Hyaluronic acid and Arg-Gly-Asp peptide modified Graphene oxide with dual receptor-targeting function for cancer therapy

作者：Guo, Yufeng; Xu, Haixing^*; Li, Yiping; Wu, Fengzheng; Li, Yixuan; Bao, Yun; Yan, Xiumei; Huang, Zhijun; Xu, Peihu

来源：Journal of Biomaterials Applications, 2017, 32(1): 54-65.

DOI：10.1177/0885328217712110

• Graphene oxide
• hyaluronic acid
• RGD peptide
• dual-receptor
• synergic effect
• targeting drug delivery system
• cancer therapeutic

Graphene oxide (GO) modified with hyaluronic acid (HA) and Arg-gly-asp peptide (RGD) was designed as a dual-receptor targeting drug delivery system to enhance the specificity and efficiency of anticancer drug delivery. Firstly, GO-HA-RGD conjugate was characterized to reveal its structure and morphology. Whereafter, doxorubicin (Dox) as a model drug was loaded on GO-HA-RGD carrier, which displayed a high loading rate (72.9%, GO:Dox (w/w)=1:1), pH-response and sustained drug release behavior. Cytotoxicity experiments showed that GO-HA-RGD possessed excellent biocompatibility towards SKOV-3 and HOSEpiC cells. Additionally, the GO-HA-RGD/Dox had a stronger cytotoxicity for SKOV-3 cells than either GO-HA/Dox (single receptor) or GO/Dox (no receptor). Moreover, celluar uptake studies illustrated that GO-HA-RGD conjugate could be effectively taken up by SKOV-3 cells via a synergic effect of CD44-HA and integrin-RGD mediated endocytosis. Hence, GO-HA-RGD nanocarrier is able to be a promising platform for targeted cancer therapeutic.

• 出版日期2017-7
• 单位武汉理工大学