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1.
J Fluoresc ; 25(6): 1577-84, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26438658

ABSTRACT

A novel, simple and specific spectrofluorimetric method was developed and validated for the determination of perindopril erbumine (PDE). The method is based on the fluorescence quenching of Rhodamine B upon adding perindopril erbumine. The quenched fluorescence was monitored at 578 nm after excitation at 500 nm. The optimization of the reaction conditions such as the solvent, reagent concentration, and reaction time were investigated. Under the optimum conditions, the fluorescence quenching was linear over a concentration range of 1.0-6.0 µg/mL. The proposed method was fully validated and successfully applied to the analysis of perindopril erbumine in pure form and tablets. Statistical comparison of the results obtained by the developed and reference methods revealed no significant differences between the methods compared in terms of accuracy and precision. The method was shown to be highly specific in the presence of indapamide, a diuretic that is commonly combined with perindopril erbumine. The mechanism of rhodamine B quenching was also discussed.


Subject(s)
Perindopril/analysis , Rhodamines/chemistry , Spectrometry, Fluorescence/methods , Linear Models , Perindopril/chemistry , Solvents/chemistry , Temperature , Time Factors
2.
J Fluoresc ; 25(4): 811-8, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26149499

ABSTRACT

A novel, simple, selective and sensitive spectrofluorimetric method was developed and validated for the determination of perindopril erbumine using 7-hydroxycoumarin. Perindopril erbumine was found to react with 7-hydroxycoumarin in acetonitrile resulting in a new fluorescent product with about 58 nm blue shifted emission. The fluorescence of the complex was measured at 440 nm after excitation at 350 nm in acetonitrile. Under the optimum conditions, the fluorescence intensity was linear over a concentration range of 2.0-16.0 µg/mL (R(2) = 1) with a detection limit of 0.054 µg/mL. The proposed method was fully validated and successfully applied to the analysis of perindopril erbumine in pure form and tablets. Statistical comparison of the results obtained by the proposed and reference method revealed no significant differences in the performance of the two methods regarding the accuracy and precision respectively. The method was shown to be highly specific in the presence of indapamide, a diuretic that is commonly combined with perindopril erbumine. A proposal for the reaction pathway with 7-hydroxycoumarin was postulated.


Subject(s)
Acetonitriles/chemistry , Perindopril/analysis , Spectrometry, Fluorescence/methods , Tablets/analysis , Umbelliferones/chemistry , Fluorescence , Hydrogen-Ion Concentration , Limit of Detection , Reproducibility of Results
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