In vivo treatment of tumors using host-guest conjugated nanoparticles functionalized with doxorubicin and therapeutic gene pTRAIL

被引:89
作者
Fan, Hui [2 ,4 ]
Hu, Qi-Da [3 ,5 ]
Xu, Fu-Jian [1 ]
Liang, Wen-Quan [4 ]
Tang, Gu-Ping [3 ]
Yang, Wan-Tai [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Minist Educ, Key Lab Carbon Fiber & Funct Polymers, Beijing 100029, Peoples R China
[2] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Hangzhou 310016, Zhejiang, Peoples R China
[3] Hangzhou Univ, Inst Chem Biol & Pharmaceut Chem, Hangzhou 310028, Zhejiang, Peoples R China
[4] Zhejiang Univ, Coll Pharmaceut Sci, Dept Pharmaceut, Hangzhou 310058, Zhejiang, Peoples R China
[5] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Gen Surg, Hangzhou 310031, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA; Gene therapy; Vectors; Doxorubicin; pTRAIL; CO-DELIVERY; SUPRAMOLECULAR CHEMISTRY; BETA-CYCLODEXTRIN; CANCER-CELLS; APOPTOSIS; DRUG; CHEMOTHERAPY; COMBINATION; PACLITAXEL; TRAIL;
D O I
10.1016/j.biomaterials.2011.10.043
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The combination of gene therapy and chemotherapy may increase the therapeutic efficacy in the treatment of patients. In this work, the anti-cancer drug Dox and therapeutic gene pTRAIL-loaded host-guest co-delivery system was assayed for the possibility of in vivo synergistically treating tumors. The introduced Dox could act as an auxiliary component to human tumor necrosis factor-related apoptosis-inducing ligand-encoding plasmid gene pTRAIL. Such delivery system possessed the good ability of in vivo retention of chemotherapeutic drugs, achieved good therapeutic effects in the inhibition of tumor growth and significantly prolonged the survival time of tumor-bearing mice. With the efficient ability to co-deliver drug and gene, such host guest assembly should have great potential applications in cancer therapy. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1428 / 1436
页数:9
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