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Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary in vitro and in vivo toxicity studies.

Authors
Wang-L; Castranova-V; Mishra-A; Chen-B; Mercer-RR; Schwegler-Berry-D; Rojanasakul-Y
Source
Part Fibre Toxicol 2010 Oct; 7:31
NIOSHTIC No.
20037852
Abstract
Background: Accumulating evidence indicate that the degree of dispersion of nanoparticles has a strong influence on their biological activities. The aims of this study were to develop a simple and rapid method of nanoparticle dispersion using a natural lung surfactant and to evaluate the effect of dispersion status of SWCNT on cytotoxicity and fibrogenicity in vitro and in vivo. Results: The natural lung surfactant SurvantaŽ was used to disperse single-walled carbon nanotubes (SWCNT) in a biological medium. At physiologically relevant concentrations, SurvantaŽ produced well dispersed SWCNT without causing a cytotoxic or fibrogenic effect. In vitro studies show that SurvantaŽ-dispersed SWCNT (SD-SWCNT) stimulated proliferation of lung epithelial cells at low doses (0.04-0.12 ug/ml or 0.02-0.06 ug/cm2 exposed surface area) but had a suppressive effect at high doses. Non-dispersed SWCNT (ND-SWCNT) did not exhibit these effects, suggesting the importance of dispersion status of SWCNT on bioactivities. Studies using cultured human lung fibroblasts show that SD-SWCNT stimulated collagen production of the cells. This result is supported by a similar observation using Acetone/sonication dispersed SWCNT (AD-SWCNT), suggesting that SurvantaŽ did not mask the bioactivity of SWCNT. Likewise, in vivo studies show that both SD-SWCNT and AD-SWCNT induced lung fibrosis in mice, whereas the dispersing agent SurvantaŽ alone or SurvantaŽ-dispersed control ultrafine carbon black had no effect. Conclusions: The results indicate that SurvantaŽ was effective in dispersing SWCNT in biological media without causing cytotoxic effects at the test concentrations used in this study. SD-SWCNT stimulated collagen production of lung fibroblasts in vitro and induced lung fibrosis in vivo. Similar results were observed with AD-SWCNT, supporting the conclusion that SurvantaŽ did not mask the bioactivities of SWCNT and thus can be used as an effective dispersing agent. Since excessive collagen production is a hallmark of lung fibrosis, the results of this study suggest that the in vitro model using lung fibroblasts may be an effective and rapid screening tool for prediction of the fibrogenic potential of SWCNT in vivo.
Keywords
Biological-effects; Biological-factors; Biological-monitoring; Biological-systems; Biological-transport; Cell-biology; Cytotoxic-effects; Dose-response; Exposure-assessment; Exposure-levels; Exposure-methods; Fibrogenesis; Fibrous-bodies; Injury-prevention; Laboratory-animals; Laboratory-testing; Lung-cells; Mathematical-models; Nanotechnology; Physiological-effects; Physiological-factors; Physiological-measurements; Physiological-response; Quantitative-analysis; Statistical-analysis
Contact
Liying Wang, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, 1095 Willowdale Road M/S 4050, Morgantown, WV 26505
Publication Date
20101019
Document Type
Journal Article
Email Address
lmw6@cdc.gov
Fiscal Year
2011
NTIS Accession No.
NTIS Price
ISSN
1743-8977
NIOSH Division
HELD
Priority Area
Manufacturing
Source Name
Particle and Fibre Toxicology
State
WV
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