Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
ACS Nano. 2012 Mar 27;6(3):2361-70. doi: 10.1021/nn204625e. Epub 2012 Feb 16.
Herein we demonstrate that nanographene can be specifically directed to the tumor neovasculature in vivo through targeting of CD105 (i.e., endoglin), a vascular marker for tumor angiogenesis. The covalently functionalized nanographene oxide (GO) exhibited excellent stability and target specificity. Pharmacokinetics and tumor targeting efficacy of the GO conjugates were investigated with serial noninvasive positron emission tomography imaging and biodistribution studies, which were validated by in vitro, in vivo, and ex vivo experiments. The incorporation of an active targeting ligand (TRC105, a monoclonal antibody that binds to CD105) led to significantly improved tumor uptake of functionalized GO, which was specific for the neovasculature with little extravasation, warranting future investigation of these GO conjugates for cancer-targeted drug delivery and/or photothermal therapy to enhance therapeutic efficacy. Since poor extravasation is a major hurdle for nanomaterial-based tumor targeting in vivo, this study also establishes CD105 as a promising vascular target for future cancer nanomedicine.
在此,我们证明了通过靶向 CD105(即内皮糖蛋白),纳米石墨烯可以在体内特异性地靶向肿瘤新生血管。经过共价功能化的氧化石墨烯(GO)表现出了极好的稳定性和靶向特异性。通过连续的非侵入性正电子发射断层扫描成像和生物分布研究,对 GO 缀合物的药代动力学和肿瘤靶向效果进行了研究,这些研究通过体外、体内和离体实验得到了验证。通过引入一种活性靶向配体(TRC105,一种与 CD105 结合的单克隆抗体),功能化 GO 的肿瘤摄取得到了显著提高,这对新生血管具有特异性,几乎没有外渗,这为这些 GO 缀合物在癌症靶向药物输送和/或光热治疗方面的应用提供了依据,以增强治疗效果。由于外渗不良是纳米材料在体内进行肿瘤靶向的一个主要障碍,因此这项研究也将 CD105 确立为未来癌症纳米医学的一个有前途的血管靶向目标。