ملخص
A simple, rapid and sensitive method has been developed for the analysis of fexofenadine (FEX) in pharmaceutical
formulations, using a tris(1,10‐phenanthroline)–ruthenium(II) [Ru(phen)3
2+] peroxydisulphate chemiluminescence (CL) system in
a multichip device. Various parameters that influence the CL signal intensity were optimized. These included pH, flow rates and
concentration of reagents used. Under optimumconditions, a linear calibration curve in the range 0.05–5.0 μg/mL was obtained.
The detection limit was found to be 0.001 μg/mL. The procedure was applied to the analysis of FEX in pharmaceutical products
and was found to be free from interference from concomitants usually present in these preparations.
formulations, using a tris(1,10‐phenanthroline)–ruthenium(II) [Ru(phen)3
2+] peroxydisulphate chemiluminescence (CL) system in
a multichip device. Various parameters that influence the CL signal intensity were optimized. These included pH, flow rates and
concentration of reagents used. Under optimumconditions, a linear calibration curve in the range 0.05–5.0 μg/mL was obtained.
The detection limit was found to be 0.001 μg/mL. The procedure was applied to the analysis of FEX in pharmaceutical products
and was found to be free from interference from concomitants usually present in these preparations.
اللغة الأصلية | English |
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الصفحات (من إلى) | 762–767 |
عدد الصفحات | 6 |
دورية | Journal of Bioluminescence and Chemiluminescence |
حالة النشر | Published - 2011 |