Comparative Toxicity of Nanomaterials to Air-blood Barrier Permeability Using an In Vitro Model

To comparatively study the toxicity of four metal-containing nanoparticles (MNPs) and their chemical counterparts to the air-blood barrier (ABB) permeability using an in vitro model. ABB model, which was developed via the co-culturing of A549 and pulmonary capillary endothelium, was exposed to spher...

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Veröffentlicht in:Biomedical and environmental sciences 2019-08, Vol.32 (8), p.602-613
Hauptverfasser: ZHAO, Kang Feng, SONG, Yu Qing, ZHANG, Rui Hua, YANG, Xiao Yan, SUN, Bo, HOU, Zhi Quan, PU, Xiao Ping, DAI, Hong Xing, BAI, Xue Tao
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Sprache:eng
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Zusammenfassung:To comparatively study the toxicity of four metal-containing nanoparticles (MNPs) and their chemical counterparts to the air-blood barrier (ABB) permeability using an in vitro model. ABB model, which was developed via the co-culturing of A549 and pulmonary capillary endothelium, was exposed to spherical CuO-NPs (divided into CuO-40, CuO-80, and CuO-100 based on particle size), nano-Al2O3 (sheet and short-rod-shaped), nano-ZnO, nano-PbS, CuSO4, Al2(SO4)3, Zn(CH3COO)2, and Pb(NO3)2 for 60 min. Every 10 min following exposure, the cumulative cleared volume (ΔTCL) of Lucifer yellow by the model was calculated. A clearance curve was established using linear regression analysis of ΔTCL versus time. Permeability coefficient (P) was calculated based on the slope of the curve to represent the degree of change in the ABB permeability. The results found the increased P values of CuO-40, CuO-80, sheet, and short-rod-shaped nano-Al2O3, Al2(SO4)3, and Pb(NO3)2. Among them, small CuO-40 and CuO-80 were stronger than CuO-100 and CuSO4; no difference was observed between Al2(SO4)3 and sheet and short-rod-shaped nano-Al2O3; and nano-PbS was slightly weaker than Pb(NO3)2. So clearly the MNPs possess diverse toxicity. ABB permeability abnormality means pulmonary toxicity potential. More studies are warranted to understand MNPs toxicity and ultimately control the health hazards.
ISSN:0895-3988
2214-0190
DOI:10.3967/bes2019.078