Evidence map›Paper›PMID 27459049›Full record

ArticleACS nano2016

Multiwalled Carbon Nanotube Functionalization with High Molecular Weight Hyaluronan Significantly Reduces Pulmonary Injury.

Salik Hussain, Zhaoxia Ji, Alexia J Taylor, Laura M DeGraff, Margaret George, Charles J Tucker, Chong Hyun Chang, Ruibin Li, James C Bonner, Stavros Garantziotis

Abstract read
In one paragraph

Article in ACS nano, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 54 citations in OpenAlex.

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  10. Drug delivery carriers with therapeutic functions.Advanced drug delivery reviews · 2021
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  19. Mechanisms of carbon nanotube-induced pulmonary fibrosis: a physicochemical characteristic perspective.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2018
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Salik HussainClinical Research Unit, National Institute of Environmental Health Sciences (NIEHS)/National Institute of Health (NIH) , Research Triangle Park, North Carolina 27709, United States.
Zhaoxia JiUC Center for Environmental Implications of Nanotechnology, University of California , Los Angeles, California 90095, United States.
Alexia J TaylorToxicology Program, Department of Biological Sciences, North Carolina State University , Raleigh, North Carolina 27695, United States.
Laura M DeGraff
Margaret GeorgeClinical Research Unit, National Institute of Environmental Health Sciences (NIEHS)/National Institute of Health (NIH) , Research Triangle Park, North Carolina 27709, United States.
Charles J Tucker
Chong Hyun ChangUC Center for Environmental Implications of Nanotechnology, University of California , Los Angeles, California 90095, United States.
Ruibin LiUC Center for Environmental Implications of Nanotechnology, University of California , Los Angeles, California 90095, United States.
James C BonnerToxicology Program, Department of Biological Sciences, North Carolina State University , Raleigh, North Carolina 27695, United States.
Stavros GarantziotisClinical Research Unit, National Institute of Environmental Health Sciences (NIEHS)/National Institute of Health (NIH) , Research Triangle Park, North Carolina 27709, United States.
National Institute of Environmental Health Sciences · USNorth Carolina State University · USUniversity of California, Los Angeles · USSoochow University · CN

Funding

Program in Clinical Research, Clinical Support Services and Clinical TrainingZIDES102465 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KIRSCHNER, LAWRENCE · 2009 to 2025
$84.7M
The Role of Hyaluronan And Inter-Alpha-Trypsin Inhibitor in Tissue InjuryZIAES102605 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI GARANTZIOTIS, STAVROS · 2009 to 2025
$22.6M
Scientific Core: Acquisition, Synthesis, and Characterization of NanomaterialsU19ES019528 · NIEHS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI XIA, TIAN · 2010 to 2014
$5.5M
Predictive Toxicological Paradigm for Chronic Nanoparticle Injury in the LungR01ES016746 · NIEHS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NEL, ANDRE ELIAS · 2008 to 2017
$3.4M
Genetic Susceptibility to Nanoparticle-Induced Respiratory DiseaseR01ES020897 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI BONNER, JAMES CHRISTOPHER · 2012 to 2017
$1.7M
The Role of Hyaluronan And Inter-Alpha-Trypsin Inhibitor in Tissue InjuryZ01ES102605 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI GARANTZIOTIS, STAVROS · 2008 to 2008
$621k
Intramural NIH HHS Z01 ES102605Intramural NIH HHS ZIA ES102605NIEHS NIH HHS R01 ES016746NIEHS NIH HHS R01 ES020897NIEHS NIH HHS U19 ES019528
6 · The paper itself

Abstract

Commercialization of multiwalled carbon nanotubes (MWCNT)-based applications has been hampered by concerns regarding their lung toxicity potential. Hyaluronic acid (HA) is a ubiquitously found polysaccharide, which is anti-inflammatory in its native high molecular weight form. HA-functionalized smart MWCNTs have shown promise as tumor-targeting drug delivery agents and can enhance bone repair and regeneration. However, it is unclear whether HA functionalization could reduce the pulmonary toxicity potential of MWCNTs. Using in vivo and in vitro approaches, we investigated the effectiveness of MWCNT functionalization with HA in increasing nanotube biocompatibility and reducing lung inflammatory and fibrotic effects. We utilized three-dimensional cultures of differentiated primary human bronchial epithelia to translate findings from rodent assays to humans. We found that HA functionalization increased stability and dispersion of MWCNTs and reduced postexposure lung inflammation, fibrosis, and mucus cell metaplasia compared with nonfunctionalized MWCNTs. Cocultures of fully differentiated bronchial epithelial cells (cultivated at air-liquid interface) and human lung fibroblasts (submerged) displayed significant reduction in injury, oxidative stress, as well as pro-inflammatory gene and protein expression after exposure to HA-functionalized MWCNTs compared with MWCNTs alone. In contrast, neither type of nanotubes stimulated cytokine production in primary human alveolar macrophages. In aggregate, our results demonstrate the effectiveness of HA functionalization as a safer design approach to eliminate MWCNT-induced lung injury and suggest that HA functionalization works by reducing MWCNT-induced epithelial injury.

Indexed as

Nanotubes, CarbonFibroblastsHumansHyaluronic AcidLungLung InjuryMacrophages, AlveolarMolecular WeightHyaluronic AcidNanotubes, Carbondifferentiated human bronchial epitheliafibrosishyaluronaninflammationlungmucous metaplasiamultiwalled carbon nanotubes

Identifiers

PMID27459049
PMCPMC5340294
OpenAlexW2493933247

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.