Determination of amlodipine using terbium-sensitized luminescence in the presence of europium(III) as a co-luminescence reagent

被引:9
|
作者
Al-Kindy, Salma M. Z. [1 ]
Al-Snedi, Abdalla [1 ]
Suliman, Fakhr Eldin O. [1 ]
Al-Lawati, Haidar A. J. [1 ]
机构
[1] Sultan Qaboos Univ, Coll Sci, Dept Chem, Al Khoud 123, Oman
关键词
sensitized luminescence; amlodipine; plasma; pharmaceutical products; co-luminescence; PHARMACEUTICAL FORMULATIONS; BLOOD-PRESSURE; HUMAN PLASMA; BESYLATE; TABLETS; FLUORESCENCE; ATORVASTATIN; VALIDATION; PIROXICAM; SAMPLES;
D O I
10.1002/bio.2602
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive time-resolved luminescence method for the determination of amlodipine (AM) in methanol and in aqueous solution is described. The method is based on the luminescence sensitization of terbium (Tb3+) by formation of a ternary complex with AM in the presence of tri-n-octylphosphine oxide (TOPO) as co-ligand, dodecylbenzenesulfate as surfactant and europium ion as a co-luminescence reagent. The signal for Tb-AM-TOPO is monitored at (ex)=242 nm and (em)=550 nm. Optimum conditions for the formation of the complex in aqueous system were 0.015 m Tris (hydroxylmethyl) amino methane buffer, pH 9.0, TOPO (1.0x10(-4) m), Eu3+ (2.0x10(-7) m), dodecylbenzenesulfate (0.14%) and 6.0x10(-5) m of Tb3+, which allows the determination of 10-50 ppb of AM with a limit of detection of 1.2 ppb. The relative standard deviations of the method range between 0.1 and 0.2% indicated excellent reproducibility of the method. The proposed method was successfully applied for the assay of AM in pharmaceutical formulations and in plasma samples. Average recoveries of 98.5 +/- 0.2% and 95.2 +/- 0.2% were obtained for AM in tablet and plasma samples respectively. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:657 / 662
页数:6
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