A high-throughput liquid chromatography tandem mass spectrometry method for the comparative determination of fluticasone propionate by reversed-phase liquid chromatography and capillary electrophoresis methods in pharmaceutical nasal sprays

被引:8
|
作者
Sangoi, Maximiliano da Silva [1 ]
Wrasse, Micheli [2 ]
D'Avila, Felipe Bianchini [2 ]
Bernardi, Raquel Martini [1 ]
de Oliveira, Paulo Renato [3 ]
Dalmora, Sergio Luiz [2 ]
Bueno Rolim, Clarice Madalena [2 ]
机构
[1] Univ Fed Rio Grande do Sul, Fac Pharm, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Fed Santa Maria, Dept Ind Pharm, BR-97105900 Santa Maria, RS, Brazil
[3] Univ Fed Santa Catarina, Dept Pharmaceut Sci, BR-88040900 Florianopolis, SC, Brazil
关键词
fluticasone propionate; tandem mass spectrometry; liquid chromatography; capillary electrophoresis; validation; ANALYTICAL METHOD VALIDATION; LC-MS/MS METHOD; HUMAN PLASMA; ALLERGIC RHINITIS; CORTICOSTEROIDS; QUANTIFICATION; FORMULATIONS; INTRANASAL; EXTRACTION; ASTHMA;
D O I
10.1255/ejms.1044
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
A simple, specific, rapid and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the analysis of fluticasone propionate (FP) in pharmaceutical formulations was developed and validated using deflazacort as internal standard (IS). The LC-MS/MS method was carried out on a C(8) column (50 mm) with a mobile phase consisted of methanol:water (95:5, v/v)-100 mM formic acid-50 mM ammonium acetate (90:5:5,v/v/v). The mass spectrometry method was performed employing positive atmospheric pressure chemical ionization technique, operating in multiple reaction monitoring mode. The chromatographic separation was obtained within 1.5 min and it was linear in the concentration range of 10-1000 ng mL(-1). Moreover, method validation demonstrates acceptable results for the specificity, accuracy, precision and robustness. The proposed method was successfully applied for the quantitative analysis of FP nasal sprays and the results were compared to validated liquid chromatography and capillary electrophoresis methods with photodiode array detectors showing non-significant difference (P > 0.05).
引用
收藏
页码:723 / 730
页数:8
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