引用本文:
Ya Shan HAN, Yun Qing DAI. SIMULTANEOUS DETERMINATION OF FAT SOLUBLE VITAMINS A, D3, E AND K1 IN FORTIFIED MILK POWDERS BY HPLC[J]. Chinese Chemical Letters,
1991, 3(8): 649-652.
Citation: Ya Shan HAN, Yun Qing DAI. SIMULTANEOUS DETERMINATION OF FAT SOLUBLE VITAMINS A, D3, E AND K1 IN FORTIFIED MILK POWDERS BY HPLC[J]. Chinese Chemical Letters, 1991, 3(8): 649-652.
Citation: Ya Shan HAN, Yun Qing DAI. SIMULTANEOUS DETERMINATION OF FAT SOLUBLE VITAMINS A, D3, E AND K1 IN FORTIFIED MILK POWDERS BY HPLC[J]. Chinese Chemical Letters, 1991, 3(8): 649-652.
SIMULTANEOUS DETERMINATION OF FAT SOLUBLE VITAMINS A, D3, E AND K1 IN FORTIFIED MILK POWDERS BY HPLC
摘要:
A high performance liquid chromatographic method for the simultaneous determination of four fat soluble vitamins: retinol (vitamin A), cholecalciferol(vitamin D), tocopherol(vitamin E) and phylloquinone(vitamin K1) in fortified milk powders and egg yolk has been developed. The method requires enzymatic hydrolysis of lipid component of the sample as a pretreatment. Several factors which influence the enzymatic hydrolysis were studied-Separation was achieved using μ-Bondapak C-18 column(3.9×300mm), 98% methanol as mobile phase, a double channel detection was selected; vitamins D3 E1 K1 were detected by UV spectrophotometry (265 nm) first, then vitamin A by fluorometry (EX 325nm, EM 480nm). The retention times of vitamin A1 D3, E and K1 4.87, 9.00, 10.58 and 15.45 min respectively. Detection limit were 0.64, 0.25, 0.50 and 0.07 ng; and the recoveries were 90.5%~103.6%, 90.0%~95.6%, 91.7%~98.8%, 91.5%~98.6%, respectively. The vitamins A, D3, E, K1 contents in foods were determined satisfactorily.
English
SIMULTANEOUS DETERMINATION OF FAT SOLUBLE VITAMINS A, D3, E AND K1 IN FORTIFIED MILK POWDERS BY HPLC
Abstract:
A high performance liquid chromatographic method for the simultaneous determination of four fat soluble vitamins: retinol (vitamin A), cholecalciferol(vitamin D), tocopherol(vitamin E) and phylloquinone(vitamin K1) in fortified milk powders and egg yolk has been developed. The method requires enzymatic hydrolysis of lipid component of the sample as a pretreatment. Several factors which influence the enzymatic hydrolysis were studied-Separation was achieved using μ-Bondapak C-18 column(3.9×300mm), 98% methanol as mobile phase, a double channel detection was selected; vitamins D3 E1 K1 were detected by UV spectrophotometry (265 nm) first, then vitamin A by fluorometry (EX 325nm, EM 480nm). The retention times of vitamin A1 D3, E and K1 4.87, 9.00, 10.58 and 15.45 min respectively. Detection limit were 0.64, 0.25, 0.50 and 0.07 ng; and the recoveries were 90.5%~103.6%, 90.0%~95.6%, 91.7%~98.8%, 91.5%~98.6%, respectively. The vitamins A, D3, E, K1 contents in foods were determined satisfactorily.
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