Cargando…

A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats

PURPOSE: The study reported here was conducted to determine the systemic oral toxicity and to find the no-observed-adverse-effect level of 20 nm positively charged zinc oxide (ZnO(SM20(+))) nanoparticles in Sprague Dawley rats for 90 days. METHODS: For the 90-day toxicity study, the high dose was se...

Descripción completa

Detalles Bibliográficos
Autores principales: Park, Hark-Soo, Kim, Seon-Ju, Lee, Taek-Jin, Kim, Geon-Yong, Meang, EunHo, Hong, Jeong-Sup, Kim, Su-Hyon, Koh, Sang-Bum, Hong, Seung-Guk, Sun, Yle-Shik, Kang, Jin Seok, Kim, Yu-Ri, Kim, Meyoung-Kon, Jeong, Jayoung, Lee, Jong-Kwon, Son, Woo-Chan, Park, Jae-Hak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279754/
https://www.ncbi.nlm.nih.gov/pubmed/25565829
http://dx.doi.org/10.2147/IJN.S57927
_version_ 1782350752985907200
author Park, Hark-Soo
Kim, Seon-Ju
Lee, Taek-Jin
Kim, Geon-Yong
Meang, EunHo
Hong, Jeong-Sup
Kim, Su-Hyon
Koh, Sang-Bum
Hong, Seung-Guk
Sun, Yle-Shik
Kang, Jin Seok
Kim, Yu-Ri
Kim, Meyoung-Kon
Jeong, Jayoung
Lee, Jong-Kwon
Son, Woo-Chan
Park, Jae-Hak
author_facet Park, Hark-Soo
Kim, Seon-Ju
Lee, Taek-Jin
Kim, Geon-Yong
Meang, EunHo
Hong, Jeong-Sup
Kim, Su-Hyon
Koh, Sang-Bum
Hong, Seung-Guk
Sun, Yle-Shik
Kang, Jin Seok
Kim, Yu-Ri
Kim, Meyoung-Kon
Jeong, Jayoung
Lee, Jong-Kwon
Son, Woo-Chan
Park, Jae-Hak
author_sort Park, Hark-Soo
collection PubMed
description PURPOSE: The study reported here was conducted to determine the systemic oral toxicity and to find the no-observed-adverse-effect level of 20 nm positively charged zinc oxide (ZnO(SM20(+))) nanoparticles in Sprague Dawley rats for 90 days. METHODS: For the 90-day toxicity study, the high dose was set as 500 mg per kg of body weight (mg/kg) and the middle and low dose were set to 250 mg/kg and 125 mg/kg, respectively. The rats were held for a 14-day recovery period after the last administration, to observe for the persistence or reduction of any toxic effects. A distributional study was also carried out for the systemic distribution of ZnO(SM20(+)) NPs. RESULTS: No rats died during the test period. There were no significant clinical changes due to the test article during the experimental period in functional assessment, body weight, food and water consumption, ophthalmological testing, urine analysis, necropsy findings, or organ weights, but salivation was observed immediately after administration in both sexes. The total red blood cell count was increased, and hematocrit, albumin, mean cell volume, mean cell hemoglobin, and mean cell hemoglobin concentration were decreased significantly compared with control in both 500 mg/kg groups. Total protein and albumin levels were decreased significantly in both sexes in the 250 and 500 mg/kg groups. Histopathological studies revealed acinar cell apoptosis in the pancreas, inflammation and edema in stomach mucosa, and retinal atrophy of the eye in the 500 mg/kg group. CONCLUSION: There were significant parameter changes in terms of anemia in the hematological and blood chemical analyses in the 250 and 500 mg/kg groups. The significant toxic change was observed to be below 125 mg/kg, so the no-observed-adverse-effect level was not determined, but the lowest-observed-adverse-effect level was considered to be 125 mg/kg in both sexes and the target organs were found to be the pancreas, eye, and stomach.
format Online
Article
Text
id pubmed-4279754
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-42797542015-01-06 A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats Park, Hark-Soo Kim, Seon-Ju Lee, Taek-Jin Kim, Geon-Yong Meang, EunHo Hong, Jeong-Sup Kim, Su-Hyon Koh, Sang-Bum Hong, Seung-Guk Sun, Yle-Shik Kang, Jin Seok Kim, Yu-Ri Kim, Meyoung-Kon Jeong, Jayoung Lee, Jong-Kwon Son, Woo-Chan Park, Jae-Hak Int J Nanomedicine Original Research PURPOSE: The study reported here was conducted to determine the systemic oral toxicity and to find the no-observed-adverse-effect level of 20 nm positively charged zinc oxide (ZnO(SM20(+))) nanoparticles in Sprague Dawley rats for 90 days. METHODS: For the 90-day toxicity study, the high dose was set as 500 mg per kg of body weight (mg/kg) and the middle and low dose were set to 250 mg/kg and 125 mg/kg, respectively. The rats were held for a 14-day recovery period after the last administration, to observe for the persistence or reduction of any toxic effects. A distributional study was also carried out for the systemic distribution of ZnO(SM20(+)) NPs. RESULTS: No rats died during the test period. There were no significant