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用于肝细胞癌的具有金质守门人的诊疗上皮细胞粘附分子靶向介孔二氧化硅纳米颗粒的合成

Synthesis of theranostic epithelial cell adhesion molecule targeted mesoporous silica nanoparticle with gold gatekeeper for hepatocellular carcinoma.

作者信息

Babaei Maryam, Abnous Khalil, Taghdisi Seyed Mohammad, Amel Farzad Sara, Peivandi Mohammad Taghi, Ramezani Mohammad, Alibolandi Mona

机构信息

Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran.

出版信息

Nanomedicine (Lond). 2017 Jun;12(11):1261-1279. doi: 10.2217/nnm-2017-0028. Epub 2017 May 18.

Abstract

AIM

In this study, we report the fabrication of epithelial cell adhesion molecule targeted 5-fluorouracil (5-FU) encapsulated PEGylated mesoporous silica nanoparticles (NPs) hybridized with gold NPs (PEG-Au@Si-5-FU) as gatekeeper for theranostic applications.

MATERIALS & METHODS: The prepared targeted and nontargeted formulations were evaluated in vitro in terms of their cellular internalization and toxicity. The prepared theranostic hybrid system was also implemented for computed tomography of HepG2 tumor-bearing nude mice in vivo.

RESULTS

Fluorescence microscopy and MTT assay demonstrated that the developed epithelial cell adhesion molecule-PEG-Au@Si-5-FU had higher cytotoxicity than nontargeted PEG-Au@Si-5-FU in 2D and 3D HepG2 cell cultures. Moreover, the targeted hybrid system was preferentially accumulated in HepG2 tumor cells in vitro and in vivo.

CONCLUSION

This work introduces a novel strategy for developing multimodal NPs via nanoparticulate hybrid materials.

摘要

目的

在本研究中,我们报道了制备上皮细胞粘附分子靶向的5-氟尿嘧啶(5-FU)包裹的聚乙二醇化介孔二氧化硅纳米粒子(NPs),并与金纳米粒子(PEG-Au@Si-5-FU)杂交,作为用于治疗诊断应用的守门人。

材料与方法

对制备的靶向和非靶向制剂进行体外细胞内化和毒性评估。制备的治疗诊断杂交系统也用于荷HepG2肿瘤裸鼠的体内计算机断层扫描。

结果

荧光显微镜和MTT分析表明,在二维和三维HepG2细胞培养中,所开发的上皮细胞粘附分子-PEG-Au@Si-5-FU比非靶向的PEG-Au@Si-5-FU具有更高的细胞毒性。此外,靶向杂交系统在体外和体内均优先积聚在HepG2肿瘤细胞中。

结论

这项工作介绍了一种通过纳米颗粒杂化材料开发多模态纳米粒子的新策略。

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