介孔二氧化硅
体内
细胞毒性
纳米技术
胶体金
上皮细胞粘附分子
体外
粘附
材料科学
细胞粘附
纳米颗粒
PEG比率
化学
生物物理学
细胞
介孔材料
生物化学
有机化学
生物
财务
催化作用
经济
生物技术
作者
Maryam Babaei,Khalil Abnous,Seyed Mohammad Taghdisi,Sara Amel Farzad,Mohammad Taghi Peivandi,Mohammad Ramezani,Mona Alibolandi
出处
期刊:Nanomedicine
[Future Medicine]
日期:2017-05-18
卷期号:12 (11): 1261-1279
被引量:69
标识
DOI:10.2217/nnm-2017-0028
摘要
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.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.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.This work introduces a novel strategy for developing multimodal NPs via nanoparticulate hybrid materials.
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