A new method for quantifiable and controlled dosage of particulate matter for in vitro studies: the electrostatic particulate dosage and exposure system (EPDExS).

An exposure chamber is described for the quantifiable addition of fine and ultrafine aerosol particulate matter directly to cells and used to demonstrate the in vitro cytotoxicity of fine 1,4-naphthoquinone particles to murine lung epithelial cells. The electrostatic particulate dosage and exposure system (EPDExS) operates on the principle of electrostatic precipitation and is shown to deposit fine and ultrafine aerosol particles directly to cells with 100% efficiency for particle diameters in the range of 40-530nm. This range is not limited by the EPDExS, but rather by the aerosolization method used for this study. Numbers of particles deposited onto the cells are counted with a condensation particle counter, negating any need to calculate or estimate particle exposure. The process of particle introduction, assessed using Trypan blue dye exclusion, had no effect on cell viability. In combination with a differential mobility classifier, the EPDExS can deliver select particle diameters to cells. The ability to control the diameter and number of particles deposited permits in vitro toxicity studies of particulate matter using different particle dosage metrics, i.e., particle number and size, surface area and mass. Finally, because EPDExS introduces particles directly from the aerosol, it can be used to expose cells grown at air/liquid interfaces.

Investigation of factors that affect the sensitivity of accelerator mass spectrometry for cosmogenic 10Be and 26Al isotope analysis.

We report experiments designed to improve accelerator mass spectrometry (AMS) of (10)Be and (26)Al for a wide range of geological applications. In many cases, the precision of the AMS isotope ratio measurement is restricted by counting statistics for the cosmogenic isotope, which are in turn limited by the intensity of AMS stable ion beam currents. We present data obtained at the Center for Accelerator Mass Spectrometry (CAMS) at Lawrence Livermore National Laboratories (LLNL) indicating that AMS ion beam currents are impacted by certain elemental impurities. For (10)Be analysis, the AMS ion beam current is most adversely affected by the presence of titanium (which can be challenging to separate chemically during sample preparation because of its tendency toward stable refractory forms) and aluminum (which can coelute with beryllium during cation exchange chromatography). In order to minimize impurities that suppress AMS ion beam currents, we evaluate, using inductively coupled plasma atomic emission spectroscopy (ICP-AES), a widely used chemical separation protocol involving a multiacid digestion scheme, preseparation elemental analysis, anion exchange chromatography, ad hoc selective precipitation, cation exchange chromatography, and postseparation elemental analysis.

Absolute and/or relative detection limits in laser-based analysis: the end justifies the means.

The absolute limit of detection usually expresses the minimum amount of analyte detectable, while the relative limit of detection refers to the minimum concentration of analyte detectable. These concepts and their differences are obviously familiar to all analytical spectroscopists. Nevertheless, the two definitions are used liberally in the literature. For example, it is not uncommon to refer to exceptional sub-femtograms detection limits for a technique used to analyse ultratrace levels of an element in water and to a modest part per million detection limit of another technique used to characterise the microdistribution of an element in a sample mass of about one microgram. In this paper, an attempt is made to point out that the terms "ultratrace analysis" and "microanalysis" must refer to two conceptually different approaches and that there are cases in which one definition is more appropriate than the other. It is argued that, while there is no objection in reporting both detection limits when a single technique is evaluated, one has to be careful in choosing the most appropriate definition when different analytical techniques are compared.

Determination of ultra-trace levels of gold in size-segregated atmospheric particulate samples by laser induced fluorescence: towards an aerosol tracer.

A method is described for measuring the gold content of integral and size-segregated samples of atmospheric particulate matter. After acid digestion and a liquid/ liquid extraction, the sample are analysed by Two-Colour Laser Induced Fluorescence in a graphite furnace. An absolute instrumental detection limit of 1 fg is achieved. Assuming a sampled volume of 1 m(3), this corresponds to an atmospheric concentration of 50 fg m(-3). Due to blank limited noise, the above limits increase to 20 fg and 1 pg m(-3), respectively. Results of the analysis of filter samples as well as of size-segregated impactor samples are presented.

Ground state saturated population distribution of OH in an acetylene-air flame measured by two optical double resonance pump-probe approaches.

Two optical double-resonance pump-probe techniques were used to determine the ground-state rotational population distributions of OH in an acetylene-air flame when a saturating laser beam is tuned to the Q(1)4 transition of the (0, 0) Sigma-II band. The saturated absorption technique is based on the detection of absorption by a probe laser under conditions of saturation with a pump laser and no saturation. In the fluorescence technique, a probe laser is scanned through the (1, 0) band, while a saturating pump laser, tuned to the (0, 0) band, is on or off. We found that approximately 15% of the total population of the ground state was transferred to the excited state. Perturbation of the rotational population distribution was greater for rotational levels close to the directly excited laser-coupled level. The rotational energy transfer rate in the ground state was somewhat greater than in the excited state. The assumption of the balanced cross-rate model was verified as a means of determining the absoslute OH number density with adequate accuracy.