Red blood cell membrane-camouflaged nanocarriers for the delivery of piperlongumine to treat triple-negative breast cancer.

Chenxi Li, Jiaxin Zhang, Xianxian Yao, Yuxin Huang, Yichen Zhang, Wuli Yang
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Abstract

The application of the conventional drugs for triple-negative breast cancer (TNBC) treatment in chemotherapy is limited due to their intrinsic drawbacks such as short drug half-life, lack of tumor selectivity and systemic toxicity. Herein, an effective nanoparticle drug delivery system (NDDS) of red blood cell (RBC) membrane-camouflaged piperlongumine (PL)-loaded iron oxide (Fe3O4) magnetic nanoparticles (Fe3O4-PL@RBC) was rationally designed as an effective drug delivery platform forin vivoTNBC treatment. The Fe3O4-PL@RBC showed considerable cytotoxicity against MDA-MB-231 cells, inducing intracellular accumulation of reactive oxygen species, mitochondrial dysfunction and apoptosis. Furthermore, transcriptomic analyses and western blotting analysis demonstrated that the Fe3O4-PL@RBC induced apoptosis through the inhibition of PI3K/AKT/mTOR pathway and downregulation of Bcl-2 protein. In MDA-MB-231 tumor models, the RBC membrane coating in Fe3O4-PL@RBC effectively prolonged the circulation time and sufficient enrichment at the tumor sites. And the Fe3O4-PL@RBC significantly inhibited tumor growth with good biosafety. This study provides guidance for the rational design of effective Fe3O4-based NDDS for TNBC treatment.

用于输送胡椒明治疗三阴性乳腺癌的红细胞膜伪装纳米载体。
传统化疗药物治疗三阴性乳腺癌(TNBC)由于药物半衰期短、缺乏肿瘤选择性和全身毒性等固有缺陷,在化疗中的应用受到限制。本研究合理设计了一种红血球(RBC)膜伪装的哌氯明(PL)负载氧化铁(Fe3O4)磁性纳米颗粒(Fe3O4-PL@RBC)的有效纳米颗粒给药系统(NDDS),作为TNBC体内治疗的有效给药平台。Fe3O4-PL@RBC对MDA-MB-231细胞表现出相当大的细胞毒性,诱导细胞内活性氧积累、线粒体功能障碍和细胞凋亡。此外,转录组学分析和western blotting分析表明Fe3O4-PL@RBC通过抑制PI3K/AKT/mTOR通路和下调Bcl-2蛋白诱导细胞凋亡。在MDA-MB-231肿瘤模型中,Fe3O4-PL@RBC中的RBC膜包被有效延长了循环时间,并在肿瘤部位充分富集。Fe3O4-PL@RBC对肿瘤生长有明显抑制作用,具有良好的生物安全性。本研究为合理设计有效的fe3o4基NDDS治疗TNBC提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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