کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5431843 | 1508826 | 2017 | 11 صفحه PDF | دانلود رایگان |

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.
We construct a novel amine-coated hollow carbon nanospheres (HCNs), which serve as a versatile platform for co-delivery of siRNA and chemotherapeutics (DOX or Cis) to fight drug-resistant cancers. The nanostructures exhibit enhanced nucleic acid and chemotherapeutics delivery, effective gene regulation, and synergistically inhibit drug-resistant cancers in vitro and in vivo.Figure optionsDownload high-quality image (326 K)Download as PowerPoint slide
Journal: Carbon - Volume 121, September 2017, Pages 79–89