蜂毒肽
材料科学
石墨烯
赫拉
药物输送
纳米技术
生物物理学
细胞凋亡
体外
癌症研究
癌细胞
癌症
生物化学
膜
生物
医学
内科学
作者
Jinxia Qi,Yonghui Chen,Tiantian Xue,Yue Lin,Shiyuan Huang,Shuyan Cao,Xiaona Wang,Yu Su,Zhenkun Lin
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2019-11-12
卷期号:31 (6): 065102-065102
被引量:34
标识
DOI:10.1088/1361-6528/ab5084
摘要
Melittin (MEL), the primary active component of bee venom, has recently emerged as a promising cancer chemotherapeutic agent. However, the instability and rapid degradation of MEL is a significant challenge in practical therapeutic applications. In the present study, graphene oxide (GO)-based magnetic nanocomposites (PEG-GO-Fe3O4) were prepared and adopted as the drug delivery vehicles of MEL, and the anticancer effects of PEG-GO-Fe3O4/MEL complexes on human cervical cancer HeLa cells were studied. PEG-GO-Fe3O4 exhibited a series of unique physical and chemical properties resulting in multiple interactions with MEL, and ultimately the release of MEL. In vitro experiments showed that PEG-GO-Fe3O4/MEL not only distinctly enhanced the inhibition effect on HeLa cells, but also induced pore formation in the cell membrane that ultimately led to cell lysis. In this newly developed drug delivery system, PEGylated GO plays the role of a MEL protector while Fe3O4 nanoparticles act as magnetic responders; therefore active MEL can be released over a long period of time (up to 72 h) and maintain its inhibition effect on HeLa cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI