Skip directly to search Skip directly to A to Z list Skip directly to page options Skip directly to site content

NIOSHTIC-2 Publications Search

Search Results

Whole-body nanoparticle aerosol inhalation exposure.

Authors
Yi-J; Chen-BT; Schwegler-Berry-DE; Frazer-DG; Castranova-V; McBride-C; Knuckles-TL; Stapleton-PA; Minarchick-VC; Nurkiewicz-TR
Source
J Vis Exp 2013 May; 75:e50263
NIOSHTIC No.
20042823
Abstract
Inhalation is the most likely exposure route for individuals working with aerosolizable engineered nano-materials (ENM). To properly perform nanoparticle inhalation toxicology studies, the aerosols in a chamber housing the experimental animals must have: 1) a steady concentration maintained at a desired level for the entire exposure period; 2) a homogenous composition free of contaminants; and 3) a stable size distribution with a geometric mean diameter < 200 nm and a geometric standard deviation óg < 2.5 5. The generation of aerosols containing nanoparticles is quite challenging because nanoparticles easily agglomerate. This is largely due to very strong inter-particle forces and the formation of large fractal structures in tens or hundreds of microns in size 6, which are difficult to be broken up. Several common aerosol generators, including nebulizers, fluidized beds, Venturi aspirators and the Wright dust feed, were tested; however, none were able to produce nanoparticle aerosols which satisfy all criteria 5. A whole-body nanoparticle aerosol inhalation exposure system was fabricated, validated and utilized for nano-TiO2 inhalation toxicology studies. Critical components: 1) novel nano-TiO2 aerosol generator; 2) 0.5 m3 whole-body inhalation exposure chamber; and 3) monitor and control system. Nano-TiO2 aerosols generated from bulk dry nano-TiO2 powders (primary diameter of 21 nm, bulk density of 3.8 g/cm3) were delivered into the exposure chamber at a flow rate of 90 LPM (10.8 air changes/hr). Particle size distribution and mass concentration profiles were measured continuously with a scanning mobility particle sizer (SMPS), and an electric low pressure impactor (ELPI). The aerosol mass concentration (C) was verified gravimetrically (mg/m3). The mass (M) of the collected particles was determined as M = (Mpost-Mpre), where Mpre and Mpost are masses of the filter before and after sampling (mg). The mass concentration was calculated as C = M/(Q*t), where Q is sampling flowrate (m3/min), and t is the sampling time (minute). The chamber pressure, temperature, relative humidity (RH), O2 and CO2 concentrations were monitored and controlled continuously. Nano-TiO2 aerosols collected on Nuclepore filters were analyzed with a scanning electron microscope (SEM) and energy dispersive X-ray (EDX) analysis. In summary, we report that the nano-particle aerosols generated and delivered to our exposure chamber have: 1) steady mass concentration; 2) homogenous composition free of contaminants; 3) stable particle size distributions with a count-median aerodynamic diameter of 157 nm during aerosol generation. This system reliably and repeatedly creates test atmospheres that simulate occupational, environmental or domestic ENM aerosol exposures.
Keywords
Inhalants; Humans; Men; Women; Aerosols; Nanotechnology; Particulates; Toxicology; Animals; Laboratory-animals; Exposure-levels; Analytical-processes; Author Keywords: Medicine; Issue 75; Physiology; Anatomy; Chemistry; Biomedical Engineering; Pharmacology; Titanium dioxide; engineered nanomaterials; nanoparticle; toxicology; inhalation exposure; aerosols; dry powder; animal model
CODEN
JVEOA4
Publication Date
20130507
Document Type
Journal Article
Email Address
tnurkiewicz@hsc.wvu.edu
Fiscal Year
2013
NTIS Accession No.
NTIS Price
Identifying No.
B20130718
ISSN
1940-087X
NIOSH Division
HELD
Priority Area
Construction; Manufacturing
Source Name
Journal of Visualized Experiments
State
WV
TOP