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Hyaluronic Acid-Encapsulated Platinum Nanoparticles for Targeted Photothermal Therapy of Breast Cancer
被引:35
|作者:
Zhu, Yuyang
[1
]
Li, Wei
[2
]
Zhao, Xin
[1
]
Zhou, Zhengjie
[1
]
Wang, Yitong
[1
]
Cheng, Yiyun
[1
]
Huang, Quan
[3
]
Zhang, Qiang
[1
]
机构:
[1] East China Normal Univ, Sch Life Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China
[2] Second Mil Med Univ, Changzheng Hosp, Dept Stomatol, Shanghai 200003, Peoples R China
[3] Second Mil Med Univ, Changzheng Hosp, Dept Orthoped Oncol, Shanghai 200003, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Photothermal Therapy;
Hyaluronic Acid;
Platinum Nanoparticles;
Tumor Targeting;
Breast Cancer;
IN-VIVO;
PHOTODYNAMIC THERAPY;
SILICA NANOPARTICLES;
RECEPTOR LYVE-1;
DRUG-DELIVERY;
LUNG-CANCER;
CELLS;
DOXORUBICIN;
CARCINOMA;
CD44;
D O I:
10.1166/jbn.2017.2446
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Targeted photothermal therapy (PTT) can improve the therapeutic outcomes and reduce side effects in cancer treatment. However, additional functionality means additional synthetic steps, increased risk of toxicity and complex behavior and effects in vivo. Herein, we developed a one-pot method to prepare tumor-targeted photothermal nanoparticles. Hyaluronic acid (HA), an anionic glycosaminoglycan that targets tumors via overexpressed cluster determinant 44 (CD44), was used as a polymer stabilizer to synthesize HA-encapsulated platinum nanoparticles (HA/Pt). The in vitro experiments demonstrated that HA/Pt were more efficiently internalized by cancer cells overexpressing CD44 compared with the nontumor targeting alginate acid-encapsulated Pt nanoparticles (AA/Pt). The in vivo studies revealed that HA/Pt accumulated more in CD44-overexpressing tumor than AA/Pt, and more efficiently inhibited tumor growth via PTT. Our study developed an innovative method for facile fabrication of tumor-targeting photothermal nanoparticles.
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页码:1457 / 1467
页数:11
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