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Toxicity and Clearance of Intratracheally Administered Multiwalled Carbon Nanotubes from Murine Lung

Authors
Kim, Ji-EunLim, Hwang-TaeMinai-Tehrani, ArashKwon, Jung-TaekShin, Ji-YoungWoo, Chang-GyuChoi, MansooBaek, JonghoJeong, Dae HongHa, Yoon-CheolChae, Chan-HeeSong, Kyung-SukAhn, Kang-HoLee, Ji-HyunSung, Ha-JungYu, Il-JeBeck, George R., Jr.Cho, Myung-Haing
Issue Date
Oct-2010
Publisher
TAYLOR & FRANCIS INC
Keywords
CELLS; DNA-DAMAGE; IN-VIVO; TISSUE; NANOMATERIALS; MICE; BIODISTRIBUTION; CYTOTOXICITY; ASBESTOS; EXPOSURE
Citation
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, v.73, no.21-22, pp.1530 - 1543
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES
Volume
73
Number
21-22
Start Page
1530
End Page
1543
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/40551
DOI
10.1080/15287394.2010.511578
ISSN
1528-7394
Abstract
Carbon nanotubes (CNT) are known to have widespread industrial applications; however, several reports indicated that these compounds may be associated with adverse effects in humans. In this study, multiwalled carbon nanotubes were administered to murine lungs intratracheally to determine whether acute and chronic pulmonary toxicity occurred. In particular, pristine multiwalled carbon nanotubes (PMWCNT) and acid-treated multiwalled carbon nanotubes (TMWCNT) were used in this study. In broncheoalveolar lavage fluid (BALF) cell analysis, PMWCNT induced more severe acute inflammatory cell recruitment than TMWCNT. Histopathologically, both PMWCNT and TMWCNT induced multifocal inflammatory granulomas in a dose-dependent manner. The observed granulomas were reversible, with TMWCNT-induced granulomas diminishing faster than PMWCNT-induced granulomas. Although the area of granuloma reduced with time, hyperplasia and dysplastic characteristics such as mitotic figures, anisokaryosis, and anisocytosis were still observed. These findings demonstrate that MWCNT induces granulomatous inflammation, and the duration and pattern of inflammation seem to vary depending upon the types of MWCNT to which mice are exposed. Therefore, toxicity studies on various types of CNT are needed as the responsiveness to these compounds differs.
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