumigatus, Gallium-68, Infection imaging, PET, Siderophores, Triacetylfusarinine C,
- MeSH
- Aspergillus fumigatus fyziologie MeSH
- krevní proteiny metabolismus MeSH
- krysa rodu Rattus MeSH
- kyseliny hydroxamové chemie MeSH
- lidé MeSH
- molekulární zobrazování * MeSH
- mutace genetika MeSH
- mykózy diagnostické zobrazování mikrobiologie MeSH
- myši inbrední BALB C MeSH
- PET/CT MeSH
- plicní aspergilóza diagnostické zobrazování mikrobiologie MeSH
- radioizotopy galia chemie MeSH
- siderofory chemická syntéza chemie MeSH
- tkáňová distribuce MeSH
- vazba proteinů MeSH
- železité sloučeniny chemie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- Gallium-68 MeSH Prohlížeč
- krevní proteiny MeSH
- kyseliny hydroxamové MeSH
- N,N',N''-triacetylfusarinine C MeSH Prohlížeč
- radioizotopy galia MeSH
- siderofory MeSH
- železité sloučeniny MeSH
PURPOSE: Aspergillus fumigatus produces the siderophore triacetylfusarinine C (TAFC) for iron acquisition which is essential for its virulence. Therefore, TAFC is a specific marker for invasive aspergillosis. We have shown previously that positron emission tomography (PET) imaging with [68Ga]TAFC exhibited excellent targeting properties in an A. fumigatus rat infection model. In this study, we aimed to prepare TAFC analogs modifying fusarinine C (FSC) by acylation with different carbon chain lengths as well as with charged substituents and investigated the influence of introduced substituents on preservation of TAFC characteristics in vitro and in vivo. PROCEDURES: Fifteen TAFC derivatives were prepared and labeled with gallium-68. In vitro uptake assays were carried out in A. fumigatus under iron-replete as well as iron-depleted conditions and distribution coefficient was determined. Based on these assays, three compounds, [68Ga]tripropanoyl(FSC) ([68Ga]TPFC), [68Ga]diacetylbutanoyl(FSC) ([68Ga]DABuFC), and [68Ga]trisuccinyl(FSC) ([68Ga]FSC(suc)3), with high, medium, and low in vitro uptake in fungal cultures, were selected for further evaluation. Stability and protein binding were evaluated and in vivo imaging performed in the A. fumigatus rat infection model. RESULTS: In vitro uptake studies using A. fumigatus revealed specific uptake of mono- and trisubstituted TAFC derivatives at RT. Lipophilicities as expressed by logD were 0.34 to - 3.80. The selected compounds displayed low protein binding and were stable in PBS and serum. Biodistribution and image contrast in PET/X-ray computed tomography of [68Ga]TPFC and [68Ga]DABuFC were comparable to [68Ga]TAFC, whereas no uptake in the infected region was observed with [68Ga]FSC(suc)3. CONCLUSIONS: Our studies show the possibility to modify TAFC without losing its properties and specific recognition by A. fumigatus. This opens also new ways for multimodality imaging or theranostics of fungal infection by introducing functionalities such as fluorescent dyes or antifungal moieties.
Department of Nuclear Medicine Medical University Innsbruck Innsbruck Austria
Division of Molecular Biology Biocenter Medical University Innsbruck Innsbruck Austria
Institute of Pharmacy Pharmaceutical Chemistry University of Innsbruck Innsbruck Austria
Research and Development Division Thailand Institute of Nuclear Technology Nakhon Nayok Thailand
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