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amplified and detected as a current. As mentioned in the previous chapter, the dark current <strong>of</strong><br />

the photomultiplier can be affected by changes in temperature and this model had an inbuilt<br />

cooler that kept the photomultiplier temperature at -200C to improve the signaUnoise ratio.<br />

<strong>The</strong> machine itself should ideally also be kept in a temperature controlled room (as was<br />

suggested in the machine manual). In our case it was placed in a small air conditioned room<br />

within the hospital away from any other equipment that potentially generated heat - though<br />

there was one window into the room which resulted in some temperature change. <strong>The</strong> NO<br />

analyser was re-serviced just prior to our experiments taking place.<br />

<strong>The</strong> NO analyser was calibrated with azero and two known NO gas concentrations before and<br />

after every subject during the methodological studies and between every two subjects when<br />

later studies in children were being undertaken. Two <strong>of</strong> the gases used were commercial<br />

preparations <strong>of</strong> NO made for calibration purposes by BOC Gases (BOC Gases, 10 Priestley<br />

Rd, Surrey Research Park, Guildford, Surrey, UK) and as the studies progressed included<br />

concentrations <strong>of</strong> 37ppb, 55ppb lO3ppb, l lOppb and I lSppb with the balance being nitrogen<br />

(Nz). Calibration gases at these low levels were extremely difficult to get at the<br />

commencement <strong>of</strong> these studies as these gas mixtures had no known use other than<br />

calibration, and this was not widely used at this time. <strong>The</strong> third gas was a zero calibration and<br />

this was prepared by passing room air through the ozone generator <strong>of</strong> the chemiluminescence<br />

analyser, which converted all NOx to NOz. This was then passed through a soda lime and<br />

activated charcoal column to remove the NOz and Ot respectively and then passed direct into<br />

the analyser. <strong>The</strong> resulting NOz and 03 from the experiment were removed in the same<br />

manner by passing through the soda lime column and the charcoal column. To minimise NO<br />

loss by absorption or interaction with other surfaces (see Section 5.4), teflon tubing (4mm<br />

extemal diameter) was used as the most inert substance to connect the machinery and to<br />

sample from the subject.<br />

5.2.2 Capnograph, pressure transducer, Jlow meter and chart recorder<br />

In addition to measuring NO itself, we wanted to be able to measure other parameters. At the<br />

time, the early publications available on exhaled NO from the lung, which will be reviewed in<br />

the next chapter (see Section 6.3), seemed to show a consistency in the trends found in NO<br />

results in different subject groups but the absolute levels <strong>of</strong> NO reported between the<br />

investigators were very different. This suggested that some <strong>of</strong> the measurement techniques<br />

were altering the NO results recorded. <strong>The</strong>re was also discussion in the literature about where<br />

the measured NO from exhalation was anatomically being generated. In view <strong>of</strong> this, we<br />

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