K. Kovacshadady et I. Fabian, THE DETERMINATION OF BENZALKONIUM CHLORIDE IN EYE-DROPS BY DIFFERENCESPECTROPHOTOMETRY, Journal of pharmaceutical and biomedical analysis, 16(5), 1998, pp. 733-740
A direct, extraction-free spectrophotometric method was developed for
the determination of benzalkonium chloride (BAC) in various eye-drops.
The procedure is based on ion-pair formation between BAC and 2',4',5'
,7'-tetrabromofluorescein (eosin-Y) which decreases the absorbance and
induces a bathochromic shift of the maximum in the eosin-Y spectrum.
The effects of pH, excess of reagent and ionic strength on the ion-pai
r formation have been studied in detail. At pH 4.40 and 9.62, the work
ing curve is linear in the 1.98 x 10(-6) to 2.40 x 10(-5) M (0.7-8.5 m
u g cm(-3)) concentration range; however, the sensitivity drops to abo
ut one third in the basic solution. At pH 4.40, the analytical signal
is stable for more than 60 min, while at pH 9.62 the signal changes in
time and reaches the maximum value 3 min after mixing the reagent and
the sample. When the active substance is beta-5-isopropyl-2'deoxyurid
ine and the sample contains typical additives, the reproducibility of
the analytical signal at pH 4.40 is R.S.D. = 2.36% (n = 81). In the ca
se of such samples, the linearity of the method is somewhat dependent
on the composition, but generally acceptable at the 50-150% concentrat
ion levels. Eye-drops containing tobramycin, an aminoglycoside-type an
tibiotic, as the active substance were analyzed at pH 9.62. This was n
ecessary to avoid strong interference from the analyte in acidic solut
ion. In this case the linearity of the method is limited to a narrower
concentration range however, the recovery is still acceptable at the
100% level. (C) 1998 Elsevier Science B.V.