CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety & CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Beijing 100190, China.
Department of Thoracic Surgery, General Hospital of the Chinese People's Liberation Army, Beijing, 100853, China and Department of Thoracic Surgery, Rocket Force Characteristic Medical Center of the Chinese People's Liberation Army, Beijing, 100088, China.
Nanoscale. 2019 Nov 7;11(41):19520-19528. doi: 10.1039/c9nr05791a. Epub 2019 Oct 1.
The therapeutic efficacy of anti-cancer nanomedicines is generally constrained due to limited accumulation in the solid tumors. In this study, we developed a biomimetic nano-carrier to enhance the chemo-therapeutic efficacy of doxorubicin and icotinib in a chemo-resistant non-small cell lung cancer (NSCLC) cell line harboring a mutation in the epidermal growth factor receptor (EGFR). The unique nanomedicine was prepared by coating with targeting cancer cell membrane proteins as highly specific ligands. The resulting biomimetic nanoparticles were highly stable and exhibited superior homologous targeting ability in vitro compared with control groups. In a mouse EGFR-mutated NSCLC xenograft model, intravenous injection of the biomimetic nanomedicine led to a high tumour inhibition rate (87.56%). Histopathological analysis demonstrated that the biomimetic nanomedicine had minimal side effects. Taken together, a cancer cell membrane-based biomimetic drug carrier can significantly enhance drug accumulation and improve therapeutic efficacy in cancers.
抗癌纳米药物的治疗效果通常受到在实体瘤中有限积累的限制。在这项研究中,我们开发了一种仿生纳米载体,以增强携带表皮生长因子受体(EGFR)突变的化疗耐药非小细胞肺癌(NSCLC)细胞系中阿霉素和伊可替尼的化疗疗效。这种独特的纳米药物是通过用靶向癌细胞膜蛋白作为高度特异性配体进行涂层制备的。与对照组相比,所得仿生纳米粒子具有高度的稳定性,并表现出优异的同源靶向能力。在 EGFR 突变的 NSCLC 小鼠异种移植模型中,静脉注射仿生纳米药物可使肿瘤抑制率达到 87.56%。组织病理学分析表明,仿生纳米药物的副作用极小。总之,基于癌细胞膜的仿生药物载体可以显著提高药物在癌症中的积累并提高治疗效果。