Comparative performances of a bare graphite-polyurethane composite electrode unmodified and modified with graphene and carbon nanotubes in the electrochemical determination of escitalopram

被引:35
作者
Baccarin, Marina [1 ]
Cervini, Priscila [1 ]
Gomes Cavalheiro, Eder Tadeu [1 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13566590 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Escitalopram; Graphite-polyurethane composite electrode; Graphene; Carbon nanotubes; Antidepressant determination; TABLET DOSAGE FORM; PHARMACEUTICAL FORMULATIONS; SPECTROPHOTOMETRIC DETERMINATION; CAPILLARY-ELECTROPHORESIS; VOLTAMMETRIC SENSOR; BIOLOGICAL-FLUIDS; OXALATE; CITALOPRAM; CLONAZEPAM; ELECTROOXIDATION;
D O I
10.1016/j.talanta.2017.08.094
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A bare composite graphite-polyurethane electrode (EGPU) and two other modified with graphene (EGPU-GR) and functionalized multi-walled carbon nanotubes (EGPU-CNTs) were prepared and compared regarding their voltammetric response to escitalopran (EST). The modifiers were characterized by Raman spectroscopy and the resulting electrode materials by contact angle measurements with a hydrophilicity character in the ascending order for the composites: GPU > GPU-GR > GPU-CNTs and scanning electron microscopy (SEM). The electroactive areas of the EGPU, EGPU-GR, and EGPU-CNTs were 0.065, 0.080, and 0.092 cm(2), respectively, calculated from the chronocoulometry using K-3[Fe(CN)(6)] as a probe and the Cottrell equation. The cyclic voltammograms obtained for EST indicated irreversible electrochemical behavior, with an anodic peak at cu. + 0.80 V (vs. SCE). These measurements were carried out with the three electrodes, and comparison of the analytical responses led to the EGPU-GR electrode being selected for use in the subsequent experiments. Under optimal conditions, square wave and differential pulse voltammetry at EGPU-GR presented linear dynamic ranges between 1.5 x 10(-6) and 1.2 x 10(-5) mol L-1, with a detection limit of 2.5 x 10(-7) mol L-1 (SWV) and 1.5 x 10(-6) and 1.2 x 10(-5) mol L-1, with a detection limit of 3.2 x 10(-7) mol L-1 (DPV) for EST. The proposed method was applied for the quantification of EST in synthetic urine and cerebrospinal fluid samples, offering advantages including simplicity of fabrication, no requirement for analyte preconcentration and surface renewal, fast response, and selectivity.
引用
收藏
页码:1024 / 1032
页数:9
相关论文
共 52 条
[1]  
Ajayan PM, 2001, TOP APPL PHYS, V80, P391
[2]  
Al-Amri FMG, 2013, INT J ELECTROCHEM SC, V8, P10044
[3]  
Al-Tamimi SA, 2013, J INDIAN CHEM SOC, V90, P309
[4]  
Al-Tamimi SA, 2012, ASIAN J CHEM, V24, P5515
[5]   Flow-injection chemiluminescence and electrogenerated chemiluminescence determination of escitalopram oxalate in tablet form [J].
Alarfaj, Nawal A. ;
Aly, Fatma A. ;
Al-Qahtany, Abeer A. .
LUMINESCENCE, 2013, 28 (01) :84-92
[6]  
Annamalai C., 2011, J BIOSCI RES, V2, P142
[7]   Comparative study of first- and second-order Raman spectra of MWCNT at visible and infrared laser excitation [J].
Antunes, E. F. ;
Lobo, A. O. ;
Corat, E. J. ;
Trava-Airoldi, V. J. ;
Martin, A. A. ;
Verissimo, C. .
CARBON, 2006, 44 (11) :2202-2211
[8]   Electrocatalysis at graphite and carbon nanotube modified electrodes: edge-plane sites and tube ends are the reactive sites [J].
Banks, CE ;
Davies, TJ ;
Wildgoose, GG ;
Compton, RG .
CHEMICAL COMMUNICATIONS, 2005, (07) :829-841
[9]  
Bard A.J, 2002, Student Solutions Manual to accompany Electrochemical Methods: Fundamentals and Applicaitons, V2e
[10]   Determination of paracetamol at a graphite-polyurethane composite electrode as an amperometric flow detector [J].
Cervini, Priscila ;
Gomes Cavalheiro, Eder Tadeu .
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2008, 19 (05) :836-841