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1.
Luminescence ; 30(7): 1094-100, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25691393

RESUMO

A new method using chemiluminescence (CL) detection has been developed for the simple determination of ketotifen fumarate (KF). The method is based on the catalytic effect of KF in the CL reaction of tris(1,10 phenanthroline)ruthenium(II), Ru(phen)3 (2+), with Ce(IV) in sulfuric acid medium. The CL response was detected using a lab-made chemiluminometer. Effects of chemical variables were investigated and under optimum conditions, the CL intensity was proportional to the concentration of the drug over the range 0.34-34.00 µg mL(-1) KF. The limit of detection (S/N=3) was 0.09 µg mL(-1). Effects of common ingredients were investigated and the method was applied successfully for determining KF in pharmaceutical formulations and human plasma. The percent of relative standard deviation (n=11) at level of 3.4 µg mL(-1) of KF was 4.6% and the minimum sampling rate was 70 samples per hour. The possible CL mechanism is proposed based on the kinetic characteristic of the CL reaction, CL spectrum, UV-Vis and phosphorescence spectra.


Assuntos
Cério/química , Cetotifeno/análise , Luminescência , Compostos Organometálicos/química , Fenantrolinas/química , Produção Agrícola , Cinética , Medições Luminescentes/instrumentação , Estrutura Molecular , Tamanho da Partícula , Propriedades de Superfície
2.
Acta Chim Slov ; 58(3): 563-8, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24062117

RESUMO

A new method using flow injection analysis (FIA) and chemiluminescence (CL) detection has been developed for the rapid, simple and precise determination of pilocarpine hydrochloride (PH). The method is based on the CL reaction of PH with tris(1, 10 phenanthroline)ruthenium(II), [Ru(phen)32+], and Ce(IV) in sulfuric acid medium. Effects of chemical variables were investigated using a central composite design (CCD) and the response surface methodology (RSM). Under optimum conditions, the CL intensity was proportional to the concentration of the drug in solution over the range 0.12-40.00 µg mL-1. The limit of detection (S/N = 3) was 34 ng mL-1. The method was applied successfully to the determination of PH in pharmaceutical formulations and spiked human serum. The relative standard deviation for determination of 7 replicates at a level of 1.5 µg mL-1 of PH was 0.6%. The minimum sampling rate was 70 samples per hour.

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