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

<p>Abstract</p> <p>Background</p> <p>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...

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Main Authors: Mercer Robert R, Chen Bean, Mishra Anurag, Castranova Vincent, Wang Liying, Schwegler-Berry Diane, Rojanasakul Yon
Format: Article
Language:English
Published: BMC 2010-10-01
Series:Particle and Fibre Toxicology
Online Access:http://www.particleandfibretoxicology.com/content/7/1/31
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spelling doaj-615dba8ccba6440ba29a0d19f728b3af2020-11-24T22:12:44ZengBMCParticle and Fibre Toxicology1743-89772010-10-01713110.1186/1743-8977-7-31Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studiesMercer Robert RChen BeanMishra AnuragCastranova VincentWang LiyingSchwegler-Berry DianeRojanasakul Yon<p>Abstract</p> <p>Background</p> <p>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 <it>in vitro </it>and <it>in vivo</it>.</p> <p>Results</p> <p>The natural lung surfactant Survanta<sup>® </sup>was used to disperse single-walled carbon nanotubes (SWCNT) in a biological medium. At physiologically relevant concentrations, Survanta<sup>® </sup>produced well dispersed SWCNT without causing a cytotoxic or fibrogenic effect. <it>In vitro </it>studies show that Survanta<sup>®</sup>-dispersed SWCNT (SD-SWCNT) stimulated proliferation of lung epithelial cells at low doses (0.04-0.12 μg/ml or 0.02-0.06 μg/cm<sup>2 </sup>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 Survanta<sup>® </sup>did not mask the bioactivity of SWCNT. Likewise, <it>in vivo </it>studies show that both SD-SWCNT and AD-SWCNT induced lung fibrosis in mice, whereas the dispersing agent Survanta<sup>® </sup>alone or Survanta<sup>®</sup>-dispersed control ultrafine carbon black had no effect.</p> <p>Conclusions</p> <p>The results indicate that Survanta<sup>® </sup>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 <it>in vitro </it>and induced lung fibrosis <it>in vivo</it>. Similar results were observed with AD-SWCNT, supporting the conclusion that Survanta<sup>® </sup>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 <it>in vitro </it>model using lung fibroblasts may be an effective and rapid screening tool for prediction of the fibrogenic potential of SWCNT <it>in vivo</it>.</p> http://www.particleandfibretoxicology.com/content/7/1/31
collection DOAJ
language English
format Article
sources DOAJ
author Mercer Robert R
Chen Bean
Mishra Anurag
Castranova Vincent
Wang Liying
Schwegler-Berry Diane
Rojanasakul Yon
spellingShingle Mercer Robert R
Chen Bean
Mishra Anurag
Castranova Vincent
Wang Liying
Schwegler-Berry Diane
Rojanasakul Yon
Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
Particle and Fibre Toxicology
author_facet Mercer Robert R
Chen Bean
Mishra Anurag
Castranova Vincent
Wang Liying
Schwegler-Berry Diane
Rojanasakul Yon
author_sort Mercer Robert R
title Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
title_short Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
title_full Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
title_fullStr Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
title_full_unstemmed Dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
title_sort dispersion of single-walled carbon nanotubes by a natural lung surfactant for pulmonary <it>in vitro </it>and <it>in vivo </it>toxicity studies
publisher BMC
series Particle and Fibre Toxicology
issn 1743-8977
publishDate 2010-10-01
description <p>Abstract</p> <p>Background</p> <p>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 <it>in vitro </it>and <it>in vivo</it>.</p> <p>Results</p> <p>The natural lung surfactant Survanta<sup>® </sup>was used to disperse single-walled carbon nanotubes (SWCNT) in a biological medium. At physiologically relevant concentrations, Survanta<sup>® </sup>produced well dispersed SWCNT without causing a cytotoxic or fibrogenic effect. <it>In vitro </it>studies show that Survanta<sup>®</sup>-dispersed SWCNT (SD-SWCNT) stimulated proliferation of lung epithelial cells at low doses (0.04-0.12 μg/ml or 0.02-0.06 μg/cm<sup>2 </sup>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 Survanta<sup>® </sup>did not mask the bioactivity of SWCNT. Likewise, <it>in vivo </it>studies show that both SD-SWCNT and AD-SWCNT induced lung fibrosis in mice, whereas the dispersing agent Survanta<sup>® </sup>alone or Survanta<sup>®</sup>-dispersed control ultrafine carbon black had no effect.</p> <p>Conclusions</p> <p>The results indicate that Survanta<sup>® </sup>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 <it>in vitro </it>and induced lung fibrosis <it>in vivo</it>. Similar results were observed with AD-SWCNT, supporting the conclusion that Survanta<sup>® </sup>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 <it>in vitro </it>model using lung fibroblasts may be an effective and rapid screening tool for prediction of the fibrogenic potential of SWCNT <it>in vivo</it>.</p>
url http://www.particleandfibretoxicology.com/content/7/1/31
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