Development of liquid chromatography-mass spectrometry method to determine biotin content in nutritional products and supplements

Trang Luu Thi Huyen, Le Vu Thi Nhat, Trang Vu Thi, Hao Le Thi Hong
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引用次数: 1

Abstract

The study was carried out to develop a method for determining the biotin content in nutritional products and supplements by liquid chromatography-mass spectrometry (LC-MS/ MS) combined with a fast and simple pretreatment. The analyzed sample was hydrolyzed in acetate buffer (50 mM, pH 4) with the presence of ascorbate solution (10%) at 120 ± 1°C. After adding the internal standard (2H4-biotin), the mixture was analyzed on LC-MS/ MS system using C18 (100 mm × 2.1 mm; 1.7 µm) column and 0.1% formic acid and MeOH as mobile phases. The analyte was detected on an MS/MS system with an ESI (+) ionization source. The method was validated following the AOAC criteria. The method detection limit was 0.15 - 4.20 µg/100g, the method quantitative limit was in the range of 0.5 - 14.0 µg/100g, the recovery range was 81.3 - 107.3%, the repeatability was in the range of 2.00 - 7.30 %, the reproducibility was 2.50 - 7.70%, which were in accordance with AOAC requirements. The method has been applied to analyze biotin content in 10 nutritional products and 10 supplements purchased in the market.
液相色谱-质谱法测定营养品和保健品中生物素含量的研究
建立了一种快速、简便的前处理相结合的液相色谱-质谱联用法测定营养品和保健品中生物素含量的方法。所分析的样品在醋酸缓冲液(50 mM, pH 4)中水解,抗坏血酸溶液(10%)存在,温度为120±1℃。加入内标物(2h4 -生物素)后,采用C18 (100 mm × 2.1 mm;1.7µm)色谱柱,流动相为0.1%甲酸和甲醇。分析物在ESI(+)电离源的MS/MS系统上检测。按照AOAC标准对方法进行了验证。方法检出限为0.15 ~ 4.20µg/100g,定量限为0.5 ~ 14.0µg/100g,加样回收率为81.3 ~ 107.3%,重复性为2.00 ~ 7.30%,重现性为2.50 ~ 7.70%,符合AOAC要求。该方法已应用于市场上购买的10种营养品和10种补品的生物素含量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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