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A multi-bioresponsive self-assembled nano drug delivery system based on hyaluronic acid and geraniol against liver cancer
被引:19
|作者:
Duan, Shaofeng
[1
]
Xia, Yifan
[1
]
Tian, Xue
[1
]
Cui, Jie
[1
]
Zhang, Xin
[1
]
Yang, Qian
[1
]
Zhao, Tingkui
[1
]
Lin, Yuxia
[1
]
Zhang, Feng
[1
]
Zhang, Xiaoju
[2
]
Cen, Juan
[1
]
机构:
[1] Henan Univ, Sch Pharm, Key Lab Nat Med & Immune Engn, Kaifeng 475004, Peoples R China
[2] Zhengzhou Univ, Henan Prov Peoples Hosp, Dept Resp & Crit Care Med, Peoples Hosp, Zhengzhou 450003, Peoples R China
关键词:
Geraniol;
Hyaluronic acid;
Self-assembled;
Multi-bioresponsive;
Hepatocellular carcinoma;
IN-VITRO;
TUMOR;
CARCINOMA;
NANOPARTICLES;
CONJUGATE;
LIPOSOMES;
PRODRUG;
D O I:
10.1016/j.carbpol.2023.120695
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Herein, a multi-bioresponsive self-assembled nano-drug delivery system (HSSG) was constructed by conjugating the anticancer drug Geraniol (GER) to hyaluronic acid (HA) via a disulfide bond. The HSSG NPs displayed a uniform spherical shape with an average diameter of similar to 110 nm, maintained high stability, and realized controlled drug release in the tumor microenvironment (pH/glutathione/hyaluronidase). Results of fluorescence microscopy and flow cytometry verified that HSSG NPs were selectively uptaken by human hepatocellular carcinoma cell lines HepG2 and Huh7 via CD44 receptor-mediated internalization. Studies on H22 tumor-bearing mice demonstrate that HSSG NPs could effectively accumulate at the tumor site for a long period. In vitro and in vivo studies show that HSSG NPs significantly promoted the death of cancer cells while reducing the toxicity as compared to GER. Therefore, the HSSG NPs have great potential in the treatment of tumors.
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页数:12
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