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A graphene quantum dot@Fe3O4@SiO2 based nanoprobe for drug delivery sensing and dual-modal fluorescence and MRI imaging in cancer cells

机译:基于石墨烯量子点@ Fe3O4 @ SiO2的纳米探针,用于癌细胞中的药物传递传感以及双峰荧光和MRI成像

摘要

A novel graphene quantum dot (GQD)@Fe3O4@SiO2 based nanoprobe was reported for targeted drug delivery, sensing, dual-modal imaging and therapy. Carboxyl-terminated GQD (C-GQD) was firstly conjugated with Fe3O4@SiO2 and then functionalized with cancer targeting molecule folic acid (FA). DOX drug molecules were then loaded on GQD surface of Fe3O4@SiO2@GQD-FA nanoprobe via pi-pi stacking, which resulted in Fe3O4@SiO2@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 Fe3O4@SiO2@GQD-FA/DOX nanoprobe. Cell viability study demonstrated the low cytotoxicity of Fe3O4@SiO2@GQD-FA nanocarrier and the enhanced therapeutic efficacy of Fe3O4@SiO2@GQD-FA/DOX nanoprobe for cancer cells. This luminomagnetic nanoprobe will be a potential platform for cancer accurate diagnosis and therapy.
机译:据报道,一种新颖的石墨烯量子点(GQD)@ Fe3O4 @ SiO2基纳米探针可用于靶向药物递送,传感,双峰成像和治疗。首先将羧基封端的GQD(C-GQD)与Fe3O4 @ SiO2偶联,然后用靶向癌症的分子叶酸(FA)进行功能化。然后通过pi-pi堆叠将DOX药物分子装载到Fe3O4 @ SiO2 @ GQD-FA纳米探针的GQD表面上,从而产生了基于FRET机理的Fe3O4 @ SiO2 @ GQD-FA / DOX共轭物,其中GQD作为供体分子,DOX作为受体分子。同时,我们使用这种Fe3O4 @ SiO2 @ GQD-FA / DOX纳米探针成功地对活Hela细胞进行了体外MRI和荧光成像,并监测了细胞内药物释放过程。细胞活力研究表明,Fe3O4 @ SiO2 @ GQD-FA纳米载体的细胞毒性低,并且Fe3O4 @ SiO2 @ GQD-FA / DOX纳米探针对癌细胞的治疗作用增强。这种光磁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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