Trace determination of vardenafil hydrochloride in commercial formulation and human serum by adsorptive anodic stripping voltammetry at a carbon paste electrode
被引:18
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作者:
Ghoneim, Mohamed M.
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机构:
Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, EgyptTanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
Ghoneim, Mohamed M.
[1
]
Hassanein, Amera M.
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机构:
Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, EgyptTanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
Hassanein, Amera M.
[1
]
Salahuddin, Nehal A.
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Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, EgyptTanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
Salahuddin, Nehal A.
[1
]
El-Desoky, Hanaa S.
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Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, EgyptTanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
El-Desoky, Hanaa S.
[1
]
Elfiky, Mona N.
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Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, EgyptTanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
Elfiky, Mona N.
[1
]
机构:
[1] Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
Stripping voltammetry;
Determination;
Formulations;
Human serum;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
PHARMACEUTICAL-PREPARATIONS;
ELECTROCHEMICAL-BEHAVIOR;
HUMAN PLASMA;
SILDENAFIL;
TADALAFIL;
DRUG;
PHENOTHIAZINES;
METABOLITES;
INHIBITOR;
D O I:
10.1007/s10008-013-2020-8
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
The electrochemical behavior of vardenafil HCl (VRL) at a carbon paste electrode (CPE) was investigated by cyclic voltammetry, and the mechanism of its oxidation was suggested and discussed. A simple Nujol-based CPE in combination with a sensitive square-wave adsorption anodic stripping voltammetry method was described for trace determination of VRL. The described method showed excellent performance for trace determination of VRL in its formulation "LevitraA (R) tablets" without interference from excipients. The results were statistically compared with those obtained with an established HPLC method; nonsignificant differences were found between the described voltammetric and HPLC methods. The described stripping voltammetric method is highly sensitive (limit of detection = 3 x 10(-10) mol L-1 and limit of quantitation = 1 x 10(-9) mol L-1). It was successfully applied for the determination of VRL in spiked human serum without the necessity for pretreatment and/or time-consuming extraction steps prior to the analysis.