Kiran Sonia, Hai Zijuan, Ding Zhanling, Wang Lin, Liu Yaling, Zhang Huafeng, Liang Gaolin
CAS Key Laboratory of Soft Matter Chemistry, Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, China.
Chem Commun (Camb). 2018 Feb 15;54(15):1853-1856. doi: 10.1039/c7cc09365a.
Etoposide is a cancer-targeting drug but an overdose of etoposide leads to immunosuppression in patients. Therefore, the development of a new strategy to enhance its anticancer effect, while in the meantime alleviating its adverse effects, is important but challenging. In this work, with the assistance of a hydrogelator precursor Nap-Phe-Phe-Tyr(HPO)-OH (1P), etoposide phosphate (EP) was subjected to alkaline phosphatase (ALP)-triggered assembly, which obviously enhanced its anticancer efficacy in vitro and in vivo. In vitro tests indicated that the assembly of EP with 1P resulted in a slow release of etoposide and long-term inhibitory effects on HeLa cells. In vivo experiments indicated that, compared with those of EP-treated mice, the tumor growth of EP + 1P-treated mice was further inhibited while their body weight loss was alleviated. We envision that our hydrogelator-assisted assembly strategy could be applied to enhance the therapeutic effects of more drugs, while in the meantime alleviating their adverse effects in the future.
依托泊苷是一种靶向抗癌药物,但过量使用依托泊苷会导致患者免疫抑制。因此,开发一种新策略来增强其抗癌效果,同时减轻其不良反应,既重要又具有挑战性。在这项工作中,在水凝胶前体Nap-Phe-Phe-Tyr(HPO)-OH(1P)的辅助下,磷酸依托泊苷(EP)进行了碱性磷酸酶(ALP)触发的组装,这明显增强了其在体外和体内的抗癌功效。体外试验表明,EP与1P的组装导致依托泊苷的缓慢释放以及对HeLa细胞的长期抑制作用。体内实验表明,与EP处理的小鼠相比,EP + 1P处理的小鼠肿瘤生长进一步受到抑制,同时体重减轻得到缓解。我们设想,我们的水凝胶辅助组装策略未来可应用于增强更多药物的治疗效果,同时减轻其不良反应。