Effect of surface charge and agglomerate degree of magnetic iron oxide nanoparticles on KB cellular uptake in vitro

被引:148
|
作者
Ge, Yuqing [1 ]
Zhang, Yu [1 ]
Xia, Jingguang [1 ]
Ma, Ming [1 ]
He, Shiying [1 ]
Nie, Fang [2 ]
Gu, Ning [1 ]
机构
[1] Southeast Univ, State Key Lab Bioelect, Jiangsu Lab Biomat & Devices, Sch Biol Sci & Med Engn, Nanjing 210096, Peoples R China
[2] Southeast Univ, Dept Radiol, Zhongda Hosp, Nanjing 210096, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetic iron oxide nanoparticle; Surface charge; Cellular uptake; Chitosan; Magnetic agglomerates; MRI; PARTICLE-SIZE; CELLS; CANCER; CYTOTOXICITY; NANOCRYSTALS; DEPENDENCE; DELIVERY; CHITOSAN; AGENT;
D O I
10.1016/j.colsurfb.2009.05.031
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We synthesized three types of magnetic iron oxide nanoparticles (MNPs), which were meso-2,3-dimercaptosuccinic acid (DMSA) coated MNPs (DMSA@MNPs, 17.3 +/- 4.8 nm, negative charge), chitosan (CS) coated MNPs (CS@MNPs. 16.5 +/- 6.1 nm, positive charge) and magnetic nanoparticles agglomerates, formed by electronic aggregation between DMSA@MNPs and CS (CS-DMSA@MNPs, 85.7 +/- 72.9 nm, positive charge) respectively. The interactions of these MNPs with Oral Squamous Carcinoma Cell KB were investigated. The results showed that cellular uptakes of MNPs were on the dependence of incubation time, nanoparticles concentration and nanoparticles properties such as surface charge, size, etc. The cellular uptake was enhanced with the increase of incubation time and nanoparticles concentration. Although all MNPs could enter to cells, we observed apparent differences in the magnitude of nanoparticles uptaken. The cellular uptake of CS-DMSA@MNPs by KB cells was the highest and that of DMSA@MNPs was the lowest among the three types of MNPs. The same conclusions were drawn via the reduction of water proton relaxation times T(2)*, resulting from the different iron load of labeled cells using a 1.5 T clinical MR imager. The finding of this study will have implications in the chemical design of nanomaterials for biomedical applications. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:294 / 301
页数:8
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