Evidence map›Paper›PMID 30616672›Full record

ArticleParticle and fibre toxicology2019

Lobar evenness of deposition/retention in rat lungs of inhaled silver nanoparticles: an approach for reducing animal use while maximizing endpoints.

Jung Duck Park, Jin Kwon Kim, Mi Seong Jo, Young Hun Kim, Ki Soo Jeon, Ji Hyun Lee, Elaine M Faustman, Hong Ku Lee, Kangho Ahn, Mary Gulumian and 2 more

Abstract read
In one paragraph

Article in Particle and fibre toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Nanotechnology-based mRNA vaccines.Nature reviews. Methods primers · 2023
    Article
  5. Article
  6. Article
  7. Article
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

12 authors.

Jung Duck ParkDeparment of Preventive Medicine College of Medicine, Chung-Ang University, Seoul, South Korea.
Jin Kwon KimDepartment of Nanofusion Technology, Hoseo University, Asan, South Korea.
Mi Seong JoDepartment of Nanofusion Technology, Hoseo University, Asan, South Korea.
Young Hun KimHCTm CO.,LTD, Seoicheon-ro 578 beon-gil, Majang-myeon, Icheon, 17383, South Korea.
Ki Soo JeonHCTm CO.,LTD, Seoicheon-ro 578 beon-gil, Majang-myeon, Icheon, 17383, South Korea.
Ji Hyun LeeDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, USA.
Elaine M FaustmanDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, USA.
Hong Ku LeeDepartment of Mechanical Engineering, Hanyang University, Ansan, South Korea.
Kangho AhnDepartment of Mechanical Engineering, Hanyang University, Ansan, South Korea.
Mary GulumianNational Institute for Occupational Health, University of the Witwatersrand, Johannesburg, South Africa.
Günter OberdörsterDepartment of Environmental Medicine, University of Rochester, Rochester, NY, USA.
Il Je YuHCTm CO.,LTD, Seoicheon-ro 578 beon-gil, Majang-myeon, Icheon, 17383, South Korea. u1670916@chollian.net.

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Project 3: Integrative Risk Assessment Methods for Engineered NanomaterialsU19ES019545 · NIEHS · UNIVERSITY OF WASHINGTON · PI KAVANAGH, TERRANCE J · 2010 to 2014
$5.6M
Korea Evaluation Institute of Industrial Technology 10052901NIEHS NIH HHS P30 ES007033NIEHS NIH HHS U19 ES019545U.S. Environmental Protection Agency RD83573801
6 · The paper itself

Abstract

backgroundInformation on particle deposition, retention and clearance are important for the evaluation of the risk of inhaled nanomaterials to human health. Recent revised OECD inhalation toxicity test guidelines require to evaluate the lung burden of nanomaterials after rodent subacute and subchronic inhalation exposure (OECD 412, OECD 413). These revised test guidelines require additional post-exposure observation (PEO) periods that include lung burden measurements that can inform on lung clearance behavior and translocation. The latter being particularly relevant when the testing chemical is a solid poorly soluble nanomaterial. Therefore, in the spirit of 3 R's, we investigated whether measurement of retained lung burden of inhaled nanoparticles (NPs) in individual lung lobes is sufficient to determine retained lung burden in the total lung. If it is possible to use only one lobe, it will reduce animal use and maximize the number of endpoints evaluated.

resultsTo achieve these goals, rats were exposed nose-only for 1 or 5 days (6 h/day) to an aerosol of 20 nm well-dispersed silver nanoparticles (AgNPs), which is the desired particle diameter resulting in maximum deposition in the pulmonary region when inhaled as singlets. After exposure, the five lung lobes were separated and silver concentration was measured using inductively coupled plasma-mass spectrophotometer (ICP-MS). The results showed that the retention of deposited silver nanoparticle in the different lung lobes did not show any statistically significant difference among lung lobes in terms of silver mass per gram lung lobe. This novel finding of evenness of retention/deposition of inhaled 20 nm NPs in rats for all five lobes in terms of mass per unit tissue weight contrasts with earlier studies reporting greater apical lobe deposition of inhaled micro-particles in rodents. The difference is most likely due to preferred and efficient deposition of inhaled NPs by diffusion vs. additional deposition by sedimentation and impaction for micron-sized particles.

conclusionAgNPs following acute inhalation by rats are evenly retained in each lung lobe in terms of mass per unit lung tissue weight. Accordingly, we suggest sampling any of the rat lung lobes for lung burden analysis can be used to determine deposited or retained total lung burden after short-term inhalation of NPs and using the other lobes for collecting and analyzing bronchoalveolar lavage fluid (BALF) and for histopathological analysis. Therefore, by combining lung burden measurement, histopathological tissue preparation, and BALF assay in the same rat will reduce the number of animals used and maximize the number of endpoints measured.

Indexed as

Animal Use AlternativesEndpoint DeterminationLungAcinar CellsAnimalsBiomarkersBody BurdenBronchoalveolar Lavage FluidInhalation ExposureMaleMetal NanoparticlesOrgan SizeRats, Sprague-DawleySilverTissue DistributionBiomarkersSilver

Identifiers

PMID30616672
PMCPMC6322301

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Registered trials

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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.