H. Pasekova et al., Potentiometric determination of acetylsalicylic acid by sequential injection analysis (SIA) using a tubular salicylate-selective electrode, J PHARM B, 24(5-6), 2001, pp. 1027-1036
This paper deals with the development of an automated procedure for formula
tion assays and dissolution tests based on a sequential injection analysis
(SIA) system involving an ion-selective electrode as sensing device. Constr
uction of a tubular salicylate (Sal) selective electrode suitable for poten
tiometric determination of acetylsalicylic acid (Asa) in pharmaceutical for
mulations is described. The flow-through electrode is formed by a PVC membr
ane containing 29.2% (w/w) PVC, 5.8% (w/w) tetraoctylammonium salicylate (i
onic sensor), 58.5% o-nitrophenyloctylether (plasticizer) and 6.5% (w/w) p-
tert-octylphenol (stabilising, additive which increases electrode selectivi
ty). The calibration range is 0.05-10 mM Sal, the limit of detection (LOD)
is 0.05 mM Sal, the slope is 56.0 mV per decade at 22 degreesC. The R.S.D.
is 0.20% (15 readings) when determining 2.5 mM Sal in standard solution. Th
e electrode is used fur sensing Asa after. its on-line chemical hydrolysis
to Sal in a SIA system. The sampling rate is 6 h(-1) but for the dissolutio
n tests the frequency is increased to 20 h(-1). The SIA set-up is employed
for the assay of Asa in plain tablets, composed tablets and effervescent ta
blets and for performing dissolution tests of normal and sustained release
tablets. Results obtained by this technique compare well with those require
d by the US Pharmacopoeia XXIV. (C) 2001 Elsevier Science B.V. All lights r
eserved.