Determination of Orciprenaline Using a Flow Injection Analysis System with Sequential Potentiometric and Spectrophotometric Detection

Author: El Nashar Rasha  

Publisher: Taylor & Francis Ltd

ISSN: 0003-2719

Source: Analytical Letters, Vol.41, Iss.6, 2008-04, pp. : 949-964

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

This work describes an attempt to have a flow injection analysis (FIA) system for Orciprenaline with potentiometric and spectrophotometric detectors working sequentially. The potentiometric detection was performed using an orciprenaline ion-selective electrode made of orciprenaline ion-associate with phosphotungstic acid incorporated in a PVC matrix membrane, followed by sequential spectrophotometric detection of the same sample using the reaction of orciprenaline with phosphomolybdic acid in alkaline medium and measurement at 670 nm using a USB2000 fiber-optic spectrophotometer. The method was applied and validated for the assay of different samples that are 1.0 × 10-2-1.0 × 10-7 M orciprenaline, and the recovery values for Alupent® tablets, plasma and urine sample ranged from 99.39-100.93, 99.87-100.57, and 98.83-100.64 respectively for the potentiometric detector and 99.66-100.58, 99.78-100.69 and 99.12-100.92 respectively for the sequential spectrophotometric detector. It was found that using the double detection system compensated for both the unselectivity of the spectrophotometric method and the low detection limit of the potentiometric method (6.3 × 10-4 M). Although two detectors were used in the measurements, the method is still very simple to design and apply, in addition to being rapid and less expensive than other more sophisticated techniques applied in the literature and can therefore be used for other pharmaceutical compounds as well.

Related content