Functionalized boron nanosheets as an intelligent nanoplatform for synergistic low-temperature photothermal therapy and chemotherapy

被引:67
作者
Fu, Zi [1 ]
Williams, Gareth R. [2 ]
Niu, Shiwei [1 ]
Wu, Jianrong [3 ]
Gao, Feng [4 ]
Zhang, Xuejing [1 ]
Yang, Yanbo [1 ]
Li, Yu [1 ]
Zhu, Li-Min [1 ]
机构
[1] Donghua Univ, Coll Chem Chem Engn & Biotechnol, Shanghai 201620, Peoples R China
[2] UCL, Sch Pharm, 29-39 Brunswick Sq, London WC1N 1AX, England
[3] Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6, Shanghai Inst Ultrasound Med, Shanghai 200233, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Shanghai Gen Hosp, Dept Ultrasound, Shanghai 201600, Peoples R China
关键词
CANCER; DELIVERY; CHEMISTRY; PLATFORM; CELLS;
D O I
10.1039/d0nr02291h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, an innovative boron-based multifunctional nanoplatform was developed for synergistic chemotherapy/low temperature photothermal therapy (PTT). This platform is functionalized with a cRGD peptide to allow the targeting of alpha(v)beta(3)integrin, which is over-expressed in the cells of tumors. The nanoparticles were further loaded with the chemotherapeutic drug doxorubicin (DOX) and a heat shock protein inhibitor (17AAG), and high loading capacities for both DOX (603 mg g(-1)B-PEG-cRGD) and 17AAG (417 mg g(-1)) were obtained. The resultant DOX-17AAG@B-PEG-cRGD system shows both pH-controlled and near-infrared (NIR)-induced DOX and 17AAG release. It also provides significantly enhanced cellular uptake in cancerous cells over healthy cells. The presence of 17AAG allows low-temperature PTT to be combined with chemotherapy with DOX, resulting in highly effective anti-cancer activity. This has been confirmed by bothin vitroassays and using anin vivomurine cancer model. It is expected that such a multifunctional nanoplatform can serve as a promising candidate for cancer therapy.
引用
收藏
页码:14739 / 14750
页数:12
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