Hierarchical nanocomposites of graphene oxide and PEGylated protoporphyrin as carriers to load doxorubicin hydrochloride for trimodal synergistic therapy

被引:39
作者
Su, Ting [1 ]
Cheng, Furong [1 ]
Yan, Jianqin [1 ]
Cao, Jun [1 ]
Luo, Kui [2 ]
Pu, Yuji [1 ]
He, Bin [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Radiol, HMRRC, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
PROLONGED CIRCULATION TIME; POLYMERIC NANOPARTICLES; CONTROLLED-RELEASE; DELIVERY; PLATFORM; MICELLES; CHEMOTHERAPEUTICS; NANOTECHNOLOGY; NANOMATERIALS; NANOCARRIER;
D O I
10.1039/c8tb00733k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Multimodal and synergistic therapy of cancer has appeared as one of the most promising strategies in treating cancer. Here, we report a supramolecular hierarchical nanocomposite for combination photodynamic, photothermal, and chemotherapy. Graphene oxide (GO, photothermal agent for photothermal therapy, PTT), protoporphyrin IX (PpIX, photosensitizer for photodynamic therapy, PDT), and hydrophilic anticancer drug doxorubicin hydrochloride (DOX<bold>HCl</bold>, therapeutic for chemotherapy) are involved in hierarchical self-assembled nanocomposites via supramolecular interactions. PEGylated PpIX (PEG-PpIX) is prepared to improve the stability of GO in physiological conditions. The nanocomposite GO(PEG-PpIX) is non-cytotoxic in the dark and phototoxic with light irradiation to exhibit efficient PTT and PDT effects. The drug loading content of the nanocomposite DOX/GO(PEG-PpIX) is as high as 15.9% and the drug release shows a pH-dependent profile. The combined PDT, PTT, and chemotherapy shows an excellent in vivo antitumor effect and side effect reduction. This work presents a facile yet robust strategy to fabricate a nanocomposite for multimodal synergistic therapy.
引用
收藏
页码:4687 / 4696
页数:10
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