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KMID : 0043320160390121682
Archives of Pharmacal Research
2016 Volume.39 No. 12 p.1682 ~ p.1692
Developmental toxicity of intravenously injected zinc oxide nanoparticles in rats
Lee Jin-Soo

Yu Wook-Joon
Song Jeong-Ah
Sung Chang-Hyun
Jeong Eun-Ju
Han Ji-Seok
Kim Pil-Je
Jo Eun-Hye
Eom Ik-Chun
Kim Hyun-Mi
Kwon Jung-Taek
Choi Kyung-Hee
Choi Jong-Hye
Kim Hey-Jin
Lee Han-Dule
Park Ju-Young
Jin Seon-Mi
Park Kwang-Sik
Abstract
Recent toxicity studies of zinc oxide nanoparticles by oral administration showed relatively low toxicity, which may be resulted from low bioavailability. So, the intrinsic toxicity of zinc oxide nanoparticles needs to be evaluated in the target organs by intravenous injection for full systemic concentration of the administered dosage. Although the exposure chance of injection route is low compared to oral and/or inhalation route, it is important to see the toxicity with different exposure routes to get better risk management tool. In this study, the effects of zinc oxide nanoparticles on dams and fetuses were investigated in rats after intravenous injection (5, 10, and 20 mg/kg) from gestation day 6 to 20. Two of 20 dams in the 20 mg/kg treatment group died during the treatment period. Hematological examination and serum biochemistry showed dose-dependent toxicity in treated dams. Histopathological analysis of treated dams revealed multifocal mixed cell infiltration and thrombosis in lung, tubular dilation in kidneys, and extramedullary hemopoiesis in liver. Total dead fetuses (post-implantation loss) were increased and the body weight of fetus was decreased in the 20 mg/kg treatment group. Statistical differences in corpora lutea, resorption, placental weight, morphological alterations including external, visceral and skeletal malformations were not observed in treated groups. Based on the data, lowest observed adverse effect level of injection route was suggested to be 5 mg/kg in dams and no observed adverse effect level was suggested to be 10 mg/kg in fetal developmental toxicity.
KEYWORD
Zinc oxide nanoparticles, Rat, Intravenous injection, Developmental toxicity
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