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Acute Pulmonary Toxicity and Body Distribution of Inhaled Metallic Silver Nanoparticles
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  • Acute Pulmonary Toxicity and Body Distribution of Inhaled Metallic Silver Nanoparticles
  • Acute Pulmonary Toxicity and Body Distribution of Inhaled Metallic Silver Nanoparticles
저자명
Kwon. Jung-Taek,Minai-Tehrani. Arash,Hwang. Soon-Kyung,Kim. Ji-Eun,Shin. Ji-Young,Yu. Kyeong-Nam,Chang. Seung-Hee,Kim. Dae-Seong
간행물명
Toxicological research
권/호정보
2012년|28권 1호|pp.25-31 (7 pages)
발행정보
한국독성학회
파일정보
정기간행물|ENG|
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기타
이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

The purpose of this study was to determine the acute pulmonary toxicity of metallic silver nanoparticles (MSNPs, 20.30 nm in diameter). Acute pulmonary toxicity and body distribution of inhaled MSNPs in mice were evaluated using a nose-only exposure chamber (NOEC) system. Bronchoalveolar lavage (BAL) fluid analysis, Western blotting, histopathological changes, and silver burdens in various organs were determined in mice. Mice were exposed to MSNPs for 6 hrs. The mean concentration, total surface area, volume and mass concentrations in the NOEC were maintained at $1.93{ imes}10^7$ particles/$cm^3$, $1.09{ imes}10^{10};nm^2/cm^3$, $2.72{ imes}10^{11};nm^3/cm^3$, and 2854.62 ${mu}g/m^3$, respectively. Inhalation of MSPNs caused mild pulmonary toxicity with distribution of silver in various organs but the silver burdens decreased rapidly at 24-hrs post-exposure in the lung. Furthermore, inhaled MSNPs induced activation of mitogen-activated protein kinase (MAPK) signaling in the lung. In summary, single inhaled MSNPs caused mild pulmonary toxicity, which was associated with activated MAPK signaling. Taken together, our results suggest that the inhalation toxicity of MSNPs should be carefully considered at the molecular level.