Literature DB >> 21654426

Carbon nanotube risk assessment: implications for exposure and medical monitoring.

Eileen D Kuempel1.   

Abstract

OBJECTIVE: Quantitative risk estimates using toxicology data provide information for risk management to protect workers with potential exposure to carbon nanotubes (CNTs).
METHODS: Dose-response data from subchronic inhalation studies in rats were used in benchmark dose modeling. Dose was airborne mass concentration of multiwalled CNTs. Responses included pulmonary inflammation, lipoproteinosis, and fibrosis.
RESULTS: Estimated human-equivalent concentrations to the rat lowest observed adverse effect levels were similar to some workplace airborne concentrations of CNTs. Working lifetime risk estimates of early-stage adverse lung effects were more than 10% at the limit of quantification (7 μg/m³) of the National Institute for Occupational Safety and Health analytical method for measuring CNT airborne concentrations.
CONCLUSIONS: Exposure monitoring and control are the primary occupational health measures to protect workers from potential exposure to CNT. Medical monitoring for early detection of occupational respiratory diseases may also be warranted.

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Year:  2011        PMID: 21654426     DOI: 10.1097/JOM.0b013e31821b1f3f

Source DB:  PubMed          Journal:  J Occup Environ Med        ISSN: 1076-2752            Impact factor:   2.162


  4 in total

1.  Perspectives on the design of safer nanomaterials and manufacturing processes.

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Review 2.  Perturbation of pulmonary immune functions by carbon nanotubes and susceptibility to microbial infection.

Authors:  Brent E Walling; Gee W Lau
Journal:  J Microbiol       Date:  2014-03-01       Impact factor: 3.422

3.  Lung carcinogenicity of inhaled multi-walled carbon nanotube in rats.

Authors:  Tatsuya Kasai; Yumi Umeda; Makoto Ohnishi; Takashi Mine; Hitomi Kondo; Tetsuya Takeuchi; Michiharu Matsumoto; Shoji Fukushima
Journal:  Part Fibre Toxicol       Date:  2016-10-13       Impact factor: 9.400

4.  Helical carbon nanotubes enhance the early immune response and inhibit macrophage-mediated phagocytosis of Pseudomonas aeruginosa.

Authors:  Brent E Walling; Zhizhou Kuang; Yonghua Hao; David Estrada; Joshua D Wood; Feifei Lian; Lou Ann Miller; Amish B Shah; Jayme L Jeffries; Richard T Haasch; Joseph W Lyding; Eric Pop; Gee W Lau
Journal:  PLoS One       Date:  2013-11-18       Impact factor: 3.240

  4 in total

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