In vitro anticancer activity of doxorubicin-loaded gelatin-coated magnetic iron oxide nanoparticles

被引:19
|
作者
Gaihre, Babita [2 ]
Khil, Myung S. [1 ,3 ]
Kim, Hak Y. [1 ,3 ]
机构
[1] Chonbuk Natl Univ, Ctr Healthcare Technol Dev, Chonju 561756, South Korea
[2] Univ Wollongong, Sch Mech Mat & Mechatron Engn, Wollongong, NSW, Australia
[3] Chonbuk Natl Univ, Dept Text Engn, Chonju 561756, South Korea
关键词
magnetic iron oxide; gelatin; surface coating; drug release; cytotoxicity; cell uptake; in vitro anticancer activity; LOCOREGIONAL CANCER-TREATMENT; COLLOIDAL DISPERSION; SURFACE MODIFICATION; INTRACELLULAR UPTAKE; DIFFERENT PARAMETERS; CONTROLLED-RELEASE; DRUG-RELEASE; DELIVERY; ADSORPTION; PARTICLES;
D O I
10.3109/02652048.2011.559286
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Magnetic drug targeting allows accumulation of drug at a defined target site with the help of an external magnetic field. Current research explored uptake and anticancer activity of doxorubicin-loaded gelatin-coated magnetic iron oxide particles (DXR-GIOPs) in order to investigate potential of gelatin-coated iron oxide particles (GIOPs) as a drug carrier in the field of magnetic drug targeting. The in vitro test was done using HeLa cells as a model cell and DXR as a model drug. The cytotoxicity and uptake of GIOPs were also studied and results were compared with that of DXR-GIOPs. The results indicated that GIOPs were not toxic to HeLa cells even at higher concentration of 1.2 mg/mL; however, DXR-GIOPs showed toxicity in time as well as dose-dependent manner. Furthermore, quantitative and qualitative uptake studies showed higher uptake of DXR-GIOPs compared to GIOPs in the identical condition by the cells.
引用
收藏
页码:286 / 293
页数:8
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