Polymer-Caged Nanobins for Synergistic Cisplatin-Doxorubicin Combination Chemotherapy

被引:200
作者
Lee, Sang-Min
O'Halloran, Thomas V. [1 ]
Nguyen, SonBinh T.
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
PEGYLATED LIPOSOMAL DOXORUBICIN; DNA TOPOISOMERASE-II; BREAST-CANCER; OVARIAN-CANCER; PHASE-II; CIS-DIAMMINEDIAQUAPLATINUM(II) CATION; DELIVERY-SYSTEM; PLATINUM; CARBOPLATIN; RESISTANCE;
D O I
10.1021/ja107333g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multicomponent chemotherapy has increasingly become a strategy of great importance in clinical cancer treatments. However, this type of chemotherapy has not been demonstrated in nanoscale delivery vehicles where two cytotoxic agents can be packaged together, potentially leading to synergistic drug activities. Herein, we present the codelivery of doxorubicin and cisplatin via a single polymer-caged nanobin (PCN) and show that copackaging can yield strong synergy in the efficacy of these agents. Such a PCN comprises a doxorubicin-encapsulated liposomal core protected by a pH-responsive cisplatin prodrug-loaded polymer shell with tunable drug ratios and surface charge potentials. This dual-agent Pt-PCN(DXR) formulation dramatically enhances the overall cytotoxicity of each drug against cancer cells at reduced doses and exhibits higher synergy than combinations of either the free drugs or separately nano-packaged drugs. These results clearly indicate that the polymer-caged nanobin platform can offer new means for building synergy into combination chemotherapy regimens.
引用
收藏
页码:17130 / 17138
页数:9
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