Department of Chemistry and the Center of Cancer Nanotechnology Excellence, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA.
J Am Chem Soc. 2010 Dec 8;132(48):17130-8. doi: 10.1021/ja107333g. Epub 2010 Nov 15.
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.
多组分化疗在癌症临床治疗中越来越成为一种重要的策略。然而,这种化疗方法在纳米级递药载体中尚未得到证实,在这些载体中可以将两种细胞毒性药物一起包装,从而可能产生协同的药物活性。在此,我们通过单个聚合物笼纳米盒(PCN)共递给药,展示了共包装可以使这些药物的疗效产生强烈的协同作用。该 PCN 包含一个由 pH 响应性顺铂前药负载的聚合物壳保护的包载多柔比星的脂质体核心,具有可调的药物比例和表面电荷势。这种双药物 Pt-PCN(DXR)制剂在降低剂量的情况下显著提高了每种药物对癌细胞的整体细胞毒性,并表现出比游离药物或单独纳米包装药物的组合更高的协同作用。这些结果清楚地表明,聚合物笼纳米盒平台可以为联合化疗方案提供构建协同作用的新方法。