转铁蛋白修饰的多组分负载紫杉醇的β-榄香烯纳米乳增强了抗非小细胞肺癌的治疗。
A multi-component paclitaxel -loaded β-elemene nanoemulsion by transferrin modification enhances anti-non-small-cell lung cancer treatment.
发表日期:2024 Aug 10
作者:
Yunyan Chen, Ziwei Zhang, Rui Xiong, Minna Luan, Zhilei Qian, Qiang Zhang, Shaozhen Wang
来源:
INTERNATIONAL JOURNAL OF PHARMACEUTICS
摘要:
开发了一种通过转铁蛋白修饰的多组分紫杉醇 (PTX) 负载 β-榄香烯纳米乳 (Tf-PE-MEs),以增强非小细胞肺癌 (NSCLC) 的治疗。转铁蛋白修饰后,Tf-PE-MEs的粒径为(14.87±1.84)nm,zeta电位为(-10.19±0.870)mV。体外实验表明,Tf-PE-MEs可诱导A549细胞大量凋亡,表明其对A549细胞具有显着的细胞毒性。通过转铁蛋白修饰,Tf-PE-MEs 与 A549 细胞表面过表达的转铁蛋白受体 (TfR) 一起在肿瘤部位有效积累。这将增加靶细胞中 PTX 和 β-榄香烯的浓度,从而增强治疗效果。与单独使用 PTX 相比,Tf-PE-ME 在体内研究中表现出良好的抗肿瘤功效并降低了全身毒性。该研究具有良好的治疗潜力,为非小细胞肺癌的联合抗癌治疗提供了新策略。版权所有©2024。Elsevier B.V.出版。
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.Copyright © 2024. Published by Elsevier B.V.