The Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Angew Chem Int Ed Engl. 2019 Jul 15;58(29):9871-9875. doi: 10.1002/anie.201904722. Epub 2019 Jun 24.
While carbon dots (C-dots) have been extensively investigated pertaining to their fluorescent, phosphorescent, electrochemiluminescent, optoelectronic, and catalytic features, their inherent chemical exchange saturation transfer magnetic resonance imaging (CEST MRI) properties are unknown. By virtue of their hydrophilicity and abundant exchangeable protons of hydroxyl, amine, and amide anchored on the surface, we report here that C-dots can be adapted as effective diamagnetic CEST (diaCEST) MRI contrast agents. As a proof-of-concept demonstration, human glioma cells were labeled with liposomes with or without encapsulated C-dots and implanted in mouse brain. In vivo CEST MRI was able to clearly differentiate labeled cells from non-labeled cells. The present findings may encourage new applications of C-dots for in vivo imaging in deep tissues, which is currently not possible using conventional fluorescent (near-infrared) C-dots.
虽然碳点 (C-dots) 因其荧光、磷光、电化学发光、光电和催化特性而得到了广泛的研究,但它们固有的化学交换饱和转移磁共振成像 (CEST MRI) 特性尚不清楚。由于其亲水性以及表面上附着的羟基、胺和酰胺的丰富可交换质子,我们在此报告 C-dots 可以被用作有效的抗磁性 CEST(diaCEST)MRI 对比剂。作为概念验证演示,用人神经胶质瘤细胞用或不用封装的 C-dots 的脂质体进行标记,并植入小鼠脑内。体内 CEST MRI 能够清楚地区分标记细胞与非标记细胞。目前的发现可能会鼓励将 C-dots 用于深层组织的体内成像的新应用,而这目前使用传统的荧光(近红外)C-dots 是不可能的。