Targeting Chemophotothermal Therapy of Hepatoma by Gold Nanorods/Graphene Oxide Core/Shell Nanocomposites

被引:117
作者
Xu, Cheng
Yang, Darong
Mei, Lin
Li, Qinhong [1 ]
Zhu, Haizhen
Wang, Taihong
机构
[1] Hunan Univ, Key Lab Micronano Optoelect Devices, Minist Educ, Changsha 410082, Hunan, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
graphene oxide; gold nanorods; core/shell materials; drug delivery; photothermal therapy; cancer therapy; CHEMO-PHOTOTHERMAL THERAPY; PEGYLATED GRAPHENE OXIDE; SPHERICAL NUCLEIC-ACIDS; CONJUGATED GRAPHENE; DRUG-DELIVERY; NANO-GRAPHENE; IN-SITU; NANOPARTICLES; MICE; DERIVATIVES;
D O I
10.1021/am404714w
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanographene oxide (NGO) are highly suitable to be the shells of inorganic nanomaterials to enhance their biocompatibility and hydrophilicity for biomedical applications while retaining their useful photonic, magnetic, or radiological functions. In this study, a novel nanostructure with gold nanorods (AuNRs) encapsulated in NGO shells is developed to be an ultraefficient chemophotothermal cancer therapy agent. The NGO shells decrease the toxicity of surfactant-coated AuNRs and provide anchor points for the conjugation of hyaluronic acid (HA). The HA-conjugated NGO-enwrapped AuNR nanocomposites (NGOHA-AuNRs) perform higher photothernial efficiency than AuNRs and have the capability of targeting hepatoma Huh-7 cells. NGOHA-AuNR is applied to load doxorubicin (DOX), and it exhibits pH-responsive and near-infrared light-triggered drug-release properties. Chemophotothermal combined therapy by NGOIA-AuNRs-DOX performs 1.5-fold and 4-fold higher targeting cell death rates than single chemotherapy and photothermal therapy, respectively, with biosafety to nontargeting cells simultaneously. Furthermore, our strategy could be extended to constructing other NGO-encapsulated functional nanomaterial-based carrier systems.
引用
收藏
页码:12911 / 12920
页数:10
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