Toxicological Profiling of Highly Purified Single-Walled Carbon Nanotubes with Different Lengths in the Rodent Lung and Escherichia Coli

Small. 2018 Jun;14(23):e1703915. doi: 10.1002/smll.201703915. Epub 2018 May 7.

Abstract

Carbon nanotubes (CNTs) exhibit a number of physicochemical properties that contribute to adverse biological outcomes. However, it is difficult to define the independent contribution of individual properties without purified materials. A library of highly purified single-walled carbon nanotubes (SWCNTs) of different lengths is prepared from the same base material by density gradient ultracentrifugation, designated as short (318 nm), medium (789 nm), and long (1215 nm) SWCNTs. In vitro screening shows length-dependent interleukin-1β (IL-1β) production, in order of long > medium > short. However, there are no differences in transforming growth factor-β1 production in BEAS-2B cells. Oropharyngeal aspiration shows that all the SWCNTs induce profibrogenic effects in mouse lung at 21 d postexposure, but there are no differences between tube lengths. In contrast, these SWCNTs demonstrate length-dependent antibacterial effects on Escherichia coli, with the long SWCNT exerting stronger effects than the medium or short tubes. These effects are reduced by Pluronic F108 coating or supplementing with glucose. The data show length-dependent effects on proinflammatory response in macrophage cell line and antibacterial effects, but not on collagen deposition in the lung. These data demonstrate that over the length scale tested, the biological response to highly purified SWCNTs is dependent on the complexity of the nano/bio interface.

Keywords: antibacterial effects; density gradient ultracentrifugation (DGU); length sorting; lung fibrosis; single-walled carbon nanotubes (SWCNTs).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Cell Line
  • Cytokines / biosynthesis
  • Escherichia coli / drug effects*
  • Escherichia coli / growth & development
  • Escherichia coli / ultrastructure
  • Humans
  • Hydrodynamics
  • Inflammation / pathology
  • Inflammation Mediators / metabolism
  • Lung / drug effects*
  • Mice, Inbred C57BL
  • Nanotubes, Carbon / toxicity*
  • Nanotubes, Carbon / ultrastructure
  • Poloxamer / pharmacology
  • Static Electricity
  • Toxicity Tests*

Substances

  • Anti-Bacterial Agents
  • Cytokines
  • Inflammation Mediators
  • Nanotubes, Carbon
  • Poloxamer