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Biomedical subjects

H C Hansson

Publications and source records attributed to H C Hansson.

3 recordsLinked to original sources

Why do medical nebulizers differ in their output and particle size characteristics?

Previous work done on the characterisation of nebulizers has focused on gravimetrical output and particle/droplet size distribution at various air flow rates. This paper investigates six different nebulizers, with regard to droplet generation and separation properties, at a single air flow rate. Droplet generation and separation properties were measured with laser diffraction and impactor techniques. For each of the nebulizers the air velocity was calculated and both liquid and air volumetric flow rate was measured. The primary generated droplets (nebulizer without impaction baffle) had a mean size of between 15 microns and > 500 microns. The secondary generated droplets (nebulizer with baffle) were in the size range of 1 to 10 microns. It was found that the baffle system of the investigated nebulizers could be described according to ordinary impaction theory. The mass median diameters (MMD) of these nebulizers were found to be dependent on air velocity (vg), and ratio of liquid to air volumetric flow rate (Ql/Qa). In all of the nebulizers, between 93% and 99% of the generated primary droplets were caught by the baffle system which resulted in a very low output. Thus, the nebulizers examined do not appear to be optimised, with regard to observed droplet generation and baffle arrangements, if secondary droplets with a size approximately 1 micron are desired. By changing the design at the primary generation point, air velocity (vg) and liquid to air flow rate (Ql/Qa), the primary generated droplet size could be decreased. This would result in an increase in the number concentration of smaller droplets that pass the baffle system.(ABSTRACT TRUNCATED AT 250 WORDS)

Equipment Design↗

Personal size-separating impactor for sampling microbiological aerosols.

A commercially-available personal impactor was altered to sample viable microorganisms onto a semisolid, moist, gelatin medium rather than onto a stainless steel or filter surface. The Marple personal cascade impactor is an eight-stage sampler with predicted cut-offs of 20, 15, 10, 6, 3.5, 2, 1, and 0.61 microns for stages one to eight, at a flow rate of 2 L/min. The possibility was examined that using trays containing a small amount of gelatin medium in place of the thin, flat filters of the original design would alter the impactor's performance. A polydisperse aerosol of di-2-ethylhexyl phthalate (DEHP or DOP) was sampled directly into an aerodynamic particle sizer and through a stage of the personal impactor. The aerosol particles penetrating the tested stage were sized and counted, and the counts compared with those in the total aerosol. With a Mylar medium filter as the collecting substrate, the measured particle cut-offs (D50) for stages four to seven were 5.2, 3.4, 1.4, and 1.0 microns. With a tray containing gelatin as the collecting substrate, the D50 were 5.9, 4.0, 1.6, and 1.0 microns. The size separation of the personal sampler for ambient bacterial and fungal aerosols compared well with that of the Andersen microbiological impactor. The use of a moist collecting surface, compared to a dry surface, can be expected to enhance recovery of viable airborne microorganisms sensitive to dehydration.

Aerosols↗

Investigations into whether 5-hydroxytryptamine is a neurotransmitter in the retina of rabbit and chicken.

A system of indoleamine-accumulating neurons exists in the retina of several species, but the exact transmitter of these neurons is not known. 5-Hydroxytryptamine (5-HT) is a likely candidate, but there are conflicting reports on its amount in the retina. We have determined the amounts of 5-HT with two sensitive, specific, and independent methods. Because the content was found to be lower than what was expected for a neurotransmitter, the rate-limiting enzyme in the 5-HT synthesis was also estimated, as was the effect of 5-HT on cyclic AMP content of the retina. In the rabbit the 5-HT content was found to be 25 to 35 ng/gm wet weight, with not difference between light- and dark-adapted animals. There was no detectable activity of the rate-limiting enzyme tryptophan hydroxylase. It was not possible to raise the 5-HT concentration by treating the rabbits with a monoamine oxidase inhibitor and L-tryptophan. 5-HT induced no change in the cyclic AMP content of the rabbit retina. In both newly hatched and older chicken retina, the 5-HT concentration was higher than in rabbit. The 5-HT concentrations in all retinas were lower than would be expected for a monoamine neurotransmitter, and these results argue against 5-HT being the neurotransmitter of the indoleamine-accumulating neurons.

Adenosine Monophosphate↗