HSA/PSS Coated Gold Nanorods as Thermo-Triggered Drug Delivery Vehicles for Combined Cancer Photothermal Therapy and Chemotherapy

被引:4
作者
Tu, Ting-Yu [1 ,2 ]
Yang, Shu-Jyuan [1 ,2 ,3 ,4 ]
Wang, Chung-Hao [3 ,4 ]
Lee, Shin-Yu [1 ,2 ]
Shieh, Ming-Jium [1 ,2 ,5 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Biomed Engn, 1,Sect 1,Jen Ai Rd, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Engn, 1,Sect 1,Jen Ai Rd, Taipei 100, Taiwan
[3] Genee Tech Co Ltd 2F, 661 Bannan Rd, New Taipei 235, Taiwan
[4] Apius Bio Inc 1F, 92 Daxin St, New Taipei 234, Taiwan
[5] Natl Taiwan Univ Hosp & Coll Med, Dept Oncol, 7 Chung Shan South Rd, Taipei 100, Taiwan
来源
OPTICAL METHODS FOR TUMOR TREATMENT AND DETECTION: MECHANISMS AND TECHNIQUES IN PHOTODYNAMIC THERAPY XXVII | 2018年 / 10476卷
关键词
gold nanorod; human serum albumin; chemotherapy; photothermal therapy; control drug release; IRON-OXIDE NANOPARTICLES; OVERCOME MULTIDRUG-RESISTANCE; MRI CONTRAST; STEM-CELLS; FOLIC-ACID; ALBUMIN; RELEASE; DOXORUBICIN; MECHANISMS; MICELLES;
D O I
10.1117/12.2289273
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Drug delivery systems combined multimodal therapy strategies are very promising in cancer theranostic applications. In this work, a new drug-delivery vehicles based on human serum albumin (HSA)-coated gold nanorods (GNR/PSS/HSA NPs) was developed. The success of coating was verified by transmission electron microscopy (TEM), zeta potential and fourier transform infrared spectroscopy (FTIR). Furthermore, it is demonstrated that doxorubicin (DOX) is successfully loaded among multilayered gold nanorods by the electrostatic and hydrophobic force, and DOX@GNR/PSS/HSA NPs were highly biocompatible and stable in various physiological solutions. The NPs possess strong absorbance in near-infrared (NIR) region, and high photothermal conversion efficiency for outstanding photothermal therapy applications. A bimodal drug release triggered by proteinase or NIR irradiation has been revealed, resulting in a significant chemotherapeutic effect in tumor sites because of the preferential drug accumulation and triggered release. Importantly, the in vitro and in vivo experiments demonstrated that DOX@GNR/PSS/HSA NPs, which combined photothermal and chemotherapy for cancer therapy, revealing a remarkably superior synergistic anticancer effect over either monotherapy. All these results suggested a considerable potential of DOX@GNR/PSS/HSA NPs nano-platform for antitumor therapy.
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页数:18
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