2016
DOI: 10.2147/ijn.s123839
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<div>Long-term intravenous administration of carboxylated single-walled carbon nanotubes induces persistent accumulation in the lungs and pulmonary fibrosis via the nuclear factor-kappa B pathway</div>

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Cited by 34 publications
(10 citation statements)
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“…Some studies demonstrated that CNTs, even in low concentrations, are able to trigger inflammation in the respiratory system of animals [168]. In addition to inflammation, it was revealed that CNTs are also capable of inducing the modulation of proliferation of lung cells as a result of direct injury [169], fibrosis [170], DNA damage [171], and lung cancer [172,173].…”
Section: Toxicity Studies Of Carbon Nanotubesmentioning
confidence: 99%
“…Some studies demonstrated that CNTs, even in low concentrations, are able to trigger inflammation in the respiratory system of animals [168]. In addition to inflammation, it was revealed that CNTs are also capable of inducing the modulation of proliferation of lung cells as a result of direct injury [169], fibrosis [170], DNA damage [171], and lung cancer [172,173].…”
Section: Toxicity Studies Of Carbon Nanotubesmentioning
confidence: 99%
“…Indeed, CNTs induce adverse effects, particularly on the respiratory tract, which constitutes the main route for penetration of these nanomaterials. They cause inflammatory, immunologic and fibrogenic effects in rodent lungs (Duke et al, 2017;Qin et al, 2017). Furthermore, key events shown on a cellular level, with NR8383 cells reveal that CNTs play a vital role in cell growth inhibition, production of reactive oxygen species (Fujita et al, 2015) and decrease of the mitochondrial membrane potential (Pulskamp, Diabaté, & Krug, 2007).…”
mentioning
confidence: 99%
“…In spite of their beneficial role in various diseases, a study reported that the repeated and long-term administration of carboxylated SWNTsintravenously results in the persistent accumulation in the lungs, can cause the embolization of lung capillaries, the formation of granuloma, and can induce the NF–kappaB pathway that leads to pulmonary fibrosis. Additionally, pro-fibrotic growth factors (transforming growth factor-beta 1), pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-1 beta), fibrotic markers(type-III collagens, matrix metalloproteinase-2, type-I collagen and metalloproteinase-2), and a tissue inhibitor were reported as having high post-exposure expressions after the intravenous administration of c-SWNTs, suggesting that cumulative and chronic toxicity to organs because of nanomaterials should be analyzed while administering intravenously [ 64 ]. In a study, it was reported that carboxyl group-functionalized multi-walled carbon nanotubes effectively enhanced the differentiation and mineralization of mammalian cementoblaststhrough interactions with the TGF-β/Smad pathway [ 65 ].…”
Section: Types Of Nanoparticlesmentioning
confidence: 99%