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出 处:《药物分析杂志》2014年第2期306-309,共4页Chinese Journal of Pharmaceutical Analysis
基 金:陕西省社会科学基金项目(13G020)
摘 要:目的:建立保健食品中5-羟甲基糠醛(5-hydroxymethyl furfural,5-HMF)快速筛查定性定量分析方法。方法:样品经色谱甲醇提取富集,气相色谱-质谱联用(GC-MS),Scan模式进行定性,SIM选择离子扫描模式进行定量检测。采用DB-5 ms毛细管色谱柱(30 m×0.25 mm×0.25 μm),程序升温:初始温度70 ℃(保持2 min),8 ℃·min^-1升至100 ℃,再以6 ℃·min^-1升至125 ℃(保持3 min),再以25 ℃·min^-1升至280 ℃(保持2 min);选择EI离子源,溶剂延迟2 min,质谱扫描范围50-600 amu。结果:5-羟甲基糠醛在2.050-102.5 μg·mL^-1范围内均呈良好的线性关系,相关系数为0.9995;检出限(S/N=3)为0.02 μg·mL^-1 ,加标回收率为84.0%-96.5%;样品筛查结果发现7批含糖口服液中检测出5-羟甲基糠醛。结论:该法简便、快速、准确,专属性强,可用于保健食品质量控制中检测5-羟甲基糠醛的残留量。Objective: To develop a qualitative and quantitative analytical method for rapid screening of 5-hydroxymethyl furfural (5-HMF) in health food. Methods: Methanol solvent extraction was used to get the enrichment of samples.Qualitative analysis was carried out by GC-MS and scan mode,quantitative detection was performed by selected ion monitoring (SIM) mode.The analytical capillary column was DB-5 ms (30 m×0.2 5 mm×0.25 μm).The oven temperature was set at 70 ℃ (maintained for 2 min) initially,which was programmed to rise up to 100 ℃ by 8 ℃·min^-1,then rise up to 125 ℃(maintained for 3 min) by 6 ℃·min^-1,then rise up to 280 ℃(maintained for 2 min) by 25 ℃·min^-1.The EI ion source was adopted,and the solvent was delayed for 2 min.The MS scanning range was 50-600 amu. Results: The method showed good linearity within the range of 2.050-102.5 μg·mL^-1 (r〉 0.9995) for 5-HMF.The limit of detection was 0.02 μg·mL^-1(S/N=3).The recoveries were 84.0%-96.5%.5-hydroxymethyl furfural was identified in seven batch samples of sugar-containing oral liquid. Conclusion: This method is convenient,fast,accurate and highly selective,which is suitable for the determination of 5-HMF residue in health food.
关 键 词:气相色谱-质谱 5-羟甲基糠醛残留 快速筛查 保健食品 定性定量
分 类 号:R917[医药卫生—药物分析学]
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