Purification and sidewall functionalization of multiwalled carbon nanotubes and resulting bioactivity in two macrophage models

  • Raymond F. Hamilton
  • , Chengcheng Xiang
  • , Ming Li
  • , Ibrahima Ka
  • , Feng Yang
  • , Dongling Ma
  • , Dale W. Porter
  • , Nianqiang Wu
  • , Andrij Holian

Research output: Contribution to journalArticlepeer-review

72 Scopus citations

Abstract

This study examined the consequences of surface carboxylation of multiwalled carbon nanotubes (MWCNT) on bioactivity. Since commercial raw MWCNT contain impurities that may affect their bioactivity, HCl refluxing was exploited to purify raw "as-received" MWCNT by removing the amorphous carbon layer on the MWCNT surface and reducing the metal impurities (e.g. Ni). The removal of amorphous carbon layer was confirmed by Raman spectroscopy and thermogravimetric analysis. Furthermore, the HCl-purified MWCNT provided more available reaction sites, leading to enhanced sidewall functionalization. The sidewall of HCl-purified MWCNT was further functionalized with the-COOH moiety by HNO3 oxidation. This process resulted in four distinct MWCNT: raw, purified,-COOH-terminated raw MWCNT, and-COOH-terminated purified MWCNT. Freshly isolated alveolar macrophages from C57Bl/6 mice were exposed to these nanomaterials to determine the effects of the surface chemistry on the bioactivity in terms of cell viability and inflammasome activation. Inflammasome activation was confirmed using inhibitors of cathepsin B and Caspase-1. Purification reduced the cell toxicity and inflammasome activation slightly compared to raw MWCNT. In contrast, functionalization of MWCNT with the-COOH group dramatically reduced the cytotoxicity and inflammasome activation. Similar results were seen using THP-1 cells supporting their potential use for high-throughput screening. This study demonstrated that the toxicity and bioactivity of MWCNT were diminished by removal of the Ni contamination and/or addition of-COOH groups to the sidewalls.

Original languageEnglish
Pages (from-to)199-210
Number of pages12
JournalInhalation Toxicology
Volume25
Issue number4
DOIs
StatePublished - Mar 2013

Funding

The authors report no conflicts of interest. The production, characterization, and toxicology studies were primarily supported by a NIH grant (1RC2ES018742). The authors acknowledge the following grants that contributed support: NIH R01 ES015497, NSF CBET-0834233, and COBRE P20 RR017670. The facilities and resources used in this work were partially supported by the NSF grant (EPS 0554328 and EPS 1003907) with matching funds from the West Virginia University Research Corporation and the West Virginia EPSCoR Office. The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the National Institute for Occupational Safety and Health.

FundersFunder number
EPS 0554328, EPS 1003907, P20 RR017670
CBET-0834233
R01 ES015497, 1RC2ES018742
P30GM103338
West Virginia State University

    Keywords

    • Carboxylated
    • Functionalized
    • Inflammasome
    • MWCNT
    • Toxicity

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