Determination of cisapride, its oxidation product, propyl and butyl parabens in pharmaceutical dosage form by reversed-phase liquid chromatography.

Abstract:

:A simple, rapid and reproducible high-performance liquid chromatography (HPLC) assay for cisapride, its oxidation product (OP), propyl and butyl parabens in a pharmaceutical formulation is described. Chromatography was performed at room temperature by pumping acetonitrile-20 mM phosphate buffer pH 7 (50:50, v/v) at 1.5 ml min(-1) through C8 reversed-phase column. Cisapride, OP, propyl and butyl parabens were detected at 276 nm and were eluted at 9.7, 3.1, 5.1 and 7.1 min, respectively. Calibration plots were linear (r>0.999) for all compounds from 0.5 to 200 microg ml(-1) for cisapride and OP and 0.1-200 microg ml(-1) for propyl and butyl parabens. Detection limits for cisapride, OP, propyl and butyl parabens were 40, 46, 48 and 54 ng ml(-1), respectively. Forced degradation investigations showed that cisapride does not undergo degradation under heat, acidic and basic conditions but it was susceptible to oxidation. The proposed method was successfully applied to the assay of cisapride in the presence of preservatives and OP in a commercial suspension.

journal_name

J Pharm Biomed Anal

authors

Belgaied JE,Trabelsi H

doi

10.1016/s0731-7085(03)00421-7

subject

Has Abstract

pub_date

2003-12-04 00:00:00

pages

991-8

issue

5

eissn

0731-7085

issn

1873-264X

pii

S0731708503004217

journal_volume

33

pub_type

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