Stoker Emily, Purser Forrest, Kwon Soonjo, Park Young-Bin, Lee Joon Sang
Department of Biological Engineering, Utah State University, 4105 Old Main Hill, Logan, UT 84322-4105, USA.
Int J Toxicol. 2008 Nov;27(6):441-8. doi: 10.1080/10915810802552138.
Recent discoveries of various forms of carbon nanostructure have stimulated research on their applications and hold promise for applications in medicine and other related engineering areas. Although carbon nanotubes (CNTs) are already being produced on a massive scale, few studies have been performed which test the potential harmful effects of this new technology. The authors used a three-dimensional in vitro model of the human airway using a coculture of normal human bronchial epithelial cells and normal human fibroblasts for the health risk assessment of CNTs on the human respiratory systems. The authors used aqueous single-walled carbon nanotube (SWCNT) solution. The average length and diameter of nanotube ropes were about 500 nm and less than 10 nm, respectively. The authors measured the production of nitric oxide (NO) as an inflammatory marker and mitochondrial activity using MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay as a cytotoxic response of the cell layers following exposure of different concentration of aqueous SWCNT solution. The results indicated that NO production was dramatically increased and cell viability was decreased following exposure of different concentrations of SWCNTs. Transepithelial electrical resistance (TER) across the coculture layers was measured to observe the changes in airway physiological function following exposure of different concentrations of SWCNTs. TER value was dramatically decreased following exposure of 20% SWCNT (8 microg/ml). In this study, the authors presented viable alternatives to in vivo tests to evaluate the toxicity of engineered SWCNTs. Cytotoxic/inflammatory responses and barrier function of the human lung layers following exposure of SWCNTs were observed using in vitro coculture system of airway.
近期各种形式碳纳米结构的发现激发了对其应用的研究,并有望应用于医学及其他相关工程领域。尽管碳纳米管(CNTs)已实现大规模生产,但很少有研究测试这项新技术的潜在有害影响。作者使用正常人支气管上皮细胞和正常人成纤维细胞的共培养体系,构建了人呼吸道的三维体外模型,以评估碳纳米管对人体呼吸系统的健康风险。作者使用了水性单壁碳纳米管(SWCNT)溶液。纳米管束的平均长度和直径分别约为500纳米和小于10纳米。作者测量了一氧化氮(NO)的产生作为炎症标志物,并使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)法检测线粒体活性,以此作为不同浓度水性SWCNT溶液处理后细胞层的细胞毒性反应。结果表明,暴露于不同浓度的碳纳米管后,NO的产生显著增加,细胞活力下降。测量跨共培养层的跨上皮电阻(TER),以观察暴露于不同浓度碳纳米管后气道生理功能的变化。暴露于20% SWCNT(8微克/毫升)后,TER值显著下降。在本研究中,作者提出了替代体内试验的可行方法,以评估工程化单壁碳纳米管的毒性。使用气道体外共培养系统观察了暴露于碳纳米管后人肺层的细胞毒性/炎症反应及屏障功能。