Impaired Clearance And Enhanced Pulmonary Inflammatory/Fibrotic Response To Carbon Nanotubes In Myeloperoxidase-Deficient Mice

Abstract

Advancement of biomedical applications of carbonaceous nanomaterials is hampered by their biopersistence and proinflammatory action in vivo. Here, we used myeloperoxidase knockout B6.129X1-MPO (MPO k/o) mice and showed that oxidation and clearance of single walled carbon nanotubes (SWCNT) from the lungs of these animals after pharyngeal aspiration was markedly less effective whereas the inflammatory response was more robust than in wild-type C57Bl/6 mice. Our results provide direct evidence for the participation of MPO - one of the key-orchestrators of inflammatory response - in the in vivo pulmonary oxidative biodegradation of SWCNT and suggest new ways to control the biopersistence of nanomaterials through genetic or pharmacological manipulations.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Mar 30, 2012
Accession Number
ADA559018

Entities

People

  • Anna A. Shvedova
  • Ashley R. Murray
  • Claudette M. St. Croix
  • Elena R. Kisin
  • Megan A. Lang
  • Nagarjun V. Konduru
  • Oleksandr Kapralov
  • Robert R. Mercer
  • Simon C Watkins
  • Wei H. Feng

Organizations

  • University of Pittsburgh

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Biodegradation
  • Carbon Nanotubes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Connective Tissue
  • Environmental Health
  • Fullerenes
  • Materials
  • Measurement
  • Microscopes
  • Nanomaterials
  • Nanotechnology
  • Raman Spectra
  • Raman Spectroscopy
  • Stem Cells
  • United States

Readers

  • Immunology and Pathology
  • Nanocomposite Materials Science

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech