Characterization of Airborne Particles Emitted During Application of Cosmetic Talc Products.

A pilot study was undertaken to characterize the concentration, duration and particle size distribution of the talc cloud that forms in the personal breathing zone (PBZ) during application of certain talc-containing cosmetics. Multiple direct-reading instruments were employed to simultaneously monitor PM4 concentrations (particulate matter with aerodynamic diameter < 4 µm; mg/m3) at different distances from each of three subjects while they applied talc products. Results indicated that the purpose and method of applying the talc product, combined with behavioral and physical differences amongst subjects, all strongly influenced airborne talc concentrations and the duration of the cloud. Air concentrations of talc in the PBZ averaged around 1.0 mg/m3, and the duration of exposure varied from less than one minute to more than ten minutes. The real-time monitors captured the occasional formation of secondary clouds, likely caused by resuspension of talc particles from skin or other surfaces. Measurements of aerosolized baby powder, face powder, and two adult body powders indicated that the median aerodynamic diameter of the talc cloud ranged from 1.7 to 2.0 µm. These direct-reading approaches were valuable for providing detailed characterization of short duration exposures to airborne talc particles, and will be useful to support future exposure assessments of talc and other powders in consumer products.

Spatial and temporal variability of incidental nanoparticles in indoor workplaces: impact on the characterization of point source exposures.

This study deployed a suite of direct-reading instruments in six locations inside one building to characterize variability of the background aerosol, including incidental nanoparticles (NP), over a six month period. The instrument suite consisted of a portable Condensation Particle Counter (CPC) and a Scanning Mobility Particle Sizer (SMPS) for assessing particle number concentrations and size distributions in the nano-scale range; an Aerodynamic Particle Sizer (APS) for assessing micron-scale particle number concentrations and size distributions; plus a desktop Aerosol Monitor (DustTrak DRX) and a Diffusion Charger (DC2000CE) for assessing total particle mass and surface area concentrations respectively. In terms of number concentration, NPs (<100 nm) were the dominant particles observed in the background aerosol, contributing up to 53-93% of the total particle number concentrations. The particle size distributions were bimodal with maxima around 19-79 nm and 50-136 nm, respectively, depending on workplace locations. The average detected background particle number, surface area and total mass concentrations were below 7.1 × 10(3) # cm(-3), 22.9 µm(2) cm(-3) and 33.5 µg m(-3), respectively in spring samples and below 1.8 × 10(3) # cm(-3), 10.1 µm(2) cm(-3) and 12.0 µg m(-3), respectively in winter samples. A point source study using an older model laser printer as the emission source indicated that NPs emitted from the investigated printer were distinguishable from background. However, more recent low emitting printers are likely to be indistinguishable from background, and chemical characterization (e.g. VOCs, metals) would be required to help identify emission sources.

Continuous dielectrophoretic cell separation microfluidic device.

We present a prototype microfluidic device developed for the continuous dielectrophoretic (DEP) fractionation and purification of sample suspensions of biological cells. The device integrates three fully functional and distinct units consisting of an injector, a fractionation region, and two outlets. In the sheath and sample injection ports, the cell sample are hydrodynamically focused into a stream of controlled width; in the DEP fractionation region, a specially shaped nonuniform (isomotive) electric field is synthesized and employed to facilitate the separation, and the sorted cells are then delivered to two sample collection ports. The microfluidic behavior of the injector region was simulated and then experimentally verified. The operation and performance of the device was evaluated using yeast cells as model biological particles. Issues relating to the fabrication and operation of the device are discussed in detail. Such a device takes a significant step towards an integrated lab-on-a-chip device, which could interface/integrate to a number of other on-chip components for the device to undertake the whole laboratory procedure.