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Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley rats
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 (Zn[O.sup.AE100[-]]) or positively (Zn...
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Published in: | International Journal of Nanomedicine 2014, Vol.9, p.SS109 |
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creator | Kim, Yu-Ri Park, Jong-Il Lee, Eun Jeong Park, Sung Ha Seong, Nak-won Kim, Jun-Ho Kim, Geon-Yong Meang, Eun-Ho Hong, Jeong-Sup Kim, Su-Hyon Koh, Sang-Bum Kim, Min-Seok Kim, Cheol-Su Kim, Soo-Ki Son, Sang Wook Seo, Young Rok Kang, Boo Hyon Han, Beom Seok An, Seong Soo A Yun, Hyo-In Kim, Meyoung-Kon |
description | 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 (Zn[O.sup.AE100[-]]) or positively (Zn[O.sup.AE100[+]]) 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 Zn[O.sup.AE100(-)] and Zn[O.sup.AE100(+)] 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. |
doi_str_mv | 10.2147/IJN.S57928 |
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The aim of this study is to investigate the toxic effect(s) of 100 nm negatively (Zn[O.sup.AE100[-]]) or positively (Zn[O.sup.AE100[+]]) 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 Zn[O.sup.AE100(-)] and Zn[O.sup.AE100(+)] 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.</description><identifier>ISSN: 1178-2013</identifier><identifier>DOI: 10.2147/IJN.S57928</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Nanoparticles ; Physiological aspects ; Properties ; Zinc oxide</subject><ispartof>International Journal of Nanomedicine, 2014, Vol.9, p.SS109</ispartof><rights>COPYRIGHT 2014 Dove Medical Press Limited</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Kim, Yu-Ri</creatorcontrib><creatorcontrib>Park, Jong-Il</creatorcontrib><creatorcontrib>Lee, Eun Jeong</creatorcontrib><creatorcontrib>Park, Sung Ha</creatorcontrib><creatorcontrib>Seong, Nak-won</creatorcontrib><creatorcontrib>Kim, Jun-Ho</creatorcontrib><creatorcontrib>Kim, Geon-Yong</creatorcontrib><creatorcontrib>Meang, Eun-Ho</creatorcontrib><creatorcontrib>Hong, Jeong-Sup</creatorcontrib><creatorcontrib>Kim, Su-Hyon</creatorcontrib><creatorcontrib>Koh, Sang-Bum</creatorcontrib><creatorcontrib>Kim, Min-Seok</creatorcontrib><creatorcontrib>Kim, Cheol-Su</creatorcontrib><creatorcontrib>Kim, Soo-Ki</creatorcontrib><creatorcontrib>Son, Sang Wook</creatorcontrib><creatorcontrib>Seo, Young Rok</creatorcontrib><creatorcontrib>Kang, Boo Hyon</creatorcontrib><creatorcontrib>Han, Beom Seok</creatorcontrib><creatorcontrib>An, Seong Soo A</creatorcontrib><creatorcontrib>Yun, Hyo-In</creatorcontrib><creatorcontrib>Kim, Meyoung-Kon</creatorcontrib><title>Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley rats</title><title>International Journal of Nanomedicine</title><description>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 (Zn[O.sup.AE100[-]]) or positively (Zn[O.sup.AE100[+]]) 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 Zn[O.sup.AE100(-)] and Zn[O.sup.AE100(+)] 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.</description><subject>Nanoparticles</subject><subject>Physiological aspects</subject><subject>Properties</subject><subject>Zinc oxide</subject><issn>1178-2013</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2014</creationdate><recordtype>report</recordtype><sourceid/><recordid>eNqNy8tuwjAQhWEvQOK64QlG6jpgB3LrDvWitotuYI9GziQa5NiRbUTp0zdIfQBWR_r1HSFWSq5TtSs2n1_f60NWVGk5ElOlijJJpdpOxCyEs5RZUebVVISj-2HN8QauASUl2A5-2WoYck1g0boefWRtKDwDgqfe-XjHlUxqvN0DYaQanEcDWHdsOUSPkZ0FtnDoPbYXgle8Gho4xrAQ4wZNoOX_zsXT-9vx5SNp0dCJbeOGv-446NN-J1Wq8rysto-pP0bjTcM</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Kim, Yu-Ri</creator><creator>Park, Jong-Il</creator><creator>Lee, Eun Jeong</creator><creator>Park, Sung