Imipramine sensing in pharmaceutical formulations using boron-doped diamond electrode

被引:19
作者
Oliveira, Sameque N. [1 ]
Ribeiro, Francisco W. P. [2 ]
Sousa, Camila P. [1 ]
Soares, Janete Eliza S. [3 ]
Suffredini, Hugo B. [4 ]
Becker, Helena [1 ]
de Lima-Neto, Pedro [1 ]
Correia, Adriana N. [1 ]
机构
[1] Univ Fed Ceara, Ctr Ciencias, Dept Quim Analit & Fis Quim, Bloco 940,Campus Pici, BR-60455970 Fortaleza, Ceara, Brazil
[2] Univ Fed Cariri, Inst Formacao Educadores, Rua Olegario Emidio Aradjo,S-N, BR-63260000 Brejo Santo, CE, Brazil
[3] Univ Fed Ceara, Fac Farm Odontol & Enfermagem, Dept Farm, Rua Capitao Francisco Pedro 1210, BR-60430370 Fortaleza, Ceara, Brazil
[4] Univ Fed ABC, Ctr Ciencias Nat & Humanas, R Abolicdo,S-N,Bloco B, BR-09210170 Santo Andre, SP, Brazil
关键词
Imipramine; Boron-doped diamond electrode; Square-wave voltammetry; PERFORMANCE LIQUID-CHROMATOGRAPHY; CARBON-PASTE ELECTRODE; STRIPPING VOLTAMMETRIC DETERMINATION; TRICYCLIC ANTIDEPRESSANT DRUGS; ELECTROANALYTICAL DETERMINATION; SPECTROPHOTOMETRIC DETERMINATION; SPECTROFLUOROMETRIC METHOD; ELECTROCHEMICAL OXIDATION; SENSITIVE DETERMINATION; ULTRAVIOLET DETECTION;
D O I
10.1016/j.jelechem.2017.01.067
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper describes the development of an electroanalytical procedure proposal for the determination of tricyclic antidepressant imipramine (IMP) in commercial pharmaceutical formulations using boron-doped diamond electrode and square-wave voltammetry. The electrochemical oxidation of imipramine was studied in 0.04 mol L-1 Britton-Robinson buffer solution. The voltammetric results showed two well-defined oxidation peaks with potentials of 0.04 V and 0.82 V vs. Ag/AgCl/3 mol L-1 Cl- for peaks 1 and 2, respectively. The effect of the experimental and voltammetric parameters was evaluated and the best performance was obtained in pH 7.4, pulses application frequency of potential of 100 Hz, amplitude of 50 mV and potential increment of 2 my. Under these conditions, the analytical curves were obtained in the linear range of concentration from 1.73 x 10(-7) mol L-1 to 2.53 x 10(-6) mol L-1 (r = 0.9984), with detection and quantitation limits 435 x 10(-8) mol L-1 and 1.45 x 10(-7) mol L-1, respectively. The proposed method was applied with success in the determination of IMP in commercial pharmaceutical formulations and validated by comparison with standard method for determination of imipramine. The obtained results were in close agreement, at a 95% confidence level, with those obtained using an official method of the British Pharmacopeia. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 124
页数:7
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