clinical changes due to the test article during the experimental period in functional assessment, body weight, food and water consumption, ophthalmological testing, urine analysis, necropsy findings, or organ weights, but salivation was observed immediately after administration in both sexes. The total red blood cell count was increased, and hematocrit, albumin, mean cell volume, mean cell hemoglobin, and mean cell hemoglobin concentration were decreased significantly compared with control in both 500 mg/kg groups. Total protein and albumin levels were decreased significantly in both sexes in the 250 and 500 mg/kg groups. Histopathological studies revealed acinar cell apoptosis in the pancreas, inflammation and edema in stomach mucosa, and retinal atrophy of the eye in the 500 mg/kg group. CONCLUSION: There were significant parameter changes in terms of anemia in the hematological and blood chemical analyses in the 250 and 500 mg/kg groups. The significant toxic change was observed to be below 125 mg/kg, so the no-observed-adverse-effect level was not determined, but the lowest-observed-adverse-effect level was considered to be 125 mg/kg in both sexes and the target organs were found to be the pancreas, eye, and stomach. Dove Medical Press 2014-12-15 /pmc/articles/PMC4279754/ /pubmed/25565829 http://dx.doi.org/10.2147/IJN.S57927 Text en © 2014 Park et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Park, Hark-Soo
Kim, Seon-Ju
Lee, Taek-Jin
Kim, Geon-Yong
Meang, EunHo
Hong, Jeong-Sup
Kim, Su-Hyon
Koh, Sang-Bum
Hong, Seung-Guk
Sun, Yle-Shik
Kang, Jin Seok
Kim, Yu-Ri
Kim, Meyoung-Kon
Jeong, Jayoung
Lee, Jong-Kwon
Son, Woo-Chan
Park, Jae-Hak
A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title_full A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title_fullStr A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title_full_unstemmed A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title_short A 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in Sprague Dawley rats
title_sort 90-day study of sub-chronic oral toxicity of 20 nm positively charged zinc oxide nanoparticles in sprague dawley rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279754/
https://www.ncbi.nlm.nih.gov/pubmed/25565829
http://dx.doi.org/10.2147/IJN.S57927
work_keys_str_mv AT parkharksoo a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimseonju a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT leetaekjin a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimgeonyong a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT meangeunho a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT hongjeongsup a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimsuhyon a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kohsangbum a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT hongseungguk a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT sunyleshik a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kangjinseok a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimyuri a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimmeyoungkon a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT jeongjayoung a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT leejongkwon a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT sonwoochan a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT parkjaehak a90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT parkharksoo 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimseonju 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT leetaekjin 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimgeonyong 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT meangeunho 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT hongjeongsup 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimsuhyon 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kohsangbum 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT hongseungguk 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT sunyleshik 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kangjinseok 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimyuri 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT kimmeyoungkon 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT jeongjayoung 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT leejongkwon 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT sonwoochan 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats
AT parkjaehak 90daystudyofsubchronicoraltoxicityof20nmpositivelychargedzincoxidenanoparticlesinspraguedawleyrats