Rapid and Sensitive Online Determination of Some Selective I-1-Blockers by Flow Injection Analysis with Micelle-Enhanced Fluorescence Detection

A rapid, sensitive and selective flow injection analysis (FIA) method was developed for the determination of some selective I-1-blockers including; terazosin (TER), doxazosin (DOX), prazosin (PRZ), and alfuzosin (ALF). The method was based on enhancement of the native fluorescence of the studied dru...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of fluorescence 2013-11, Vol.23 (6), p.1301-1311
Hauptverfasser: Mohamed, Niveen, Ahmed, Sameh, Zohny, Sally
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:A rapid, sensitive and selective flow injection analysis (FIA) method was developed for the determination of some selective I-1-blockers including; terazosin (TER), doxazosin (DOX), prazosin (PRZ), and alfuzosin (ALF). The method was based on enhancement of the native fluorescence of the studied drugs in the presence of sodium dodecyl sulfate (SDS). The method was optimized for the buffer type, concentration and pH, surfactant type and concentration, flow rate and detection wavelengths in order to achieve the maximum sensitivity. The results showed that the best sensitivity was obtained by using SDS (10 mM) in phosphate buffer (20 mM, pHa=a3), flow rate was 0.5 ml/min and the detector was set at I>exa=a250 and I>ema=a389. Under these optimum conditions there was a linear relationship between the concentration and the fluorescence intensity in the range from 5a400 ng mla with correlation coefficient of more than 0.998. The detection and quantitation limits for the studied drugs by the proposed method were 3.2a11.9 ng mla1 and 10.8a39.7 ng mla1, respectively. The method was validated in accordance with the requirements of ICH guidelines and shown to be suitable for intended applications. Moreover, the binding constants for I-1ablockers aSDS system were determined using the adduct model. The proposed method has been applied successfully for the analysis of the pure forms for studied drugs and also their pharmaceutical formulations and the results were compared with official methods.
ISSN:1053-0509
1573-4994
DOI:10.1007/s10895-013-1264-0