Functionalization has been shown to alter toxicity of multi-walled carbon nanotube (MWCNT) in several studies. This study varied the degree of functionalization (viz.， amount of MWCNT surface carboxylation) to define the relationship between the extent of carboxylation and effects in a variety of in vitro cell models and short-term ex vivo/in vivo particle exposures. Studies with vitamin D₃ plus phorbol ester transformed THP-1 macrophages demonstrated that functionalization， regardless of amount， corresponded with profoundly decreased NLRP3 inflammasome activation. However， all MWCNT variants were slightly toxic in this model. Alternatively， studies with A549 epithelial cells showed some varied effe... More
Functionalization has been shown to alter toxicity of multi-walled carbon nanotube (MWCNT) in several studies. This study varied the degree of functionalization (viz.， amount of MWCNT surface carboxylation) to define the relationship between the extent of carboxylation and effects in a variety of in vitro cell models and short-term ex vivo/in vivo particle exposures. Studies with vitamin D₃ plus phorbol ester transformed THP-1 macrophages demonstrated that functionalization， regardless of amount， corresponded with profoundly decreased NLRP3 inflammasome activation. However， all MWCNT variants were slightly toxic in this model. Alternatively， studies with A549 epithelial cells showed some varied effects. For example， IL-33 and TNF-α release were related to varying amounts of functionalization. For in vivo particle exposures， autophagy of alveolar macrophages， measured using green fluorescent protein (GFP)- fused-LC3 transgenic mice， increased for all MWCNT tested three days after exposure， but， by Day 7， autophagy was clearly dependent on the amount of carboxylation. The instilled source MWCNT continued to produce cellular injury in alveolar macrophages over seven days. In contrast， the more functionalized MWCNT initially showed similar effects， but reduced over time. Dark-field imaging showed the more functionalized MWCNTs were distributed more uniformly throughout the lung and not isolated to macrophages. Taken together， the results indicated that in vitro and in vivo bioactivity of MWCNT decreased with increased carboxylation. Functionalization by carboxylation eliminated the bioactive potential of the MWCNT in the exposure models tested. The observation that maximally functionalized MWCNT distribute more freely throughout the lung with the absence of cellular damage， and extended deposition， may establish a practical use for these particles as a safer alternative for unmodified MWCNT.
