Near-infrared nanoparticles based on indocyanine green-conjugated albumin: a versatile platform for imaging-guided synergistic tumor chemo-phototherapy with temperature-responsive drug releas

被引:11
|
作者
Ma, Yuxin [1 ]
Liu, Xiaohua [1 ]
Ma, Qianli [2 ]
Liu, Yizhi [3 ]
机构
[1] Jinan Stomatol Hosp, Jinan 250001, Shandong, Peoples R China
[2] Shandong Univ, Sch & Hosp Stomatol, Jinan 250001, Shandong, Peoples R China
[3] Binzhou Med Sch, Binzhou 256603, Shandong, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
关键词
artemisinin; indocyanine green; theranostic; imaging-guided tumor therapy; chemo-phototherapy; PHOTODYNAMIC THERAPY; LIPID NANOPARTICLES; GRAPHENE OXIDE; CANCER; ANTITUMOR; DELIVERY; CHEMOTHERAPY; COMBINATION; ARTEMISININ; NANOPLATFORM;
D O I
10.2147/OTT.S183887
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The aim of this study was to develop a multifunctional theranostic agent based on BSA nanoparticles (NPs), which loaded artemisinin (ART) and co-conjugated with indocyanine green (ICG) and arginine-glycine-aspartic acid (RGD) peptide (RGD-indocyanine green-Bovine Serum Albumin- artemisinin [IBA] NPs). Materials and methods: The physicochemical parameters of RGD-IBA NPs were characterized in terms of the particle size, zeta potential, morphology, entrapment efficiency, drug loading, in vitro release behavior, photothermal and photodynamic effect, and in vitro anticancer ability. In vivo fluorescence and thermal imaging as well as antitumor studies were also evaluated. Results: The tumor chemotherapeutic effects of ART and the ability of fluorescence imaging, hyperthermia generation and reactive oxygen species production of ICG and tumor-targeting RGD were integrated to achieve RGD-IBA NPs for imaging-guided tumor-targeted chemotherapy/ photothermal/photodynamic therapy (chemo-phototherapy). The RGD-IBANPs showed enhanced physiological stability and photo-stability compared. with free ART and ICG. In addition, they were temperature-responsive; their sizes increased with increasing temperature between 25 degrees C and 55 degrees C, thereby leading to drug release upon the irradiation with near infrared (NIR) laser. In vivo fluorescence images of tumor-bearing mice showed that the RGD-IBA NPs could highly and passively reach the targeted tumor region with maximum accumulation at 24 hours post-intravenous injection. The in vitro and in vivo results demonstrated that the RGD-IBA NPs not only have good biocompatibility, but also are highly efficient tumor synergistic ehemo-pholotherapeutie agents. Condusion: Through this study, it was found that RGD-IBAA NPs could potentially be a very promising tumor theranostic agent.
引用
收藏
页码:8517 / 8528
页数:12
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