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contributor authorGernand, Jeremy M.
contributor authorCasman, Elizabeth A.
date accessioned2017-05-09T01:25:28Z
date available2017-05-09T01:25:28Z
date issued2016
identifier issn2332-9017
identifier otherRISK_2_2_021002.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/160168
description abstractDue to their unique physicochemical properties, nanomaterials have the potential to interact with living organisms in novel ways. Nanomaterial variants are too numerous to be screened for toxicity individually by traditional animal testing. Existing data on the toxicity of inhaled nanomaterials in animal models are sparse in comparison to the number of potential factors that may affect toxicity. This paper presents metaanalysisbased risk models developed with the machinelearning technique, random forests (RFs), to determine the relative contribution of different physical and chemical attributes on observed toxicity. The findings from this analysis indicate that carbon nanotube (CNT) impurities explain at most 30% of the variance in pulmonary toxicity as measured by polymorphonuclear neutrophils (PMNs) count. Titanium dioxide nanoparticle size and aggregation affected the observed toxic response by less than 10%. Differences in observed effects for a group of metal oxide nanoparticles associated with differences in Gibbs free energy on lactate dehydrogenase (LDH) concentrations amount to only 4% to the total variance.
publisherThe American Society of Mechanical Engineers (ASME)
titleNanoparticle Characteristic Interaction Effects on Pulmonary Toxicity: A Random Forest Modeling Framework to Compare Risks of Nanomaterial Variants
typeJournal Paper
journal volume2
journal issue2
journal titleASCE-ASME Journal of Risk and Uncertainty in Engineering Systems, Part B: Mechanical Engineering
identifier doi10.1115/1.4031216
journal fristpage21002
journal lastpage1
treeASCE-ASME Journal of Risk and Uncertainty in Engineering Systems, Part B: Mechanical Engineering:;2016:;volume( 002 ):;issue: 002
contenttypeFulltext


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