介孔二氧化硅
药物输送
纳米颗粒
介孔材料
材料科学
壳体(结构)
磁性纳米粒子
化学工程
药品
纳米技术
毒品携带者
蛋黄
化学
有机化学
复合材料
药理学
催化作用
医学
食品科学
工程类
作者
Yi Teng,Shu Wu,Xia Chen,Lu Bai,Qiuhua Wu,Guolin Zhang
标识
DOI:10.1080/10601325.2024.2380831
摘要
New magnetic yolk-shell mesoporous silica nanoparticles (Fe3O4@V-mSiO2-PNVCL) were prepared by grafting temperature-sensitive amino-terminated poly (N-vinylcaprolactam) (PNVCL-NH2) on the surface of aldehyde-functionalized magnetic mesoporous silica nanoparticles (Fe3O4@V-mSiO2-CHO) through a Schiff base reaction. Various characterizations were used to confirm the structures, and the drug loading and release behaviors were studied. The drug loading was achieved as PNVCL stretched at room temperature and the drug loading content was up to 54.7% due to the large cavities. The encapsulation of drug from leakage in the blood environment was realized as PNVCL collapsed at physiological temperature. The fracture of pH-liable imine bonds in a slightly acidic tumor environment triggered the burst release of cargo. The Fe3O4@V-mSiO2-PNVCL showed super paramagnetic behavior (21.01 emu∙g−1) which could achieve magnetic targeting. The MTT assay confirmed that the nanoparticles exhibited low cytotoxicity. Furthermore, the cellular uptake experiments indicated that DOX-loaded nanoparticles were successfully internalized into cancer cells. Therefore, the composite nanoparticles are ideal choices for drug carriers.
科研通智能强力驱动
Strongly Powered by AbleSci AI