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基于石墨烯量子点@FeO@SiO 的纳米探针用于药物输送传感及癌细胞的双模式荧光和 MRI 成像。

A graphene quantum dot@FeO@SiO based nanoprobe for drug delivery sensing and dual-modal fluorescence and MRI imaging in cancer cells.

机构信息

Interdisciplinary Division of Biomedical Engineering, the Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, PR China.

Department of Applied Physics, the Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, PR China.

出版信息

Biosens Bioelectron. 2017 Jun 15;92:489-495. doi: 10.1016/j.bios.2016.10.076. Epub 2016 Oct 28.

Abstract

A novel graphene quantum dot (GQD)@FeO@SiO based nanoprobe was reported for targeted drug delivery, sensing, dual-modal imaging and therapy. Carboxyl-terminated GQD (C-GQD) was firstly conjugated with FeO@SiO and then functionalized with cancer targeting molecule folic acid (FA). DOX drug molecules were then loaded on GQD surface of FeO@SiO@GQD-FA nanoprobe via pi-pi stacking, which resulted in FeO@SiO@GQD-FA/DOX conjugates based on a FRET mechanism with GQD as donor molecules and DOX as acceptor molecules. Meanwhile, we successfully performed in vitro MRI and fluorescence imaging of living Hela cells and monitored intracellular drug release process using this FeO@SiO@GQD-FA/DOX nanoprobe. Cell viability study demonstrated the low cytotoxicity of FeO@SiO@GQD-FA nanocarrier and the enhanced therapeutic efficacy of FeO@SiO@GQD-FA/DOX nanoprobe for cancer cells. This luminomagnetic nanoprobe will be a potential platform for cancer accurate diagnosis and therapy.

摘要

一种新型的基于石墨烯量子点(GQD)@FeO@SiO 的纳米探针被报道用于靶向药物输送、传感、双模式成像和治疗。首先将羧基化的 GQD(C-GQD)与 FeO@SiO 偶联,然后用癌症靶向分子叶酸(FA)进行功能化。DOX 药物分子通过 π-π 堆积加载到 FeO@SiO@GQD-FA 纳米探针的 GQD 表面上,形成基于 FRET 机制的 FeO@SiO@GQD-FA/DOX 缀合物,其中 GQD 作为供体分子,DOX 作为受体分子。同时,我们成功地对活的 Hela 细胞进行了体外 MRI 和荧光成像,并使用这种 FeO@SiO@GQD-FA/DOX 纳米探针监测了细胞内药物释放过程。细胞活力研究表明,FeO@SiO@GQD-FA 纳米载体的细胞毒性低,FeO@SiO@GQD-FA/DOX 纳米探针对癌细胞的治疗效果增强。这种发光磁性纳米探针将成为癌症精确诊断和治疗的潜在平台。

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