Influence of particle size on persistence and clearance of aerosolized silver nanoparticles in the rat lung
-
2015/04/01
-
Details
-
Personal Author:Anderson DS ; Brown JM ; Chen LC ; Das GK ; Gordon T ; Guo T ; Patchin ES ; Pinkerton KE ; Shannahan J ; Sharmah A ; Silva RM ; Uyeminami DL ; Van Winkle LS
-
Description:The growing use of silver nanoparticles (AgNPs) in consumer products raises concerns about potential health effects. This study investigated the persistence and clearance of 2 different size AgNPs (20 and 110 nm) delivered to rats by single nose-only aerosol exposures (6 h) of 7.2 and 5.4 mg/m(3), respectively. Rat lung tissue was assessed for silver accumulations using inductively-coupled plasma mass spectrometry (ICP-MS), autometallography, and enhanced dark field microscopy. Involvement of tissue macrophages was assessed by scoring of silver staining in bronchoalveolar lavage fluid (BALF). Silver was abundant in most macrophages at 1 day post-exposure. The group exposed to 20 nm AgNP had the greatest number of silver positive BALF macrophages at 56 days post-exposure. While there was a significant decrease in the amount of silver in lung tissue at 56 days post-exposure compared with 1 day following exposure, at least 33% of the initial delivered dose was still present for both AgNPs. Regardless of particle size, silver was predominantly localized within the terminal bronchial/alveolar duct junction region of the lung associated with extracellular matrix and within epithelial cells. Inhalation of both 20 and 110 nm AgNPs resulted in a persistence of silver in the lung at 56 days post-exposure and local deposition as well as accumulation of silver at the terminal bronchiole alveolar duct junction. Further the smaller particles, 20 nm AgNP, produced a greater silver burden in BALF macrophages as well as greater persistence of silver positive macrophages at later timepoints (21 and 56 days). [Description provided by NIOSH]
-
Subjects:
-
Keywords:
-
ISSN:1096-6080
-
Document Type:
-
Funding:
-
Genre:
-
Place as Subject:
-
CIO:
-
Topic:
-
Location:
-
Pages in Document:366-381
-
Volume:144
-
Issue:2
-
NIOSHTIC Number:nn:20048463
-
Citation:Toxicol Sci 2015 Apr; 144(2):366-381
-
Contact Point Address:Laura S. Van Winkle, Department of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, One Shields Avenue, Davis, California 95616
-
Email:lsvanwinkle@ucdavis.edu
-
CAS Registry Number:
-
Federal Fiscal Year:2015
-
NORA Priority Area:
-
Performing Organization:University of California - Davis
-
Peer Reviewed:True
-
Start Date:20010930
-
Source Full Name:Toxicological Sciences
-
End Date:20270929
-
Collection(s):
-
Main Document Checksum:urn:sha-512:6e6bfde89c90eb9aa69f9b7d09198a821ad3df3123875a767dbd4475c6a46565e40836d5cec3a82d636cc699177dc44666c3bf4f21912b26234d6b622ea1aec4
-
Download URL:
-
File Type:
ON THIS PAGE
CDC STACKS serves as an archival repository of CDC-published products including
scientific findings,
journal articles, guidelines, recommendations, or other public health information authored or
co-authored by CDC or funded partners.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
You May Also Like