Ha</creator><creator>Seong, Nak-won</creator><creator>Kim, Jun-Ho</creator><creator>Kim, Geon-Yong</creator><creator>Meang, Eun-Ho</creator><creator>Hong, Jeong-Sup</creator><creator>Kim, Su-Hyon</creator><creator>Koh, Sang-Bum</creator><creator>Kim, Min-Seok</creator><creator>Kim, Cheol-Su</creator><creator>Kim, Soo-Ki</creator><creator>Son, Sang Wook</creator><creator>Seo, Young Rok</creator><creator>Kang, Boo Hyon</creator><creator>Han, Beom Seok</creator><creator>An, Seong Soo A</creator><creator>Yun, Hyo-In</creator><creator>Kim, Meyoung-Kon</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20140101</creationdate><title>Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley rats</title><author>Kim, Yu-Ri ; Park, Jong-Il ; Lee, Eun Jeong ; Park, Sung Ha ; Seong, Nak-won ; Kim, Jun-Ho ; Kim, Geon-Yong ; Meang, Eun-Ho ; Hong, Jeong-Sup ; Kim, Su-Hyon ; Koh, Sang-Bum ; Kim, Min-Seok ; Kim, Cheol-Su ; Kim, Soo-Ki ; Son, Sang Wook ; Seo, Young Rok ; Kang, Boo Hyon ; Han, Beom Seok ; An, Seong Soo A ; Yun, Hyo-In ; Kim, Meyoung-Kon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_infotracmisc_A4012166893</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Nanoparticles</topic><topic>Physiological aspects</topic><topic>Properties</topic><topic>Zinc oxide</topic><toplevel>online_resources</toplevel><creatorcontrib>Kim, Yu-Ri</creatorcontrib><creatorcontrib>Park, Jong-Il</creatorcontrib><creatorcontrib>Lee, Eun Jeong</creatorcontrib><creatorcontrib>Park, Sung Ha</creatorcontrib><creatorcontrib>Seong, Nak-won</creatorcontrib><creatorcontrib>Kim, Jun-Ho</creatorcontrib><creatorcontrib>Kim, Geon-Yong</creatorcontrib><creatorcontrib>Meang, Eun-Ho</creatorcontrib><creatorcontrib>Hong, Jeong-Sup</creatorcontrib><creatorcontrib>Kim, Su-Hyon</creatorcontrib><creatorcontrib>Koh, Sang-Bum</creatorcontrib><creatorcontrib>Kim, Min-Seok</creatorcontrib><creatorcontrib>Kim, Cheol-Su</creatorcontrib><creatorcontrib>Kim, Soo-Ki</creatorcontrib><creatorcontrib>Son, Sang Wook</creatorcontrib><creatorcontrib>Seo, Young Rok</creatorcontrib><creatorcontrib>Kang, Boo Hyon</creatorcontrib><creatorcontrib>Han, Beom Seok</creatorcontrib><creatorcontrib>An, Seong Soo A</creatorcontrib><creatorcontrib>Yun, Hyo-In</creatorcontrib><creatorcontrib>Kim, Meyoung-Kon</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Yu-Ri</au><au>Park, Jong-Il</au><au>Lee, Eun Jeong</au><au>Park, Sung Ha</au><au>Seong, Nak-won</au><au>Kim, Jun-Ho</au><au>Kim, Geon-Yong</au><au>Meang, Eun-Ho</au><au>Hong, Jeong-Sup</au><au>Kim, Su-Hyon</au><au>Koh, Sang-Bum</au><au>Kim, Min-Seok</au><au>Kim, Cheol-Su</au><au>Kim, Soo-Ki</au><au>Son, Sang Wook</au><au>Seo, Young Rok</au><au>Kang, Boo Hyon</au><au>Han, Beom Seok</au><au>An, Seong Soo A</au><au>Yun, Hyo-In</au><au>Kim, Meyoung-Kon</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley rats</atitle><jtitle>International Journal of Nanomedicine</jtitle><date>2014-01-01</date><risdate>2014</risdate><volume>9</volume><spage>SS109</spage><pages>SS109-</pages><issn>1178-2013</issn><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 (Zn[O.sup.AE100[-]]) or positively (Zn[O.sup.AE100[+]]) 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 Zn[O.sup.AE100(-)] and Zn[O.sup.AE100(+)] 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.</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/IJN.S57928</doi></addata></record> |
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source | PubMed (Medline); Publicly Available Content Database; Taylor & Francis Open Access Journals |
subjects | Nanoparticles Physiological aspects Properties Zinc oxide |
title | Toxicity of 100 nm zinc oxide nanoparticles: a report of 90-day repeated oral administration in Sprague Dawley rats |
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