Jf. Vanstaden et al., DETERMINATION OF IRON(III) IN PHARMACEUTICAL SAMPLES USING DIALYSIS IN A SEQUENTIAL INJECTION-ANALYSIS SYSTEM, Analytica chimica acta, 357(1-2), 1997, pp. 141-149
The use of membranes for on-line separations in flow-through dialysers
as part of flow systems is extremely useful for automated sample prep
aration. Iron(III) was separated from a sample matrix by dialysis in a
sequential injection system. The dialysed iron was complexed with tir
on and the resulting complex was monitored spectrophotometrically at 6
67 nm. The influence of various parameters, including pump speed for b
oth the donor and recipient streams, sample volume, reagent volume, di
alysis time and the effect of multiple how reversals, on dialysis effi
ciency was studied. The system proved to be feasible for the determina
tion of iron in pharmaceutical samples which are usually turbid and co
ntain undissolved organic particles. The system is fully computerised
and is able to monitor iron(III) in samples at a frequency of 8 sample
s per hour with a relative standard deviation (RSD) of <1.50% in the l
inear calibration range (100-1000 mg l(-1)). The 3 sigma detection lim
it is 45.0 mg l(-1). Although the sample frequency of the proposed seq
uential injection system is much lower than that of conventional flow
injection systems, the volume of sample used is much smaller and the c
onsumption of reagents is much lower, which is more cost effective. Us
ing the feature of multiple flow reversals, the percentage dialysis ca
n be improved to up to 4.5%, which compares well with the 4% obtained
with conventional how injection analysis. (C) 1997 Elsevier Science B.
V.