Inhibition of growth and metastasis of breast cancer by targeted delivery of 17-hydroxy-jolkinolide B via hyaluronic acid-coated liposomes

被引:27
|
作者
Liu, Dan [1 ]
Zhang, Qi [1 ]
Wang, Jing [1 ]
Guan, Shuang [1 ]
Cai, Defu [1 ]
Liu, Jicheng [1 ]
机构
[1] Qiqihar Med Univ, Inst Med & Drug Res, 333 Bukui St, Qiqihar 161006, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
17-Hydroxy-jolkinolide B; Hyaluronic acid; Liposomes; Targeting drug delivery; RESPONSIVE NANOPARTICLES; ANTITUMOR-ACTIVITY; CELLULAR UPTAKE; JOLKINOLIDE B; CO-DELIVERY; DOXORUBICIN; PACLITAXEL; APOPTOSIS; EFFICACY; RELEASE;
D O I
10.1016/j.carbpol.2020.117572
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hyaluronic acid (HA)-coated liposomes were designed for the targeted delivery of 17-hydroxy-jolkinolide B (HA-Lip-HJB). HA-Lip-HJB had a particle size of 130.8 +/- 1.9 nm, zeta potential of -52.36 +/- 1.91 mV, and encapsulation efficiency of 89.2 +/- 1.5 %. In vitro cell experiments indicated that modification of HA-Lip-HJB increased its cytotoxicity and cellular uptake via CD44 receptor-mediated endocytosis pathway. Of particular importance is that HA-Lip-HJB suppressed cell migration and invasion by inhibiting epithelial-mesenchymal transition (EMT) process. Moreover, the HA-Lip-HJB displayed notable growth inhibition on tumor spheroids. Furthermore, in vivo tissue distribution and anti-tumor experiments carried on BALB/C mice bearing 4T1 tumor indicated that HA-Lip-HJB had strong tumor targeting and tumor suppression abilities. The results also demonstrated that HA-Lip-HJB inhibited tumor cells migration and colonization on the lung. Therefore, HA-Lip-HJB is a promising formulation for metastatic breast cancer therapy.
引用
收藏
页数:10
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