顺铂
医学
细胞毒性
多重耐药
细胞凋亡
齐墩果酸
药理学
化疗
抗药性
细胞内
肺癌
癌症研究
癌症
体外
肿瘤科
内科学
化学
病理
微生物学
生物化学
生物
替代医学
作者
Xiaokai Zhang,Qiwen Wang,Yajuan Xu,Hong‐Mei Sun,Lei Wang,Lixin Zhang
摘要
Multidrug resistance (MDR) of chemotherapy is one of the significant concerns in cancer therapy. Here in our study, cisplatin (DDP) and oleanolic acid (OA) were co-loaded in mesoporous silica nanoparticles (Nsi) to construct DDP/OA-Nsi and solve the DDP-resistance in lung cancer therapy. The cytotoxicity and apoptosis assays demonstrated that in DDP-resistant A549/DDP cells, the cytotoxicity of DDP/OA-Nsi was significantly higher than that of free DDP or DDP single delivery system (DDP-Nsi). The intracellular drug accumulation study revealed that the intracellular DDP concentration in the DDP/OA-Nsi group was also higher than that in free DDP and DDP-Nsi groups. In the A549/DDP xenograft tumor model, DDP/OA-Nsi showed the best anticancer effect. In summary, DDP/OA-Nsi was a promising drug delivery system to solve MDR in lung cancer therapy.
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