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• SWMC-O031<br />

OXYGEN CONTENT DETERMINES THE BIO-REACTIVITY AND<br />

TOXICITY PROFILES OF CARBON BLACK PARTICLES<br />

Sijin Liu 1<br />

1 Research Center for Eco-Environmental Sciences, State Key Laboratory of Environment<br />

Chemistry and Ecotoxicology, China.<br />

In spite of the considerable efforts invested to understand the environmental<br />

health and safety (EHS) impacts of ultrafine particles, such as the representative<br />

PM2.5, there are still significant knowledge gaps to be filled. No conclusive<br />

understandings have been obtained about the physicochemical determinants in<br />

accounting for differential adverse outcomes. Here we compared the<br />

cytotoxicity of four carbon black (CB) particles with similar physicochemical<br />

properties except for their oxygen contents (C824455 < C1864 < Printex U <<br />

SB4A). We found that these four CB particles manifested in vitro and in vivo<br />

cytotoxicity reversely related to their oxygen contents, namely a hierarchy of<br />

cytotoxicity: C824455 > C1864 > Printex U > SB4A. Among these CB particles, the<br />

most significant lung injury (e.g. collapses and inflammation) and macrophagic<br />

activation were found for C824455 and C1864, in particular for C824455. All<br />

these differences in toxicity profiles, including in vitro and in vivo cytotoxicity,<br />

pro-inflammatory effects and direct damages to the lung epithelia, should be (at<br />

least partially) ascribed to the oxygen content in these CB particles that in turn<br />

determined their transformation, i.e. the different aggregation states.<br />

Nonetheless, PM2.5 likewise caused severe in vivo and in vitro toxicities to the<br />

lung cells and macrophages. This study thus offers more insights into the<br />

structure-activity relationship (SAR) and opens a new avenue to elucidate the<br />

physicochemical determinants in evoking lung injuries by ultrafine airborne<br />

particles.<br />

Acknowledgment: This work was supported by grants the National Natural<br />

Science Foundation of China (Grant nos.: 21425731, 21637004 and 91543124),<br />

a grant under the national “973” Program (Grant no.: 2014CB932000), and the<br />

Strategic Priority Research Program of the Chinese Academy of Sciences (Grant<br />

no. XDB14000000).<br />

Keywords: Carbon black, Inflammatory responses, Macrophage<br />

Presenting authors email: sjliu@rcees.ac.cn

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