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Dry cell weight (DCW) was measured by filtering 5 mL of culture broth through a 0.45 μm nitrocellulose filter and measuring the increased weight of the dry filter.
TPM concentrations were monitored by drawing sample air from the exposure chamber through a quartz fibre filter and measuring the total air volume.
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Albuterol was collected with a filter and measured the percent amount delivered by infrared spectrophotometry.
There was a strong correlation between creatinine clearance by the filter and measured drug clearance (P < 0.001).
The scattering beam from the sample plane is collected by a condenser lens and reduced in the intensity using a neutral density filter and measured by an avalanche photodiodes (Hamamatsu, G8931-04) monnted on a manual stage.
The sensitivity of the SUVref methodology to filter size was assessed by applying non-optimal SUVref filters and measuring the effect on Δ SUVref.
The dry weight concentration was determined by filtrating culture broth over preweighted glass fiber filters and measuring the weight increase of the filters after drying at 95°C as described by Kliphuis et al. [ 43].
Optical power density of the light flux was varied from 2 to 170 mW/cm2 by means of neutral density filters and measured by a Laser Precision Rk-5720 poweradiometereradiometer
The level of trans-illumination was controlled by neutral density filters and measured in situ at the gratings.
Samples were collected using 37-mm quartz filters and measured particulate-phase PAHs only.
Cell culture supernatants were harvested from these transfections, filtered, and measured for infectious units via infection of TZMbl cells.
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