Abstract:
A rapid, simple, accurate, and precise method for the determination of propyl paraben,
methyl paraben, sodiumbenzoate, and bronopol in Polyherbal cough syrup by means of
reverse phase high performance liquid chromatography coupled to UV detector was
developed. Best separation was achieved using a Phenomenex Luna C18(2) (250 mm × 4.60
mm, with particle size of 5 μm) as well as isocratic elution consisting of sodium dihydrogen phosphate buffer/ acetonitrile (63:37) at pH 4.0 adjusted with ortho phosphoric acid at a flow
rate of 1.5 mL/min. The optimized and applied chromatographic conditions permitted
separation of Propylparaben, Methylparaben, Sodiumbenzoate, and Bronopol from
interacting matrix with good sensitivity. The method validation was carried out with regard to
the guidelines for analytical procedures demanded by the International Conference on
Harmonisation (ICH). Limits of detection was found to be 2.21μg/mL, 5.54μg/mL,
0.34μg/mL, 0.46μg/mL and LOQ was found to be 3.72 μg/mL, 16.08μg/mL, 1.07μg/mL,
1.39μg/mL for Bronopol, Sodiumbenzoate, Methyl paraben, Propyl paraben respectively.
Retention time of Bronopol, Sodiumbenzoate, Methylparaben, Propylparaben obtained was
2.5, 4.4, 5.05, 13.6 minutes respectively. Specificity experiments revealed the absence of
interference from excipients, interacting matrix could be eliminated by the chromatographic
procedure with excellent performance of system suitability having RSD≤2 for all four
analytes. The linearity was found to be in the range of 2-30μg/mL, 66-990μg/mL, 26-
390μg/mL, 5-78μg/mL for Bronopol, Sodiumbenzoate, Methylparaben, Propylparaben
respectively. Accuracy was achieved with %recovery within 98%-102% for all preservatives.
Analysis of marketed formulation gives %assay results of 98.99±0.58, 98.54±0.72,
98.27±0.445, and 100.54±0.27 for Bronopol, Sodiumbenzoate, Methylparaben,
Propylparaben respectively.
