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Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley ratsopen access

Authors
Kim, Yu-RiPark, Jong-IlLee, Eun JeongPark, Sung HaSeong, Nak-wonKim, Jun-HoKim, Geon-YongMeang, Eun-HoHong, Jeong-SupKim, Su-HyonKoh, Sang-BumKim, Min-SeokKim, Cheol-SuKim, Soo-KiSon, Sang WookSeo, Young RokKang, Boo HyonHan, Beom SeokAn, Seong Soo A.Yun, Hyo-InKim, Meyoung-Kon
Issue Date
15-Dec-2014
Publisher
DOVE MEDICAL PRESS LTD
Keywords
zinc oxide nanoparticles; surface charge; 90-day oral dose toxicity; no observed adverse effect level
Citation
INTERNATIONAL JOURNAL OF NANOMEDICINE, v.9, pp 109 - 126
Pages
18
Indexed
SCI
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume
9
Start Page
109
End Page
126
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/8633
DOI
10.2147/IJN.S57928
ISSN
1176-9114
1178-2013
Abstract
Nanoparticles (NPs) are used commercially in health and fitness fields, but information about the toxicity and mechanisms underlying the toxic effects of NPs is still very limited. The aim of this study is to investigate the toxic effect(s) of 100 nm negatively (ZnOAE100[-])or positively (ZnOAE100[+]) charged zinc oxide (ZnO) NPs administered by gavage in Sprague Dawley rats, to establish a no observed adverse effect level, and to identify target organ(s). After verification of the primary particle size, morphology, hydrodynamic size, and zeta potential of each test article, we performed a 90-day study according to Organisation for Economic Co-operation and Development test guideline 408. For the 90-day study, the high dose was set at 500 mg/kg and the middle and low doses were set at 125 mg/kg and 31.25 mg/kg, respectively. Both ZnO NPs had significant changes in hematological and blood biochemical analysis, which could correlate with anemia-related parameters, in the 500 mg/kg groups of both sexes. Histopathological examination showed significant adverse effects (by both test articles) in the stomach, pancreas, eye, and prostate gland tissues, but the particle charge did not affect the tendency or the degree of the lesions. We speculate that this inflammatory damage might result from continuous irritation caused by both test articles. Therefore, the target organs for both ZnOAE100(-) and ZnOAE100(+) are considered to be the stomach, pancreas, eye, and prostate gland. Also, the no observed adverse effect level for both test articles was identified as 31.25 mg/kg for both sexes, because the adverse effects were observed at all doses greater than 125 mg/kg.
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College of Medicine (Department of Biochemistry and Molecular Biology)
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