A novel estrogen-targeted PEGylated liposome co-delivery oxaliplatin and paclitaxel for the treatment of ovarian cancer

被引:14
作者
Xie, Yizhuo [1 ]
Ren, Zhihui [1 ]
Chen, Hongyu [1 ]
Tang, Huan [1 ]
Zhu, Ming [1 ]
Lv, Zhe [1 ]
Bao, Han [1 ]
Zhang, Yan [1 ]
Liu, Rui [1 ]
Shen, Yujia [1 ]
Zheng, Yucui [1 ]
Miao, Dongfanghui [1 ]
Guo, Xin [1 ]
Chen, Hongli [1 ]
Wang, Shanshan [1 ]
Pei, Jin [1 ,2 ]
机构
[1] Jilin Univ, Sch Pharmaceut Sci, Dept Biopharm, Changchun, Peoples R China
[2] Jilin Univ, Sch Pharmaceut Sci, 1163 Xinmin St, Changchun 130021, Jilin, Peoples R China
关键词
Ovarian cancer; Estrogen receptor; Combined chemotherapy; Active targeting; Liposome; Anti-tumor efficacy; IN-VITRO; BEVACIZUMAB; RECEPTORS; TRIAL;
D O I
10.1016/j.biopha.2023.114304
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ovarian cancer is the second cause of death among gynecological malignancies. In this study, we designed a novel estrogen-targeted PEGylated liposome loaded with oxaliplatin and paclitaxel (ES-SSL-OXA/PTX) which could target estrogen receptor (ER) highly expressed on the surface of SKOV-3 cells to enhance therapeutic ef-ficacy and reduce the side effects for SKOV-3 tumor therapy. ES-SSL-OXA/PTX was prepared by thin film hy-dration method and exhibited a uniform spherical morphology. Encapsulation efficiency (EE) were determined by HPLC method with the results of 44.10% for OXA and 65.85% for PTX. The mean particle size and poly-dispersity index (PDI) were 168.46 nm and 0.145, respectively. In vivo and in vitro targeting study confirmed that ES-SSL-OXA/PTX has optimum specific targeting ability. Meanwhile, In vitro and in vivo antitumor results of ES-SSL-OXA/PTX exhibited a superior antiproliferative effect on SKOV-3 cells and a stronger anti-tumor efficacy with the tumor inhibition rate of 85.24%. The pharmacokinetics results of ES-SSL-OXA/PTX showed a prolonged half-life time and a slowed clearance rate. The preliminary safety study of acute toxicity and long-term toxicity demonstrated ES-SSL-OXA/PTX exhibited a reduced toxicity profile. Based on the above results, ES-SSL-OXA/ PTX could be a promising novel formulation for the treatment of ovarian cancer in future clinic.
引用
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页数:20
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