Controllable Drug Delivery by Na plus /K plus ATPase α1 Targeting Peptide Conjugated DSPE-PEG Nanocarriers for Breast Cancer

被引:5
|
作者
Yang, Yayan [1 ]
Feng, Qian [1 ]
Ding, Chuanfeng [2 ]
Kang, Wei [3 ,4 ]
Xiao, Xiufeng [1 ]
Yu, Yongsheng [2 ]
Zhou, Qian [2 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fuzhou 350007, Fujian, Peoples R China
[2] Tongji Univ, Shanghai Matern & Infant Hosp 1, Clin & Translat Res Ctr, Sch Med, Shanghai 201204, Peoples R China
[3] Dalian Univ Technol, Sch Bioengn, Dalian, Liaoning, Peoples R China
[4] Dalian Univ Technol, Ningbo Inst, Ningbo, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; NKA-alpha; 1; epirubicin; targeted therapy; peptide; NANOPARTICLES; INTERFERENCE; LIPOSOMES; RELEASE; OUABAIN; CELLS;
D O I
10.1177/15330338211027898
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although Epirubicin (EPI) is a commonly used anthracycline for the treatment of breast cancer in clinic, the serious side effects limit its long-term administration including myelosuppression and cardiomyopathy. Nanomedicines have been widely utilized as drug delivery vehicles to achieve precise targeting of breast cancer cells. Herein, we prepared a DSPE-PEG nanocarrier conjugated a peptide, which targeted the breast cancer overexpression protein Na+/K+ ATPase alpha 1 (NKA-alpha 1). The nanocarrier encapsulated the EPI and grafted with the NKA-alpha 1 targeting peptide through the click reaction between maleimide and thiol groups. The EPI was slowly released from the nanocarrier after entering the breast cancer cells with the guidance of the targeting NKA-alpha 1 peptide. The precise and controllable delivery and release of the EPI into the breast cancer cells dramatically inhibited the cells proliferation and migration in vitro and suppressed the tumor volume in vivo. These results demonstrate significant prospects for this nanocarrier as a promising platform for numerous chemotherapy drugs.
引用
收藏
页码:1 / 8
页数:8
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