紫杉醇
转铁蛋白受体
细胞毒性
A549电池
体内
转铁蛋白
药理学
体外
癌症
肺癌
化学
癌症研究
医学
内科学
生物
生物化学
细胞凋亡
生物技术
作者
Yunyan Chen,Ziwei Zhang,Rui Xiong,Luan Mao-tian,Zhilei Qian,Qian Zhang,Shaozhen Wang
标识
DOI:10.1016/j.ijpharm.2024.124570
摘要
A multi-component paclitaxel (PTX) -loaded β-elemene nanoemulsion by transferrin modification (Tf-PE-MEs) was developed to enhance non-small-cell lung cancer (NSCLC) treatment. After transferrin modification, the particle size of Tf-PE-MEs was (14.87 ± 1.84) nm, and the zeta potential was (-10.19 ± 0.870) mV, respectively. In vitro experiments showed that Tf-PE-MEs induced massive apoptosis in A549 cells, indicating that it had significant cytotoxicity to A549 cells. Through transferrin modification, Tf-PE-MEs accumulated at the tumor site efficiently with overexpressed transferrin receptor (TfR) on the surface of A549 cells. This will allow increasing PTX and β-elemene concentration in the target cells, enhancing the therapeutic effect. Compared to PTX alone, Tf-PE-MEs displayed good anti-tumor efficacy and diminished systemic toxicity in vivo studies. With favourable therapeutic potential, this study provides a new strategy for the combined anticancer treatment of non-small cell lung cancer.
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