Acute toxicity and oxidative damage induced by silica nanorattle in vivo

被引:17
作者
Fu ChangHui [1 ,2 ]
Liu TianLong [1 ]
Tang FangQiong [1 ]
Chen Dong [1 ]
Li LinLin [1 ]
Liu HuiYu [1 ]
Li XiaoMin [2 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Lab Controllable Preparat & Applicat Nanomat, Beijing 100190, Peoples R China
[2] Southwest Univ, Sch Anim Sci & Technol, Chongqing 400715, Peoples R China
来源
CHINESE SCIENCE BULLETIN | 2012年 / 57卷 / 20期
基金
中国国家自然科学基金;
关键词
silica nanorattle; acute toxicity; oxidative stress; superoxide dismutase; STRESS; LIVER; NANOPARTICLES; DOXORUBICIN; RESPONSES; DELIVERY; THERAPY;
D O I
10.1007/s11434-012-5187-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hollow mesoporous nanomaterial is a kind of promising new drug delivery system due to their unique hollow structures. In order to evaluate the toxicity of silica nanorattle (SN) particles in vivo, 40 female mice were used in this study to investigate the acute toxicity and oxidative damage. Mice were intravenously injected with SN suspension in sterile 5% glucose at 40, 80 and 240 mg/kg, respectively. The control group was administrated with equal-volume 5% glucose. Weight, feed intake, hematology analysis, blood biochemical assay and histopathology diagnosis were examined. The activities of SOD, GSH and CAT were measured as well. The results demonstrated that the levels of ALT and AST in the mice treated with 240 mg/kg SN increased significantly as compared with the control group (P < 0.05), whereas the contents of BUN and CREA changed unremarkably. The activity of SOD induced by SN in the liver decreased significantly (P < 0.05). In summary, this study revealed that liver was the target organ of the SN. It also can be concluded that activity of SOD played an important role in liver injury caused by SN.
引用
收藏
页码:2525 / 2532
页数:8
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