Cancer cell membrane-camouflaged paclitaxel/PLGA nanoparticles for targeted therapy against lung cancer

紫杉醇 A549电池 肺癌 PLGA公司 细胞毒性 体内 药物输送 癌症 医学 癌症研究 癌细胞 细胞 靶向给药 细胞凋亡 药理学 体外 化学 内科学 生物化学 生物 病理 生物技术 有机化学
作者
Jiahan Zhou,Shengli Wan,Yuesong Wu,Haiyang Hu,Yang Liu,Zuyue Liao,Mengyao Xu,Jianming Wu,Qingze Fan
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:177: 117102-117102 被引量:2
标识
DOI:10.1016/j.biopha.2024.117102
摘要

Paclitaxel (PTX) is a first-line drug for the treatment of lung cancer, but its targeting and therapeutic effect are unsatisfactory. Herein, lung cancer cell (A549) membrane biomimetic PTX-loaded poly (lactic-co-glycolic acid) (PLGA) nanoparticles (AM@PTX-NPs) were constructed to eliminate the shortcomings of PTX. The AM@PTX-NPs were successfully prepared with a high drug loading efficiency (10.90±0.06 %). Moreover, transmission electron microscopy, SDS-PAGE, and western blotting proved that AM@PTX-NPs were spherical nanoparticles camouflaged by the A549 cell membrane. Both in vitro and in vivo assays revealed that the AM@PTX-NPs displayed outstanding targeting capacity due to A549 membrane modification. The cytotoxicity experiment showed that the developed biomimetic formulation was able to effectively reduce the proliferation of A549 cells. Moreover, AM@PTX-NPs exhibited a significant tumor growth inhibition rate (73.00 %) with good safety in the tumor-bearing mice, which was higher than that of the PTX-NPs without A549 membrane coating (37.39 %). Overall, the constructed bioinspired vector could provide a novel platform for the PTX delivery and demonstrated a promising strategy for the targeted cancer treatment.
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