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Subchronic oral toxicity of silver nanoparticles

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dc.contributor.authorKim, Yong Soon-
dc.contributor.authorSong, Moon Yong-
dc.contributor.authorPark, Jung Duck-
dc.contributor.authorSong, Kyung Seuk-
dc.contributor.authorRyu, Hyeon Ryol-
dc.contributor.authorChung, Yong Hyun-
dc.contributor.authorChang, Hee Kyung-
dc.contributor.authorLee, Ji Hyun-
dc.contributor.authorOh, Kyung Hui-
dc.contributor.authorKelman, Bruce J-
dc.contributor.authorHwang, In Koo-
dc.contributor.authorYu, Il Je-
dc.date.accessioned2017-03-17T06:18:15Z-
dc.date.available2017-03-17T16:25:01Z-
dc.date.issued2010-08-06-
dc.identifier.citationParticle and Fibre Toxicology, 7(1):20ko_KR
dc.identifier.urihttps://hdl.handle.net/10371/109795-
dc.description.abstractBackground
The antibacterial effect of silver nanoparticles has resulted in their extensive application in health, electronic, consumer, medicinal, pesticide, and home products; however, silver nanoparticles remain a controversial area of research with respect to their toxicity in biological and ecological systems.

Results
This study tested the oral toxicity of silver nanoparticles (56 nm) over a period of 13 weeks (90 days) in F344 rats following Organization for Economic Cooperation and Development (OECD) test guideline 408 and Good Laboratory Practices (GLP). Five-week-old rats, weighing about 99 g for the males and 92 g for the females, were divided into four 4 groups (10 rats in each group): vehicle control, low-dose (30 mg/kg), middle-dose (125 mg/kg), and high-dose (500 mg/kg). After 90 days of exposure, clinical chemistry, hematology, histopathology, and silver distribution were studied. There was a significant decrease (P < 0.05) in the body weight of male rats after 4 weeks of exposure, although there were no significant changes in food or water consumption during the study period. Significant dose-dependent changes were found in alkaline phosphatase and cholesterol for the male and female rats, indicating that exposure to more than 125 mg/kg of silver nanoparticles may result in slight liver damage. Histopathologic examination revealed a higher incidence of bile-duct hyperplasia, with or without necrosis, fibrosis, and/or pigmentation, in treated animals. There was also a dose-dependent accumulation of silver in all tissues examined. A gender-related difference in the accumulation of silver was noted in the kidneys, with a twofold increase in female kidneys compared to male kidneys.

Conclusions
The target organ for the silver nanoparticles was found to be the liver in both the male and female rats. A NOAEL (no observable adverse effect level) of 30 mg/kg and LOAEL (lowest observable adverse effect level) of 125 mg/kg are suggested from the present study.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.titleSubchronic oral toxicity of silver nanoparticlesko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김용순-
dc.contributor.AlternativeAuthor송문용-
dc.contributor.AlternativeAuthor박정덕-
dc.contributor.AlternativeAuthor송경석-
dc.contributor.AlternativeAuthor류현렬-
dc.contributor.AlternativeAuthor정용현-
dc.contributor.AlternativeAuthor장희경-
dc.contributor.AlternativeAuthor이지현-
dc.contributor.AlternativeAuthor오경희-
dc.contributor.AlternativeAuthor황인구-
dc.contributor.AlternativeAuthor유일제-
dc.identifier.doi10.1186/1743-8977-7-20-
dc.language.rfc3066en-
dc.rights.holderKim et al; licensee BioMed Central Ltd.-
dc.date.updated2017-01-06T10:32:23Z-
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