Qingyuan People's Hospital, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan, China.
Department of Biomedical Engineering, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China.
Drug Deliv. 2020 Dec;27(1):983-995. doi: 10.1080/10717544.2020.1785581.
To improve synergistic anticancer efficacy and minimize the adverse effects of chemotherapeutic drugs, temozolomide (TMZ) and curcumin (CUR) co-loaded nanostructured lipid carriers (NLCs) were prepared by microemulsion in this study. And the physicochemical properties, drug release behavior, intracellular uptake efficiency, and anticancer effects of TMZ/CUR-NLCs were evaluated. TMZ/CUR-NLCs showed enhanced inhibitory effects on glioma cells compared to single drug loaded NLCs, which may be owing to that the quickly released CUR can sensitize the cancer cells to TMZ. The inhibitory mechanism is a combination of S phase cell cycle arrest associated with induced apoptosis. Notably, TMZ/CUR-NLCs can accumulate at brain and tumor sites effectively and perform a significant synergistic anticancer effect . More importantly, the toxic effects of TMZ/CUR-NLCs on major organs and normal cells at the same therapeutic dosage were not observed. In conclusion, NLCs are promising nanocarriers for delivering dual chemotherapeutic drugs sequentially, showing potentials in the synergistic treatment of tumors while reducing adverse effects both and .
为了提高抗癌协同疗效并最小化化疗药物的不良反应,本研究通过微乳液法制备了替莫唑胺(TMZ)和姜黄素(CUR)共载纳米结构脂质载体(NLCs)。并评价了 TMZ/CUR-NLCs 的理化性质、药物释放行为、细胞内摄取效率和抗癌效果。与单药载 NLCs 相比,TMZ/CUR-NLCs 对神经胶质瘤细胞表现出增强的抑制作用,这可能是由于快速释放的 CUR 可以使癌细胞对 TMZ 敏感。抑制机制是与诱导细胞凋亡相关的 S 期细胞周期阻滞的组合。值得注意的是,TMZ/CUR-NLCs 可以有效地在脑部和肿瘤部位积累,并表现出显著的协同抗癌作用。更重要的是,在相同治疗剂量下,TMZ/CUR-NLCs 对主要器官和正常细胞的毒性作用未被观察到。总之,NLCs 是递呈两种化疗药物的有前途的纳米载体,在协同治疗肿瘤的同时减少不良反应方面具有潜力。