利用还原氧化石墨烯对活体小鼠的肿瘤血管进行靶向和成像。

Tumor vasculature targeting and imaging in living mice with reduced graphene oxide.

机构信息

Materials Science Program, University of Wisconsin-Madison, Madison, WI 53705-2275, USA.

出版信息

Biomaterials. 2013 Apr;34(12):3002-9. doi: 10.1016/j.biomaterials.2013.01.047. Epub 2013 Jan 29.

Abstract

Graphene-based nanomaterials have attracted tremendous attention in the field of biomedicine due to their intriguing properties. Herein, we report tumor vasculature targeting and imaging in living mice using reduced graphene oxide (RGO), which was conjugated to the anti-CD105 antibody TRC105. The RGO conjugate, (64)Cu-NOTA-RGO-TRC105, exhibited excellent stability in vitro and in vivo. Serial positron emission tomography (PET) imaging studies non-invasively assessed the pharmacokinetics and demonstrated specific targeting of (64)Cu-NOTA-RGO-TRC105 to 4T1 murine breast tumors in vivo, compared to non-targeted RGO conjugate ((64)Cu-NOTA-RGO). In vivo (e.g., blocking 4T1 tumor uptake with excess TRC105), in vitro (e.g., flow cytometry), and ex vivo (e.g., histology) experiments confirmed the specificity of (64)Cu-NOTA-RGO-TRC105 for tumor vascular CD105. Since RGO exhibits desirable properties for photothermal therapy, the tumor-specific RGO conjugate developed in this work may serve as a promising theranostic agent that integrates imaging and therapeutic components.

摘要

基于石墨烯的纳米材料因其独特的性质在生物医药领域引起了极大的关注。在这里,我们报告了使用还原氧化石墨烯(RGO)与抗 CD105 抗体 TRC105 缀合的方法,在活小鼠中实现肿瘤血管靶向和成像。RGO 缀合物(64)Cu-NOTA-RGO-TRC105 在体外和体内均表现出优异的稳定性。连续正电子发射断层扫描(PET)成像研究非侵入性地评估了药代动力学,并证明了(64)Cu-NOTA-RGO-TRC105 与 4T1 小鼠乳腺癌的特异性靶向,与非靶向 RGO 缀合物(64)Cu-NOTA-RGO 相比。体内(例如,用过量的 TRC105 阻断 4T1 肿瘤摄取)、体外(例如,流式细胞术)和离体(例如,组织学)实验证实了(64)Cu-NOTA-RGO-TRC105 对肿瘤血管 CD105 的特异性。由于 RGO 表现出用于光热治疗的理想性质,因此本工作中开发的肿瘤特异性 RGO 缀合物可用作一种有前途的治疗诊断一体化试剂,将成像和治疗成分整合在一起。

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