Integrin αvβ3-targeted polydopamine-coated gold nanostars for photothermal ablation therapy of hepatocellular carcinoma

被引:25
|
作者
Li, Yang [1 ]
Hu, Ping [1 ]
Wang, Xiali [2 ]
Hou, Xu [3 ]
Liu, Fengzhen [4 ]
Jiang, Xiaohong [1 ,5 ]
机构
[1] Liaocheng Peoples Hosp, Zhong Yuan Acad Biol Med, 67 Dongchang West Rd, Liaocheng 252000, Shandong, Peoples R China
[2] Liaocheng Peoples Hosp, Clin Lab, 67 Dongchang West Rd, Liaocheng 252000, Shandong, Peoples R China
[3] Liaocheng Peoples Hosp, Dept Hepatobiliary Surg, 67 Dongchang West Rd, Liaocheng 252000, Shandong, Peoples R China
[4] Liaocheng Univ, Liaocheng Peoples Hosp, Med Coll, 67 Dongchang West Rd, Liaocheng 252000, Shandong, Peoples R China
[5] Shandong Univ, Sch Basic Med Sci, 44 Wenhua West Rd, Jinan 250012, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
polydopamine-coated gold nanostars; RGD peptide; targeted photothermal therapy; hepatocellular carcinoma; LYSOSOMAL MEMBRANE PERMEABILIZATION; PHOTODYNAMIC THERAPY; ANTICANCER ACTIVITY; NANORODS; NANOPARTICLES; SPECTROSCOPY; COMPLEXES; APOPTOSIS; RELEASE; RAMAN;
D O I
10.1093/rb/rbab046
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
Photothermal therapy (PTT) has emerged as a promising cancer therapeutic method. In this study, Arg-Gly-Asp (RGD) peptide-conjugated polydopamine-coated gold nanostars (Au@PDA-RGD NPs) were prepared for targeting PTT of hepatocellular carcinoma (HCC). A polydopamine (PDA) shell was coated on the surface of gold nanostars by the oxidative self-polymerization of dopamine (termed as Au@PDA NPs). Au@PDA NPs were further functionalized with polyethylene glycol and RGD peptide to improve biocompatibility as well as selectivity toward the HCC cells. Au@PDARGD NPs showed an intense absorption at 822 nm, which makes them suitable for near-infraredexcited PTT. Our results indicated that the Au@PDA-RGD NPs were effective for the PTT therapy of the aVb3 integrin receptor-overexpressed HepG2 cells in vitro. Further antitumor mechanism studies showed that the Au@PDA-RGD NPs-based PTT induced human liver cancer cells death via the mitochondrial-lysosomal and autophagy pathways. In vivo experiments showed that Au@PDARGD NPs had excellent tumor treatment efficiency and negligible side effects. Thus, our study showed that Au@PDA-RGD NPs could offer an excellent nanoplatform for PTT of HCC.
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页数:14
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