生物相容性
药物输送
阿霉素
癌细胞
纳米技术
药品
靶向给药
氮化硼
化学
材料科学
毒品携带者
药理学
癌症研究
癌症
医学
化疗
外科
有机化学
内科学
作者
Hui Li,Wei Qiao,Yizhe Shen,Huashan Xu,Yuan Fan,Yuxiang Liu,Yadi Lan,Yan Gong,Fuxue Chen,Shini Feng
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-18
卷期号:15 (4): 1269-1269
被引量:7
标识
DOI:10.3390/pharmaceutics15041269
摘要
Boron nitride nanomaterials are being increasingly recognized as vehicles for cancer drug delivery that increase drug loading and control drug release because of their excellent physicochemical properties and biocompatibility. However, these nanoparticles are often cleared rapidly by the immune system and have poor tumor targeting effects. As a result, biomimetic nanotechnology has emerged to address these challenges in recent times. Cell-derived biomimetic carriers have the characteristics of good biocompatibility, long circulation time, and strong targeting ability. Here, we report a biomimetic nanoplatform (CM@BN/DOX) prepared by encapsulating boron nitride nanoparticles (BN) and doxorubicin (DOX) together using cancer cell membrane (CCM) for targeted drug delivery and tumor therapy. The CM@BN/DOX nanoparticles (NPs) were able to target cancer cells of the same type on its own initiative through homologous targeting of cancer cell membranes. This led to a remarkable increase in cellular uptake. In vitro simulation of an acidic tumor microenvironment could effectively promote drug release from CM@BN/DOX. Furthermore, the CM@BN/DOX complex exhibited an excellent inhibitory effect against homotypic cancer cells. These findings suggest that CM@BN/DOX are promising in targeted drug delivery and potentially personalized therapy against their homologous tumor.
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