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肺部感染的荧光镓标记铁载体的混合成像。

Hybrid Imaging of Pulmonary Infection with Fluorescent, Ga-Labelled Siderophores.

机构信息

Department of Nuclear Medicine, Medical University Innsbruck, A-6020 Innsbruck, Austria.

Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, 772-00 Olomouc, Czech Republic.

出版信息

Biomolecules. 2020 Jan 22;10(2):168. doi: 10.3390/biom10020168.

DOI:10.3390/biom10020168
PMID:31979017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7072563/
Abstract

() is a human pathogen causing severe invasive fungal infections, lacking sensitive and selective diagnostic tools. secretes the siderophore desferri-triacetylfusarinine C (TAFC) to acquire iron from the human host. TAFC can be labelled with gallium-68 to perform positron emission tomography (PET/CT) scans. Here, we aimed to chemically modify TAFC with fluorescent dyes to combine PET/CT with optical imaging for hybrid imaging applications. Starting from ferric diacetylfusarinine C ([Fe]DAFC), different fluorescent dyes were conjugated (Cy5, SulfoCy5, SulfoCy7, IRDye 800CW, ATTO700) and labelled with gallium-68 for in vitro and in vivo characterisation. Uptake assays, growth assays and live-cell imaging as well as biodistribution, PET/CT and ex vivo optical imaging in an infection model was performed. Novel fluorophore conjugates were recognized by the fungal TAFC transporter MirB and could be utilized as iron source. Fluorescence microscopy showed partial accumulation into hyphae. µPET/CT scans of an invasive pulmonary aspergillosis (IPA) rat model revealed diverse biodistribution patterns for each fluorophore. [Ga]Ga-DAFC-Cy5/SufloCy7 and -IRDye 800CW lead to a visualization of the infected region of the lung. Optical imaging of ex vivo lungs corresponded to PET images with high contrast of infection versus non-infected areas. Although fluorophores had a decisive influence on targeting and pharmacokinetics, these siderophores have potential as a hybrid imaging compounds combining PET/CT with optical imaging applications.

摘要

()是人病原体,可引起严重的侵袭性真菌感染,缺乏敏感和选择性的诊断工具。它会分泌铁载体去铁三乙酰基俘精氨酸 C(TAFC),从人体宿主中获取铁。TAFC 可以用镓-68 标记,进行正电子发射断层扫描(PET/CT)扫描。在这里,我们旨在用荧光染料化学修饰 TAFC,将 PET/CT 与光学成像相结合,用于混合成像应用。从二乙酰基俘精氨酸 C([Fe]DAFC)开始,将不同的荧光染料进行共轭(Cy5、SulfoCy5、SulfoCy7、IRDye 800CW、ATTO700)并与镓-68 标记,用于体外和体内特性分析。进行了摄取实验、生长实验和活细胞成像以及在感染模型中的生物分布、PET/CT 和离体光学成像。真菌 TAFC 转运蛋白 MirB 识别新型荧光染料缀合物,并可用作铁源。荧光显微镜显示部分荧光染料缀合物在菌丝中积累。侵袭性肺曲霉病(IPA)大鼠模型的 µPET/CT 扫描显示,每种荧光染料的生物分布模式均不同。[Ga]Ga-DAFC-Cy5/SufloCy7 和 -IRDye 800CW 可用于可视化肺部感染区域。离体肺的光学成像与感染与非感染区域具有高对比度的 PET 图像相对应。尽管荧光染料对靶向和药代动力学有决定性影响,但这些铁载体有可能成为一种将 PET/CT 与光学成像应用相结合的混合成像化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/ee020e392355/biomolecules-10-00168-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/d7bcc83017a0/biomolecules-10-00168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/c1d7a7372232/biomolecules-10-00168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/187405b9326f/biomolecules-10-00168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/346eeb60dade/biomolecules-10-00168-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/1af302b9f4e8/biomolecules-10-00168-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/022f8031f3ae/biomolecules-10-00168-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/ee020e392355/biomolecules-10-00168-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/d7bcc83017a0/biomolecules-10-00168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/c1d7a7372232/biomolecules-10-00168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/187405b9326f/biomolecules-10-00168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/346eeb60dade/biomolecules-10-00168-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/1af302b9f4e8/biomolecules-10-00168-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/022f8031f3ae/biomolecules-10-00168-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d304/7072563/ee020e392355/biomolecules-10-00168-g007.jpg

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