Sensitive ergotamine determination in pharmaceuticals and biological samples using cloud point preconcentration and spectrofluorimetric detection

被引:9
作者
Wang, Chien C. [1 ]
Fernandez, Liliana P. [1 ,2 ]
Roxana Gomez, Maria [1 ,2 ,3 ]
机构
[1] INQUISAL CONICET, San Luis, Argentina
[2] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Area Quim Analit, San Luis, Argentina
[3] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Dept Farm, San Luis, Argentina
关键词
Ergotamine; Cloud point extraction; Spectrofluorimetry; Pharmaceuticals; Urine; Saliva; COMBINED METHODOLOGY; MEDIATED SEPARATION; EXTRACTION; ALKALOIDS; CHROMATOGRAPHY; TARTRATE;
D O I
10.1016/j.aca.2013.01.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new cloud point extraction (CPE) method for ergotamine analysis using fluorimetric detection is described. Ergotamine from an aqueous solution was preconcentrated into a smaller surfactant-rich phase using nonionic surfactant polyoxyethylene(7.5)nonylphenylether (PONPE 7.5). Differently from the conventional CPE procedure in which the resulting surfactant-rich phase is diluted by a fluidificant before its analysis, in this method the fluorescence measurements were carried out directly onto the undiluted surfactant-rich phase. The high viscosity provided by the undiluted surfactant rich phase greatly improved the fluorescence emission of ergotamine, leading to a total enhancement factor of 1325. This spectral advantage plus the preconcentration factor achieved, contributed to the method sensitivity allowing the ergotamine determination at trace level concentration. Under optimal experimental conditions, a linear calibration curve was obtained from 3.81 x 10(-7) to 1.10 mu g mL(-1), with detection and quantification limits of 0.11 and 0.38 pg mL(-1), respectively. The accuracy and versatility of the present methodology were proved by analyzing ergotamine in real samples of different natures such as pharmaceuticals, urine and saliva. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:90 / 95
页数:6
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