细胞毒性
体内
阿霉素
Zeta电位
化学
小干扰RNA
膀胱癌
纳米材料
癌症研究
药理学
材料科学
生物物理学
核化学
纳米技术
医学
癌症
体外
生物化学
化疗
生物
转染
纳米颗粒
外科
内科学
生物技术
基因
作者
Wagner José Fávaro,J. C. Souza,Luiz Alberto Bandeira Ferreira,Marcelo Bispo de Jesus,Nélson Durán,Petra Karla Böckelmann,Juliana S. Bernardes,Nelsón Durán
出处
期刊:Advances in Natural Sciences: Nanoscience and Nanotechnology
[IOP Publishing]
日期:2020-05-27
卷期号:11 (2): 025016-025016
被引量:1
标识
DOI:10.1088/2043-6254/ab9194
摘要
Two types of graphene oxide (GO) hybrids were synthesised for the administration of doxorubicin (DOX, named GO-CO-DOX) and interfering RNA - siRNA (named GO-PEG-PEI/siRNA). These nanomaterials were used for intervention on vascular endothelial growth factor (VEGF) that represents an important strategy to block the formation of new vessels to inhibit cancer progression. For the delivery of DOX, it was incorporated into GO, while for the delivery of siRNA, GO was covalently bonded with the cationic polyethyleneimine (PEI) and then complexed with siRNA. The nanostructures were characterised by attenuated total reflection ATR-FTIR, zeta potential, x-ray photoelectron spectroscopy (XPS), x-ray diffraction (XRD), and transmission electron microscopy (TEM). The cytotoxicity studies with GO-PEG-PEI and GO-PEG-PEI/siRNA systems showed that both formulations have IC50 values of around 100 μg ml−1. The systems were administered in vivo to investigate their antitumor effects against non-muscle-invasive bladder cancer (NMIBC) and showed to be promising for the treatment of NMIBC.
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