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Analysis of Pulmonary Surfactant after Intratracheal Instillation of SWNCT and MWCNT

SWCNT 및 MWCNT의 기관내 점적주입 후 폐 계면활성제의 분석

  • Lee, Byeongwoo (Risk Assessment Division, Environmental Health Research Department, National Institute of Environmental Research) ;
  • Seo, Jungkwan (Risk Assessment Division, Environmental Health Research Department, National Institute of Environmental Research) ;
  • Shim, Ilseob (Risk Assessment Division, Environmental Health Research Department, National Institute of Environmental Research) ;
  • Eom, Igchun (Risk Assessment Division, Environmental Health Research Department, National Institute of Environmental Research) ;
  • Kim, Plije (Risk Assessment Division, Environmental Health Research Department, National Institute of Environmental Research)
  • 이병우 (국립환경과학원 환경건강연구부 위해성평가연구과) ;
  • 서정관 (국립환경과학원 환경건강연구부 위해성평가연구과) ;
  • 심일섭 (국립환경과학원 환경건강연구부 위해성평가연구과) ;
  • 엄익춘 (국립환경과학원 환경건강연구부 위해성평가연구과) ;
  • 김필제 (국립환경과학원 환경건강연구부 위해성평가연구과)
  • Received : 2017.07.10
  • Accepted : 2017.08.01
  • Published : 2017.08.28

Abstract

Objectives: Carbon nanotubes (CNTs) are next-generation industrial nanoparticles which possess excellent mechanical strength along with good thermal conductivity and electric properties. Given these characteristics, carbon nanotubes are being widely applied in various fields, including research and development. However, concerns have been raised over hazardous properties due to their similar fiber shape to asbestos. Recent studies have shown that CNTs pose potential hazards which may cause fibrosis and/or lung inflammation similarly to asbestos. Methods: After intratracheal instillation of SWCNTs and MWCNTs to rats, pulmonary surfactant (PS) of the SWCNTs and MWCNTs was measured and analyzed using bronchoalveolar lavage fluid collected from the lung. After a single intratracheal instillation of SWCNTs and MWCNTs, phospholipid predominantly showed a significant increase compared to the control group, while proteins exhibited a significant increase both three days and one week after instillation. Results: As a result of surface tension, MWCNTs showed a significant decrease three days after treatment compared to the control group. In the case of the total cell number three days after instillation, MWCNTs revealed a temporarily significant increase when compared to the control group. For PMN number, when compared to the control group, SWCNTs displayed a significant increase throughout the observation period, while MWCNTs showed a significant increase three days and three months after treatment. Conclusions: After exposure to CNTs, the total cell number and PNT number, which indicate inflammatory response, were significantly increased. Therefore, this study suggests fiber-shaped CNTs may have a harmful effect on the lungs.

