Multicompartmentalized vesosomes containing DOX loaded liposomes and 5FU loaded liposomes for synergistic tumor treatment

被引:19
|
作者
Zhang, Xunan [1 ]
Zong, Wei [1 ]
Wang, Jialiang [2 ,3 ]
Dong, Mingdong [4 ]
Cheng, Wenlong [5 ]
Sun, Tianmeng [2 ,3 ]
Han, Xiaojun [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, State Key Lab Urban Water Resource & Environm, 92 West Da Zhi St, Harbin 150001, Heilongjiang, Peoples R China
[2] Jilin Univ, Hosp 1, 71 Xin Min St, Changchun, Jilin, Peoples R China
[3] Jilin Univ, Inst Immunol, Int Ctr Future Sci, 71 Xin Min St, Changchun, Jilin, Peoples R China
[4] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Gustav Wieds Vej 14, DK-8000 Aarhus, Denmark
[5] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
基金
中国国家自然科学基金;
关键词
PH-SENSITIVE LIPOSOMES; DRUG-RELEASE; DELIVERY; COMBINATION; VESICLES;
D O I
10.1039/c9nj00238c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first priority of drug combination therapy in the treatment of cancer is to achieve enhanced therapeutic efficacy and reduced side effects. The main issue in drug combination therapy is the inscrutable interaction between different drug components. Herein, we developed a multicompartmentalized architecture as a new delivery system. A host liposome encapsulates multiple guest liposomes, where various drug components were loaded into disparate compartments separately. This strategy avoids the interaction among different components before their arrival at the targeting sites and provides the fixed drug combination ratio as needed. Doxorubicin (DOX) and 5-fluorouacil (5FU) loaded smaller liposomes were encapsulated into bigger liposomes with a fixed dose ratio of DOX to 5FU. In vivo tumor growth inhibition by vesosomes was evaluated in HeLa tumor-bearing nude mice, which confirms the enhancement of the delivery system on the synergism of the drug combination.
引用
收藏
页码:4895 / 4899
页数:5
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