Fast analysis of isoflavones by high-performance liquid chromatography using a column packed with fused-core particles

The recent development of fused-core technology in HPLC columns is enabling faster and highly efficient separations. This technology was evaluated for the development of an fast analysis method for the most relevant soy isoflavones. A step-by-step strategy was used to optimize temperature (25-50 °C), flow rate (1.2-2.7 mL/min), mobile phase composition and equilibration time (1-5 min). Optimized conditions provided a method for the separation of all isoflavones in less than 5.8 min and total analysis time (sample-to-sample) of 11.5 min. Evaluation of chromatographic performance revealed excellent reproducibility, resolution, selectivity, peak symmetry and low limits of detection and quantification levels. The use of a fused-core column allows highly efficient, sensitive, accurate and reproducible determination of isoflavones with an outstanding sample throughout and resolution. The developed method was validated with different soy samples with a total isoflavone concentration ranging from 1941.53 to 2460.84 μg g-1 with the predominant isoflavones being isoflavone glucosides and malonyl derivatives. © 2010 Elsevier B.V.

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Bibliographic Details
Main Authors: Manchón, N., D'Arrigo, M., García Lafuente, Ana María, Guillamón Fernández, Eva, Villares, A., Ramos, A., Martínez, J. A., Rostagno, M. A.
Format: artículo biblioteca
Language:English
Published: Elsevier 2010
Subjects:Soybeans, Isoflavones, High-performance liquid chromatography, Fused-core, Fast analysis,
Online Access:http://hdl.handle.net/20.500.12792/2599
http://hdl.handle.net/10261/290093
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Summary:The recent development of fused-core technology in HPLC columns is enabling faster and highly efficient separations. This technology was evaluated for the development of an fast analysis method for the most relevant soy isoflavones. A step-by-step strategy was used to optimize temperature (25-50 °C), flow rate (1.2-2.7 mL/min), mobile phase composition and equilibration time (1-5 min). Optimized conditions provided a method for the separation of all isoflavones in less than 5.8 min and total analysis time (sample-to-sample) of 11.5 min. Evaluation of chromatographic performance revealed excellent reproducibility, resolution, selectivity, peak symmetry and low limits of detection and quantification levels. The use of a fused-core column allows highly efficient, sensitive, accurate and reproducible determination of isoflavones with an outstanding sample throughout and resolution. The developed method was validated with different soy samples with a total isoflavone concentration ranging from 1941.53 to 2460.84 μg g-1 with the predominant isoflavones being isoflavone glucosides and malonyl derivatives. © 2010 Elsevier B.V.