SPECTROPHOTOMETRIC DETERMINATION OF NICOTINE IN CIGARETTE TOBACCO AND BIOLOGICAL SAMPLES OF SMOKERS
Hany A. Omara* and Salma M. M. Attaf
ABSTRACT
A new simple, accurate, sensitive and economical procedure for the
estimation of nicotine (indirect) methods (A and B) for the
determination of nicotine in bulk sample and in biological samples are
described. The first method is based on the oxidation of nicotine by Nbromosuccinimide
(NBS) and determination of the unreacted NBS by
measurement of the decrease in absorbance of methyl orange dye
(MO) at a suitable λmax = 507 nm. The absorbance concentration plot is
linear over the range (0.1-4.8 μg/ml). The second method is based on
oxidation of nicotine by cerric sulphate in acidic medium, and
determination of the unreacted oxidant by measuring the decrease in absorbance using
amaranth dye; (AM) at a suitable λmax (530 nm), respectively. Regression analysis of Beer's
law plots showed good correlation in the concentration ranges (0.3-5.9 μg/ml), respectively.
The limits of detection as well as quantification are reported. Sex replicate analyses (n=6) of
solutions containing three different concentrations of nicotine was carried out. The percent
error and the RSD values have been reported. The proposed methods were applied to the
determination of nicotine in cigarette tobacco present in Libya and in biological samples
(spiked human plasma and urine) and the results demonstrate that the method is equally
accurate and precise as found from the t- and F-values. The reliability of the method was
established by recovery studies using standard-addition technique.
Keywords: Nicotine; Spectrophotometry; Oxidation reaction; N-bromosuccinimide; Cerric sulphate, Cigarette tobacco in Libyan markets; Spiked human plasma and Urine.
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