Abstract
The elucidation of toxicity determinants of multi-walled carbon nanotubes (MWCNT) is still incomplete. Functionalization with carboxyl groups is, however, commonly used to mitigate MWCNT toxicity, although the rationale for the mitigating effect has not been fully clarified yet. In this work, two optimized chemical vapor deposition methods were employed to obtain MWCNT of comparable length but different diameter, which were subsequently functionalized. For MWCNT of diameter larger than 40nm, no detrimental effects on cell viability of macrophages were observed, while mild cytotoxicity was recorded for diameters between 15 and 40nm, with a mitigating effect of functionalization. To investigate the factors responsible for the mitigation, we used the thinnest MWCNT preparation on different cell models, evaluating several endpoints, such as viability, production of nitric oxide (NO), expression of pro-inflammatory markers, the Trans-Epithelial Electrical Resistance (TEER), and clonogenic activity. Substantial mitigation of the changes caused by pristine MWCNT was observed not only with carboxyl- but also with amino-functionalized MWCNT, suggesting that negative or positive surface charge was not the main factor responsible for the effect. Instead, either functionalized preparation exhibited a stronger tendency to agglomerate that was strictly dependent on the presence of proteins. Moreover, we found that either carboxyl- or amino-functionalized MWCNT adsorbed a larger amount of serum proteins than pristine counterparts, with a distinctive pattern for each type of MWCNT. We propose, therefore, that the formation of larger agglomerates, dependent upon different protein coronae, contributes to mitigate the biological effects of functionalized MWCNT in protein-rich biological media.
Highlights
Various factors influence the biological effects of multi-walled carbon nanotubes (MWCNT) and have the potential to modulate their biological effects [28]
A correlation has been reported between MWCNT toxicity, their size [28,34], contamination with metal catalysts [1], and surface functionalization [28]
It is difficult to find examples in literature where differences between two MWCNT preparations are limited to one parameter, allowing a clear cut assessment of its contribution to the toxicological properties of the nanomaterial
Summary
A specific MWCNT preparation (MWCNT-7) has been recently classified as possibly carcinogenic to humans (Group 2B) by the International Agency for Research on Cancer, other preparations of MWCNT were not classifiable respect to their carcinogenicity to humans [26] These contrasting results can be attributed to the use of materials with different degree of purity and structural features [68], as well as to the conditions adopted for the in vitro studies [72] and the cell types tested for the assays [35]. We tested the hypothesis that functionalization with carboxyl or amino groups affects the formation of protein corona and, the biological effects of MWCNT To this purpose, we preliminary examined four MWCNT preparations, three synthesized in our laboratory via CVD method and one commercial, of comparable length but different diameter and surface chemistry, and compared their effects on cell viability with those exhibited by a benchmark MWCNT preparation obtained from the Joint Research. One of the preparations exhibiting changes in biological activity attributable to functionalization was further investigated, studying both protein corona and several toxicological endpoints
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