Method for simultaneous analysis of eight vitamin E isomers in various foods by high performance liquid chromatography and fluorescence detection

• Published in: Journal of Chromatography A 2011-11, Vol.1218 (47), p.8496-8502
• Main Authors: Pinheiro-Sant’Ana, Helena Maria, Guinazi, Michele, Oliveira, Daniela da Silva, Della Lucia, Ceres Mattos, Reis, Bárbara de Lazzari, Brandão, Sebastião César Cardoso
• Format: Article
• Language: English
• Subjects: acetates; Biological and medical sciences; canola; cis-trans isomers; detection limit; Eggs; flour; fluorescence; Food industries; Fundamental and applied biological sciences. Psychology; General aspects; herbs; high performance liquid chromatography; linseed; Methods of analysis, processing and quality control, regulation, standards; olives; saponification; Seeds; solvents; soybeans; spices; Tocopherols; Tocotrienols; vegetable oil; Vegetable oils; Vegetables
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2011.09.067

► Our optimized methods for analysis of vitamin E isomers in the foods were efficient. ► Detection of eight vitamin E isomers was performed in only two runs and short times. ► Direct extraction used for tocopherols and tocotrienols in foods was simple and fast. ► Direct extraction preserved vitamin E isomers when compared to saponification. The objective of this study was to optimize a method to investigate the occurrence and to quantify the full isomeric composition of vitamin E (α-, β-, γ- and δ-tocopherols and tocotrienols) in 6 vegetables (raw and cooked), 3 herbs/spices, raw and cooked eggs, vegetable oils (canola, olive and soybean), flaxseed and sorghum (flour and seeds) and soy (flour) by HPLC with fluorescence detection. Different conditions of extraction and analysis were tested. The optimized method consisted of direct extraction with solvent (hexane:ethyl acetate, 85:15, v/v). For analysis normal phase column was used with mobile phase consisting of hexane:isopropanol:acetic acid (98.9:0.6:0.5) with isocratic elution and fluorescence detection. Excellent separation of all isomers was obtained along with adequate quantification in the foods analyzed. Recovery rates of standards ranged from 91.3 to 99.4%. The linearity range for each isomer varied from 2.5 to 137.5 ng/mL ( R 2 greater than 0.995 in all cases). Detection limits ranged from 21.0 to 48.0 ng/mL for tocopherols and from 56.0 to 67.0 ng/mL for tocotrienols, while quantification limits ranged from 105.0 to 240.0 ng/mL for tocopherols and from 280.0 to 335.0 ng/mL for tocotrienols. The optimized method was considered simple, fast and reliable, and also preserved vitamin E isomers when compared to validated methods involving saponification.