阿霉素
顺铂
多重耐药
核酸
药物输送
癌症研究
抗药性
流出
毒品携带者
药品
癌症
化学
癌细胞
药理学
化疗
纳米技术
医学
材料科学
生物
生物化学
内科学
微生物学
作者
Lingmin Zhang,Xinglong Yang,Ying Li,Wenfu Zheng,Xingyu Jiang
出处
期刊:Carbon
[Elsevier]
日期:2017-05-24
卷期号:121: 79-89
被引量:31
标识
DOI:10.1016/j.carbon.2017.05.084
摘要
The synergistic treatment with therapeutic nucleic acids and chemotherapeutics is considered to be a feasible strategy to overcome drug-resistant cancers. Herein, we constructed a novel amine dotted hollow carbon nanospheres (HCNs) to serve as a versatile platform for co-delivery of siRNA targeting multidrug resistance gene (MDR1) mRNA (siMDR1) and chemotherapeutics (Doxorubicin or Cisplatin) to fight drug-resistant cancers. The HCNs show enhanced loading capability of both siRNA and chemotherapeutics. The nanostructure down-regulates more than ∼96% of MDR1 protein expression of DOX-resistant breast cancer (MCF-7/ADR cells) and leads to ∼90% reduction of weight of MCF-7/ADR tumour on mice. Thus, the HCNs can be used as a good platform for drug delivery in cancer therapy.
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