Pluronic F108 Coating Decreases the Lung Fibrosis Potential of Multiwall Carbon Nanotubes by Reducing Lysosomal Injury

We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability as well as profibrogenic effects in vitro and in vivo. While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating...

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Published inNano letters Vol. 12; no. 6; pp. 3050 - 3061
Main Authors Wang, Xiang, Xia, Tian, Duch, Matthew C, Ji, Zhaoxia, Zhang, Haiyuan, Li, Ruibin, Sun, Bingbing, Lin, Sijie, Meng, Huan, Liao, Yu-Pei, Wang, Meiying, Song, Tze-Bin, Yang, Yang, Hersam, Mark C, Nel, André E
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 13.06.2012
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Abstract We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability as well as profibrogenic effects in vitro and in vivo. While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating protected the tubes from damaging the lysosomal membrane and initiating a sequence of cooperative cellular events that play a role in the pathogenesis of pulmonary fibrosis. Our results suggest that PF108 coating could serve as a safer design approach for MWCNTs.
AbstractList We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability as well as profibrogenic effects in vitro and in vivo. While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating protected the tubes from damaging the lysosomal membrane and initiating a sequence of cooperative cellular events that play a role in the pathogenesis of pulmonary fibrosis. Our results suggest that PF108 coating could serve as a safer design approach for MWCNTs.
We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability as well as profibrogenic effects in vitro and in vivo. While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating protected the tubes from damaging the lysosomal membrane and initiating a sequence of cooperative cellular events that play a role in the pathogenesis of pulmonary fibrosis. Our results suggest that PF108 coating could serve as a safer design approach for MWCNTs.We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability as well as profibrogenic effects in vitro and in vivo. While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating protected the tubes from damaging the lysosomal membrane and initiating a sequence of cooperative cellular events that play a role in the pathogenesis of pulmonary fibrosis. Our results suggest that PF108 coating could serve as a safer design approach for MWCNTs.
We compared the use of bovine serum albumin (BSA) and Pluronic F108 (PF108) as dispersants for multi-walled carbon nanotubes (MWCNTs) in terms of tube stability as well as pro-fibrogenic effects in vitro and in vivo . While BSA-dispersed tubes were a potent inducer of pulmonary fibrosis, PF108 coating protected the tubes from damaging the lysosomal membrane and initiating a sequence of cooperative cellular events that play a role in the pathogenesis of pulmonary fibrosis. Our results suggest that PF108 coating could be served as a safer design approach for MWCNTs.
Author Hersam, Mark C
Sun, Bingbing
Liao, Yu-Pei
Wang, Meiying
Meng, Huan
Song, Tze-Bin
Nel, André E
Yang, Yang
Wang, Xiang
Duch, Matthew C
Ji, Zhaoxia
Xia, Tian
Li, Ruibin
Lin, Sijie
Zhang, Haiyuan
AuthorAffiliation Northwestern University
University of California
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– name: Northwestern University
– name: Division of NanoMedicine, Department of Medicine, Northwestern University, Evanston, Illinois 60208, United States
– name: Department of Materials Science and Engineering, University of California, Los Angeles, CA 90095, United States
– name: ζ Departments of Materials Science and Engineering, Chemistry, and Medicine, Northwestern University, Evanston, Illinois 60208, United States
– name: California NanoSystems Institute, Northwestern University, Evanston, Illinois 60208, United States
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  givenname: Tian
  surname: Xia
  fullname: Xia, Tian
– sequence: 3
  givenname: Matthew C
  surname: Duch
  fullname: Duch, Matthew C
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  givenname: Zhaoxia
  surname: Ji
  fullname: Ji, Zhaoxia
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  surname: Wang
  fullname: Wang, Meiying
– sequence: 12
  givenname: Tze-Bin
  surname: Song
  fullname: Song, Tze-Bin
– sequence: 13
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– sequence: 14
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  surname: Hersam
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  givenname: André E
  surname: Nel
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  email: anel@mednet.ucla.edu
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Keywords biocompatible
pluronic copolymer
dispersion
lung fibrosis
Multiwalled carbon nanotubes (MWCNTs)
In vivo
Multiwalled nanotube
Carbon nanotubes
Serum albumin
Damage
Coatings
Nanostructured materials
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Snippet We compared the use of bovine serum albumin (BSA) and pluronic F108 (PF108) as dispersants for multiwalled carbon nanotubes (MWCNTs) in terms of tube stability...
We compared the use of bovine serum albumin (BSA) and Pluronic F108 (PF108) as dispersants for multi-walled carbon nanotubes (MWCNTs) in terms of tube...
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SubjectTerms Administration, Inhalation
Animals
Cellular
Coated Materials, Biocompatible - chemistry
Coating
Cross-disciplinary physics: materials science; rheology
Exact sciences and technology
Fibrosis
Injury prevention
Lysosomes - drug effects
Lysosomes - pathology
Materials science
Mice
Multi wall carbon nanotubes
Nanocrystalline materials
Nanoscale materials and structures: fabrication and characterization
Nanostructure
Nanotubes
Nanotubes, Carbon - toxicity
Physics
Poloxamer - chemistry
Pulmonary Fibrosis - chemically induced
Pulmonary Fibrosis - pathology
Pulmonary Fibrosis - prevention & control
Serum albumin
Surgical implants
Tubes
Title Pluronic F108 Coating Decreases the Lung Fibrosis Potential of Multiwall Carbon Nanotubes by Reducing Lysosomal Injury
URI http://dx.doi.org/10.1021/nl300895y
https://www.ncbi.nlm.nih.gov/pubmed/22546002
https://www.proquest.com/docview/1020509638
https://www.proquest.com/docview/1762050599
https://pubmed.ncbi.nlm.nih.gov/PMC4143198
Volume 12
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