介孔二氧化硅
膦酸盐
纳米颗粒
材料科学
细胞毒性T细胞
细胞培养
生物物理学
细胞毒性
成纤维细胞
细胞
纳米技术
介孔材料
化学
体外
生物化学
生物
遗传学
催化作用
作者
Nandita Menon,David Tai Leong
标识
DOI:10.1021/acsami.5b11741
摘要
In this work, we synthesized pristine mesoporous silica nanoparticles (MSN) and functionalized these with phosphonate groups (MSN-Phos). We report, for the first time, cell death in MCF-7 cells (human breast adenocarcinoma cell line) when exposed to the empty MSN and MSN-Phos nanoparticles. In comparison, the same nanoparticles were found to elicit few deleterious effects on normal human foreskin fibroblast cells (BJ cells). MCF-7 cells were found to exhibit a concentration-dependent uptake, whereas no detectable nanoparticle uptake was observed in the BJ cells, irrespective of treatment dosage. A disruption of the cell cycle in the MCF-7 cells was determined to be the cause of cell death from the nanoparticle exposure, thereby suggesting the role of nondrug loaded MSN and MSN-Phos as effective anticancer drugs.
科研通智能强力驱动
Strongly Powered by AbleSci AI