三氟拉嗪
介孔二氧化硅
纳米颗粒
介孔有机硅
化学
材料科学
化学工程
介孔材料
纳米技术
有机化学
催化作用
工程类
冶金
钙调蛋白
钙
作者
Yanxing Ma,Longxia Li,Liufang Mo,Xiaochen Wang,C.T. Liu,Yijun Wu,Chaoqun Liu
摘要
We have developed a targeted nano-drug delivery system that effectively harnesses the anti-tumor properties of trifluoperazine (TFP), while concurrently mitigating its side effects on the central nervous system. The manufacturing process entailed the preparation of mesoporous silica nanoparticles (MSN-NH2), followed by the loading of trifluoperazine into the pores of MSN-NH2 and then surface modification with polyethylene glycol (PEG) and anisamide (AA), resulting in the formation of TFP@MSN@PEG-AA (abbreviated as TMPA) nanoparticles. In vitro and in vivo anti-tumor activity and hemolysis experiments showed that TMPA had an excellent safety profile and a good anti-tumor effect. Importantly, the drug content of the TMPA nanoparticle group was found to be significantly lower than that of the TFP group in the mouse brain tissue as determined by High Performance Liquid Chromatography (HPLC) detection. Therefore, the developed drug delivery system achieved the goal of maintaining TFP's anti-tumor action while avoiding its negative effects on the central nervous system.
科研通智能强力驱动
Strongly Powered by AbleSci AI