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基于透明质酸-神经酰胺的光学/MR 双模式成像纳米探针用于癌症诊断。

Hyaluronic acid-ceramide-based optical/MR dual imaging nanoprobe for cancer diagnosis.

机构信息

College of Pharmacy, Sunchon National University, Sunchon 540-950, Republic of Korea.

出版信息

J Control Release. 2012 Aug 20;162(1):111-8. doi: 10.1016/j.jconrel.2012.06.011. Epub 2012 Jun 15.

DOI:10.1016/j.jconrel.2012.06.011
PMID:22709587
Abstract

Hyaluronic acid-ceramide (HACE)-based nanoprobes for magnetic resonance (MR) and optical imaging were developed for cancer diagnosis. Diethylenetriaminepentaacetic dianhydride (DTPA) was conjugated to HACE for the chelation of gadolinium (Gd) as an MR contrast agent. Cy5.5 was also conjugated to the HACE backbone as a near-infrared fluorescence (NIRF) imaging dye. The self-assembled HACE-based nanoprobe, Cy5.5-HACE-DTPA-Gd, exhibited a uniformly distributed particle size and morphological shape. The HACE-based nanoprobe did not induce serious cytotoxicity in U87-MG (low expression of CD44 receptor) and SCC7 (high expression of CD44 receptor) cells. The cellular uptake efficiency of the HACE-based nanoprobe was higher in SCC7 cells than in U87-MG cells, indicating an HA-CD44 receptor interaction. In vitro MR signal enhancement of the HACE-based nanoprobe was confirmed compared with a commercial formulation (Magnevist). Moreover, in vivo MR contrast enhancement of the HACE-based nanoprobe in the tumor region was verified in an SCC7 tumor xenograft mouse model. The tumor targetability of the developed nanoprobe was monitored by an NIRF imaging study, and improved accumulation of the nanoprobe in the tumor region was observed. Therefore, this HACE-based dual-imaging nanoprobe can be used to make a more accurate diagnosis of cancer based on its passive and active tumor targeting strategies.

摘要

基于透明质酸-神经酰胺(HACE)的纳米探针被开发用于磁共振(MR)和光学成像,用于癌症诊断。二亚乙基三胺五乙酸二酐(DTPA)与 HACE 缀合,以螯合钆(Gd)作为磁共振对比剂。Cy5.5 也与 HACE 主链缀合,作为近红外荧光(NIRF)成像染料。自组装的基于 HACE 的纳米探针 Cy5.5-HACE-DTPA-Gd 表现出均匀分布的粒径和形态。基于 HACE 的纳米探针在 U87-MG(低表达 CD44 受体)和 SCC7(高表达 CD44 受体)细胞中没有引起严重的细胞毒性。基于 HACE 的纳米探针在 SCC7 细胞中的细胞摄取效率高于 U87-MG 细胞,表明存在 HA-CD44 受体相互作用。与商业制剂(Magnevist)相比,证实了基于 HACE 的纳米探针的体外 MR 信号增强。此外,在 SCC7 肿瘤异种移植小鼠模型中验证了基于 HACE 的纳米探针在肿瘤区域的体内 MR 对比增强。通过 NIRF 成像研究监测了开发的纳米探针的肿瘤靶向性,并观察到纳米探针在肿瘤区域的积累增加。因此,这种基于 HACE 的双模式成像纳米探针可以基于其被动和主动肿瘤靶向策略,更准确地诊断癌症。

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