Literature DB >> 22724895

Does carbon black disaggregate in lung fluid? A critical assessment.

Len Levy1, Ishrat S Chaudhuri, Nils Krueger, Robert J McCunney.   

Abstract

Carbon black is an industrially produced particulate form of nearly pure elemental carbon. The basic building blocks of carbon black are (1) primary particles, minute pieces of matter with defined physical boundaries; (2) aggregates, collections of strongly bound or fused particles; and (3) agglomerates, collections of weakly bound aggregates. Industrial carbon black is produced within a closed reactor where the primary particles form aggregates, which become the indivisible entities of carbon black. These aggregates then form agglomerates, which are the typical form of carbon black in commerce. Carbon black is often used in in vitro and in vivo particle toxicology investigations as a reference nanoparticle. The toxicology studies often report the sizes of the primary particles but rarely the sizes of the aggregates or agglomerates. It appears in many cases that there is a limited understanding of the fact that carbon black typically does not exist as primary particles but instead exists as aggregates and agglomerates. Moreover, many toxicology studies manipulate carbon black particles in order to disperse them so that the form of carbon black used in these toxicology studies may be substantially different from the form that may be encountered in the workplace environment. Since the main exposure route for carbon black is inhalation, the question arose as to whether inhaled carbon black may deagglomerate or disaggregate to either smaller aggregates or primary particles when in contact with lung fluids. This question relates to the concern that there may be additional hazards of smaller particles, such as their ability to translocate to tissues and organs beyond the lung and the ability to pass through the blood-brain barrier. The purpose of this assessment is to review the existing literature for evidence as to whether carbon black deagglomerates or disaggregates into smaller aggregates or primary particles when in contact with lung fluid. On the basis of a review of the physical characteristics of commercial carbon black and various toxicology studies, it appears that commercially produced carbon black in contact with lung fluid is unlikely to deagglomerate or disaggregate into smaller aggregates or primary particles.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22724895     DOI: 10.1021/tx300160z

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  5 in total

1.  Biokinetics of Nanomaterials: the Role of Biopersistence.

Authors:  Peter Laux; Christian Riebeling; Andy M Booth; Joseph D Brain; Josephine Brunner; Cristina Cerrillo; Otto Creutzenberg; Irina Estrela-Lopis; Thomas Gebel; Gunnar Johanson; Harald Jungnickel; Heiko Kock; Jutta Tentschert; Ahmed Tlili; Andreas Schäffer; Adriënne J A M Sips; Robert A Yokel; Andreas Luch
Journal:  NanoImpact       Date:  2017-03-22

2.  Intratracheally instilled titanium dioxide nanoparticles translocate to heart and liver and activate complement cascade in the heart of C57BL/6 mice.

Authors:  Mainul Husain; Dongmei Wu; Anne T Saber; Nathalie Decan; Nicklas R Jacobsen; Andrew Williams; Carole L Yauk; Hakan Wallin; Ulla Vogel; Sabina Halappanavar
Journal:  Nanotoxicology       Date:  2015-05-20       Impact factor: 5.913

3.  Cohort Study of Carbon Black Exposure and Risk of Malignant and Nonmalignant Respiratory Disease Mortality in the US Carbon Black Industry.

Authors:  Linda D Dell; Alexa E Gallagher; Lori Crawford; Rachael M Jones; Kenneth A Mundt
Journal:  J Occup Environ Med       Date:  2015-09       Impact factor: 2.162

4.  Size-dependent cytotoxicity of nanocarbon blacks.

Authors:  Huating Kong; Yu Zhang; Yongjun Li; Zhifen Cui; Kai Xia; Yanhong Sun; Qunfen Zhao; Ying Zhu
Journal:  Int J Mol Sci       Date:  2013-11-14       Impact factor: 5.923

5.  Carbon black nanoparticles induce biphasic gene expression changes associated with inflammatory responses in the lungs of C57BL/6 mice following a single intratracheal instillation.

Authors:  Mainul Husain; Zdenka O Kyjovska; Julie Bourdon-Lacombe; Anne T Saber; Keld A Jensen; Nicklas R Jacobsen; Andrew Williams; Håkan Wallin; Sabina Halappanavar; Ulla Vogel; Carole L Yauk
Journal:  Toxicol Appl Pharmacol       Date:  2015-11-10       Impact factor: 4.219

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.