Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer

被引:78
|
作者
Wang, Jing [1 ]
Liu, Dan [1 ]
Guan, Shuang [1 ]
Zhu, Wenquan [2 ]
Fan, Li [1 ]
Zhang, Qi [1 ]
Cai, Defu [1 ]
机构
[1] Qiqihar Med Univ, Inst Med & Drug Res, 333 Bukui St, Qiqihar 161006, Heilongjiang, Peoples R China
[2] Qiqihar Med Univ, Coll Pharm, Qiqihar, Peoples R China
基金
中国国家自然科学基金;
关键词
Liposome; Hyaluronic acid; Honokiol; Breast cancer metastasis; Tumor targeted therapy; PENETRATING PEPTIDES; MULTIDRUG-RESISTANCE; TARGETED DELIVERY; CARBON NANOTUBES; MOLECULAR-WEIGHT; NANOPARTICLES; PACLITAXEL; SUCCINATE; MIGRATION;
D O I
10.1016/j.carbpol.2020.115981
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In an effort to enhance antitumor and anti-metastasis of breast cancer, honokiol (HNK) was encapsulated into hyaluronic acid (HA) modified cationic liposomes (Lip). The prepared HA-Lip-HNK had a spherical shape with a narrow size distribution. The enhanced antitumor efficacy of HA-Lip-HNK was investigated in 4T1 cells in vitro, wherein flow cytometry and confocal microscopy analysis revealed its HA/CD44-mediated greater cellular internalization. As anticipate, the significant cytotoxicity of the HA-Lip-HNK was also observed in 4T1 tumor spheroids. Furthermore, the superior prevention of tumor metastasis by HA-Lip-HNK was verified by in vitro antiinvasion, wound healing and anti-migration assessments, and in vivo bioluminescence imaging in pulmonary metastasis model. Finally, compared with unmodified liposomes, the HA-Lip-HNK exhibited higher tumor accumulation, and achieved a tumor growth inhibition rate of 59.5 %. As a result, the HA-Lip-HNK may serve as a promising tumor-targeted drug delivery strategy for the efficient therapy of metastatic breast cancer.
引用
收藏
页数:10
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