The degradation of ascorbic acid (AA) stored in parenteral nutrition (PN) r
egimens is initially by oxidation, catalysed by trace elements, in particul
ar copper. After prolonged storage the concentration of AA remains relative
ly constant, with little variation, due to the lack of available oxygen. Th
e initial degradation product is dehydroascorbic acid (DHAA). This is gener
ated in an anaerobic environment, and is hypothesised to degrade by hydroly
sis. It is the purpose of this investigation to ascertain the effect of tem
perature and trace elements on the anaerobic degradation of DHAA, and to id
entify the kinetics of the reaction. A stability-indicating reversed-phase
HPLC assay was used. The column contained C,, reverse-phase packing (Luna),
mean diameter 5 mum. The column dimensions were 15 cm long with an interna
l diameter of 0.4 cm. The mobile phase consisted of methanol: phosphate buf
fer (pH 7.8: 0.067 mol dm(-3)) at a ratio of 40: 60 (v/v) and also included
Cetrimide (mixed alkyltrimethylammonium bromide) (0.05 mol dm(-3)) as an i
on pair reagent. The flow rate was 0.7 ml min(-1) and detection was by ultr
a-violet light absorption at 278 nm. This assay was used to monitor the deg
radation rate of DHAA in PN mixtures with and without trace elements over a
range of temperatures (5-35 degreesC). Results indicated a first order rea
ction that was temperature-dependent but trace elements independent. (C) 20
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