Keywords

References

  1. Maynard AD. Nanotechnology: the next big thing, or much ado about nothing?. Ann Occup Hyg. 2007; 51: 1-12.
  2. Oh KH, and Lee HS. Standardization trends and technologies for carbon nanotubes. JIES. 2009; 12(4): 20-25.
  3. Aiso S, Yamazaki K, Umeda Y, Asakura M, Kasai T, Takaya T, et al. Pulmonary toxicity of intratracheally instilled multiwall carbon nanotubes in male Fischer 344 rats. Ind Health. 2010; 48: 783-95. https://doi.org/10.2486/indhealth.MS1129
  4. DeLorme MP, Muro Y, Toshihiro Arai T, Banas DA, Frame SR, Reed KL, et al. Ninety-day inhalation toxicity study with a vapor grown carbon nanofiber in rats. Toxicol Sci. 2012; 128: 449-60. https://doi.org/10.1093/toxsci/kfs172
  5. Ma-Hock, Treumann S, Strauss V, Brill S, Luizi F, Mertler, et al. Inhalation toxicity of multi-wall carbon nanotubes in rats exposed for three month. Toxicol Sci. 2009; 112: 468-81. https://doi.org/10.1093/toxsci/kfp146
  6. Mitchell LA, Gao J, Wal RV, Giqliotti A, Burchiel SW, McDonald JD. Pulmonary and systemic immune response to inhaled multiwalled carbon nanotubes. Toxicol Sci. 2007; 100: 203-14. https://doi.org/10.1093/toxsci/kfm196
  7. Muller J, Delos M, Panin N, Rabolli V, Huaux F, Lison D. Absence of carcinogenic response to multiwall carbon nanotubes in a 2-year bioassay in the peritoneal cavity of the rat. Toxicol Sci. 2009; 110: 442.8. https://doi.org/10.1093/toxsci/kfp100
  8. Pauluhn J. Subchronic 13week inhalation exposure of rats to multiwalled carbon nanotubes: toxic effects are determined by density of agglomerate structures, not fibrillar structures. Toxicol Sci. 2010; 113: 226.42. https://doi.org/10.1093/toxsci/kfp247
  9. Lam CW, James JT, McCluskey R, Hunter RL. Pulmonary toxicity of single-wall carbon nanotubes in mice 7 and 90days after intratracheal instillation. Toxicol Sci. 2004; 77(1): 126-34. https://doi.org/10.1093/toxsci/kfg243
  10. Guang Jia, Haifang Wang, Lei Yan, Xiang Wang, Rongjuan Pei, Tao Yan, et al. Cytotoxicity of carbon nanomaterials: Single-wall nanotube, multi-wall nanotube, and fullerene. Environ Sci Technol. 2005; 39(5): 1378-83. https://doi.org/10.1021/es048729l
  11. Nakanishi J. Risk assessment of manufactured nanomaterials: Approaches- overview of approaches and results. Final report issued on August 17, NEDO Project (P06041) 'Research and development of nanoparticle characterization methods' 2011.
  12. Kobayashi N, Naya M, Ema M, Endoh S, Maru J, Mizuno K, et al. Biological response and morphological assessment of individually dispersed multiwall carbon nanotubes in the lung after intratracheal instillation in rats. Toxicology. 2010; 276: 143.53. https://doi.org/10.1016/j.tox.2010.07.021
  13. Morimoto Y, Hirohashi M, Ogami A, Oyabu T, Myojo T, Todoroki M, et al. Pulmonary toxicity of well-dispersed multi-wall carbon nanotubes following inhalation and intratracheal instillation. Nanotoxicology. 2011; 6: 587.99.
  14. Schleh C, Hohlfeld JM. Interaction of nanoparticles with the pulmonary surfactant system. Inhal Toxicol. 2009; 21: 97.103. https://doi.org/10.1080/08958370903005744
  15. Kadoya C, Ogami A, Morimoto Y, Myojo T, Oyabu T, Nishi K, et al. Analysis of bronchoalveolar lavage fluid adhering to lung surfactant. Ind Health. 2012; 50: 31.6. https://doi.org/10.2486/indhealth.MS1253
  16. Choi YS. The use of artificial pulmonary surfactant in neonatal respiratory distress. J Korean Med Assoc. 2015;5 8(4): 330-335.
  17. Na JO, Oh MH, Choi JS, Seo KH, Kim YH. Association between the human surfactant protein-A(SPA) gene locus and chronic obstructive pulmonary diesea in korean population. Tuberc Respir Dis. 2006; 60(6): 638-644. https://doi.org/10.4046/trd.2006.60.6.638
  18. Shvedova AA, Kisin ER, Mercer R, Murray AR, Johnson VJ, Potapovich AI, et al. Unusual inflammatory and fibrogenic pulmonary responses to single walled carbon nanotubes in mice. Am J Physiol Lung Cell Mol Physiol. 2005; 289: 698-708. https://doi.org/10.1152/ajplung.00084.2005
  19. Li JG, Li WX, Xu JY, Cai XQ, Liu RL, Li YJ, et al. Comparative study of pathological lesions induced by multiwalled carbon nanotubes in lungs of mice by intratracheal instillation and inhalation. Environ Toxicol. 2007; 22(4): 415-421. https://doi.org/10.1002/tox.20270
  20. Cunningham, MJ. Gene-cellular interactions of nanomaterials: genotoxicity to genomics in Nanotoxicoloy- Characterization, Dosing and Health Effects (Monteiro-Riviere NA Tran CL., eds.). New York, Informa healthcare. 2007: 173-196.
  21. Muller J, Decordier I, Hoet PH, Lombaert N, Thomassen L, Huaux F, et al. Clastogenic and aneugenic effects of multi-wall carbon nanotubes in epithelial cells. Carcinogenesis. 2008; 29: 427-433. https://doi.org/10.1093/carcin/bgm243
  22. Tanaka Isamu. Evaluating Risks associated with Manufactured Nanomaterials. Developing Toxicity Evaluating Methods by the Inhalation Exposure. 2006-2010.