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用于细胞尺度双模态成像的靶向分子成像剂。

Targeted molecular imaging agents for cellular-scale bimodal imaging.

作者信息

Manning H Charles, Goebel Timothy, Thompson Reid C, Price Ronald R, Lee Haakil, Bornhop Darryl J

机构信息

Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37232, USA.

出版信息

Bioconjug Chem. 2004 Nov-Dec;15(6):1488-95. doi: 10.1021/bc049904q.

Abstract

Molecular imaging is a powerful tool that has the ability to elucidate biochemical mechanisms and signal the early onset of disease. Overexpression of the peripheral benzodiazepine receptor (PBR) has been observed in a variety disease states, including glioblastoma, breast cancer, and Alzheimer's disease. Thus, the PBR could be an attractive target for molecular imaging. In this paper, the authors report cellular uptake and multimodal (MRI and fluorescence) imaging of PBR-overexpressing C6 glioblastoma (brain cancer) cells using a cocktail administration approach and a new PBR targeted lanthanide chelate molecular imaging agent.

摘要

分子成像是一种强大的工具,能够阐明生化机制并提示疾病的早期发作。在外周苯二氮䓬受体(PBR)的过表达已在多种疾病状态中被观察到,包括胶质母细胞瘤、乳腺癌和阿尔茨海默病。因此,PBR可能是分子成像的一个有吸引力的靶点。在本文中,作者报告了使用联合给药方法和一种新的靶向PBR的镧系螯合物分子成像剂对过表达PBR的C6胶质母细胞瘤(脑癌)细胞进行细胞摄取和多模态(MRI和荧光)成像。

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