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采用反相液相色谱法测定补充剂和原料中番茄红素的方法:单实验室验证

Method for the determination of lycopene in supplements and raw material by reversed-phase liquid chromatography: single-laboratory validation.

作者信息

Miller André, Pietsch Bernd, Faccin Nicole, Schierle Joseph, Waysek Edward H

机构信息

DSM Nutritional Products Ltd, Research and Development, Analytical Research Center, PO Box 2676, CH-4002 Basel, Switzerland.

出版信息

J AOAC Int. 2008 Nov-Dec;91(6):1284-97.

Abstract

A single-laboratory validation study was conducted for a liquid chromatographic (LC) method for the determination of total and all-trans-lycopene in a variety of dietary supplements and raw materials. Gelatin-based and other water-dispersible beadlets, or tablets, capsules, and softgels containing such product forms, were digested with protease. Alginate formulations and the respective applications were treated with an alkaline sodium EDTA acetate buffer to release lycopene from the matrix. Lycopene and other carotenoids were extracted from the resulting aqueous suspensions with dichloromethane and ethanol. Oily product forms were directly dissolved in dichloromethane and ethanol. The extracts were chromatographed on an isocratic high-performance LC system using a C16 alkylamide modified silica column that provided satisfactory resolution of all-trans-lycopene from its predominant cis-isomers and separated the lycopene isomers from other carotenoids such as alpha- and beta-carotene, cryptoxanthin, lutein, and zeaxanthin. The within-day precision relative standard deviation (RSD) for the determination of total lycopene ranged from 0.9 to 5.7% over concentration ranges of 50-200 g/kg for raw materials and 0.3-24 g/kg for dietary supplements. The intermediate precision RSD (total RSD) ranged from 0.8 to 8.9%. Recoveries obtained for beadlet and tablet material for the different extraction variants ranged from 95.0 to 102.1% at levels of 0.02-20 g/kg for tablets and from 95.0 to 101.1% at levels of 1-200 g/kg for beadlet material.

摘要

针对一种液相色谱(LC)方法开展了单实验室验证研究,该方法用于测定多种膳食补充剂和原材料中的总番茄红素及全反式番茄红素。以明胶为基质的及其他水分散性小丸剂,或含有此类产品形式的片剂、胶囊和软胶囊,用蛋白酶进行消化。藻酸盐制剂及其相应应用用碱性乙酸钠乙二胺四乙酸缓冲液处理,以从基质中释放番茄红素。用二氯甲烷和乙醇从所得水悬浮液中提取番茄红素和其他类胡萝卜素。油性产品形式直接溶于二氯甲烷和乙醇。提取物在等度高效液相色谱系统上进行色谱分析,使用C16烷基酰胺改性硅胶柱,该柱能使全反式番茄红素与其主要顺式异构体得到令人满意的分离,并将番茄红素异构体与其他类胡萝卜素(如α-和β-胡萝卜素、隐黄质、叶黄素和玉米黄质)分离。在原材料浓度范围为50 - 200 μg/kg以及膳食补充剂浓度范围为0.3 - 24 μg/kg时,日内精密度相对标准偏差(RSD)测定总番茄红素的范围为0.9%至5.7%。中间精密度RSD(总RSD)范围为0.8%至8.9%。对于不同提取变体的小丸剂和片剂材料,在片剂水平为0.02 - 20 μg/kg时回收率范围为95.0%至102.1%,在小丸剂材料水平为1 - 200 μg/kg时回收率范围为95.0%至101.1%。

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