Electrochemical behavior and electrochemical determination of carbamazepine at an ionic liquid modified carbon paste electrode in the presence of sodium dodecyl sulfate

被引:27
作者
Liu, Li-Hong [1 ,2 ]
Duan, Cheng-Qian [1 ,3 ]
Gao, Zuo-Ning [1 ]
机构
[1] Ningxia Univ, Coll Chem & Chem Engn, Key Lab Energy Sources & Chem Engn, Yinchuan 750021, Peoples R China
[2] Heihe Coll, Dept Chem, Heihe 164300, Peoples R China
[3] Ningxia Med Univ, Higher Vocat Coll, Yinchuan 750004, Peoples R China
关键词
carbamazepine; sodium dodecyl sulfate; ionic liquid modified carbon paste electrode; electrochemistry; ELECTROCATALYTIC OXIDATION; VOLTAMMETRIC DETERMINATION; SELECTIVE DETERMINATION; ASCORBIC-ACID; URIC-ACID; CHROMATOGRAPHY; DOPAMINE; SURFACTANTS; METABOLITES; HEMOGLOBIN;
D O I
10.2298/JSC110420188L
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical behavior and electrochemical determination of carbamazepine (CBZ) at a hydrophobic ionic liquid 1-benzyl-3-methylimidazole hexafluorophosphate ([BnMIM]PF6) modified carbon paste electrode ([BnMIM]PF6/CPE) in the presence of sodium dodecyl sulfate (SDS) were investigated. A well-defined and sensitive oxidation peak was observed at the [BnMIM]PF6/CPE in the presence of SDS and a 0.10 M phosphate buffer solution (pH 6.80). The oxidation peak current of CBZ increased significantly at the [BnMIM]PF6/CPE in the presence of SDS compared with that in the absence of SDS at the carbon paste electrode. It suggested that both SDS and [BnMIM]PF6/CPE show an obvious enhancing effect on the electrochemical oxidation of CBZ. The electrochemical kinetic parameters for CBZ at the [BnMIM]PF6/CPE in aqueous SDS solutions were also determined by chronocoulometry and chronoamperometry. Finally, the experimental conditions were optimized, and a new electrochemical method for the determination for CBZ was established. The oxidation peak current was linearly dependent on the CBZ concentration in the range 7.0 mu M to 0.7 mM, with a detection limit of 0.98 mu M (signal to noise ratio, S/N = 3). The relative standard deviation for six determinations of 0.10 mM CBZ was between 1.40 and 2.13 %. The proposed method was applied in the determination of CBZ in commercial tablet samples.
引用
收藏
页码:483 / 496
页数:14
相关论文
共 56 条
[1]   Electrochemical Behaviour of Carbamazepine in Acetonitrile and Dimethylformamide Using Glassy Carbon Electrodes and Microelectrodes [J].
Atkins, S. ;
Sevilla, J. M. ;
Blazquez, M. ;
Pineda, T. ;
Gonzalez-Rodriguez, J. .
ELECTROANALYSIS, 2010, 22 (24) :2961-2966
[2]  
BARD AJ, 1980, ELECTROCHEMICAL METH, P200
[3]   Dose-dependent metabolism of carbamazepine in humans [J].
Bernus, I ;
Dickinson, RG ;
Hooper, WD ;
Eadie, MJ .
EPILEPSY RESEARCH, 1996, 24 (03) :163-172
[4]   Liquid chromatography-electrospray mass spectrometry determination of carbamazepine, oxcarbazepine and eight of their metabolites in human plasma [J].
Breton, H ;
Cociglio, M ;
Bressolle, F ;
Peyriere, H ;
Blayac, JP ;
Hillaire-Buys, D .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 828 (1-2) :80-90
[5]   Concentration-dependent diffusion in room temperature ionic liquids: a microelectrode study [J].
Brooks, CA ;
Doherty, AP .
ELECTROCHEMISTRY COMMUNICATIONS, 2004, 6 (08) :867-871
[6]   DETERMINATION OF ANTIEPILEPTIC DRUGS [J].
BURKE, JT ;
THENOT, JP .
JOURNAL OF CHROMATOGRAPHY, 1985, 340 (MAY) :199-241
[7]   DETERMINATION OF STANDARD POTENTIALS AND ELECTRON-TRANSFER RATES FOR HALOBIPHENYLS FROM ELECTROCATALYTIC DATA [J].
CONNORS, TF ;
RUSLING, JF ;
OWLIA, A .
ANALYTICAL CHEMISTRY, 1985, 57 (01) :170-174
[8]  
DUNNBIER U, 1986, PHARMAZIE, V41, P567
[9]   The analysis of a group of acidic pharmaceuticals, carbamazepine, and potential endocrine disrupting compounds in wastewater irrigated soils by gas chromatography-mass spectrometry [J].
Duran-Alvarez, Juan C. ;
Becerril-Bravo, Elias ;
Silva Castro, Vanessa ;
Jimenez, Blanca ;
Gibson, Richard .
TALANTA, 2009, 78 (03) :1159-1166
[10]   Ionic liquids as electrolytes [J].
Galinski, Maciej ;
Lewandowski, Andrzej ;
Stepniak, Izabela .
ELECTROCHIMICA ACTA, 2006, 51 (26) :5567-5580