Zhao Dujuan, Wu Jilian, Li Chuanxiang, Zhang Huiyuan, Li Zhonghao, Luan Yuxia
School of Pharmaceutical Science, Shandong University,44 West Wenhua Road, Jinan, Shandong Province, 250012, PR China.
People's Hospital of Shouguang,1233 Jiankang Road, Weifang, PR China.
Colloids Surf B Biointerfaces. 2017 Jul 1;155:51-60. doi: 10.1016/j.colsurfb.2017.03.056. Epub 2017 Apr 2.
PTX and DOX have different anticancer mechanisms. The combination of the two anticancer drugs could synergically enhance their anticancer effect, but simultaneously accompanied by severe side effects. In the present study, we constructed a mixed micelle system based on redox-sensitive mPEG-SS-PTX and mPEG-SS-DOX conjugate. The drug delivery system has a fixed and high drug loading content of 24.2% (PTX∼14.8% and DOX∼9.4%) with a precise ratio of PTX and DOX to realize the synchronized and controlled release. The mixed micelle has an average size of 93.3nm with a narrow distribution, suitable for passive targeting to tumor tissues by the EPR effect. In vitro release profile and in vitro anticancer results show the mixed micelles have obvious redox-sensitive release properties in reducing environment and have a significant cytotoxicity to A549 and B16 cells. Importantly, in vivo study shows the mixed micelles have no obvious side effect on mice compared to free PTX/DOX samples during the treatment. Therefore, the constructed redox-sensitive mixed micelle is a promising drug delivery system for cancer therapy.
紫杉醇(PTX)和阿霉素(DOX)具有不同的抗癌机制。两种抗癌药物联合使用可协同增强其抗癌效果,但同时伴有严重的副作用。在本研究中,我们构建了一种基于氧化还原敏感型甲氧基聚乙二醇-二硫键-紫杉醇(mPEG-SS-PTX)和甲氧基聚乙二醇-二硫键-阿霉素(mPEG-SS-DOX)共轭物的混合胶束系统。该药物递送系统具有24.2%的固定且高载药量(PTX约14.8%,DOX约9.4%),PTX与DOX比例精确,可实现同步控释。混合胶束平均粒径为93.3nm,分布窄,适合通过增强渗透与滞留(EPR)效应被动靶向肿瘤组织。体外释放曲线和体外抗癌结果表明,混合胶束在还原环境中具有明显的氧化还原敏感释放特性,对A549和B16细胞具有显著的细胞毒性。重要的是,体内研究表明,与游离PTX/DOX样品相比,混合胶束在治疗过程中对小鼠无明显副作用。因此,构建的氧化还原敏感型混合胶束是一种很有前景的癌症治疗药物递送系统。