RETRACTED: Co-delivery of doxorubicin and SIS3 by folate-targeted polymeric micelles for overcoming tumor multidrug resistance (Retracted Article)

被引:9
作者
Wang, Shuanghu [1 ]
Tan, Xueying [2 ]
Zhou, Quan [1 ]
Geng, Peiwu [1 ]
Wang, Jinhui [3 ]
Zou, Ping [4 ]
Deng, Aiping [4 ]
Hu, Jingbo [1 ,3 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 6, Peoples Hosp Lishui, Lab Clin Pharm, Lishui, Peoples R China
[2] Zhejiang Pharmaceut Coll, Coll Pharm, Ningbo, Peoples R China
[3] Ningbo Univ, Inst Drug Discovery Technol, Ningbo, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Med Coll, Cent Hosp Wuhan, Dept Pharm, Wuhan 430000, Peoples R China
基金
中国国家自然科学基金;
关键词
Multidrug resistance; Doxorubicin; Smad3; inhibitor; SIS3; Folate-targeted micelles; BREAST-CANCER; INHIBITOR; SMAD3; DRUGS; NANOPARTICLES;
D O I
10.1007/s13346-020-00895-1
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Multidrug resistance (MDR) is considered as a critical limiting factor for the successful chemotherapy, which is mainly characterized by the overexpression of ATP-binding cassette (ABC) transporter ABCB1 or ABCG2. In this study, folate-targeted polymeric micellar carrier was successfully constructed to co-delivery of doxorubicin (DOX) and SIS3 (FA/DOX/SIS3 micelles), a specific Smad3 inhibitor which sensitizes ABCB1- and ABCG2-overexpressing cancer cells to chemotherapeutic agents. The ratio of DOX to SIS3 in polymeric micelles was determined based on the anti-tumor activity against resistant breast cells. In addition, FA/DOX/SIS3 micelles exhibited a much longer circulation time in blood and were preferentially accumulated in resistant tumor tissue. Pharmacodynamic studies showed that FA/DOX/SIS3 micelles possessed superior anti-tumor activity than other DOX-based treatments. Overall, FA/DOX/SIS3 micelles are a promising formulation for the synergistic treatment of drug-resistant tumor.
引用
收藏
页码:167 / 179
页数:13
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