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作 者:李放[1] 蔡梅[1] 陈蓓[1] 刘华良[1] 朱峰[1]
出 处:《分析试验室》2016年第9期1012-1015,共4页Chinese Journal of Analysis Laboratory
基 金:江苏科技厅科技支撑计划项目(BE2010745);江苏省"十二五"科教兴卫工程项目(ZX201109)资助
摘 要:依据γ-氨基丁酸(GABA)与茚三酮反应生成蓝紫色化合物,采用氨基酸自动分析仪测定,建立了保健食品中GABA的测定方法。经过对前处理条件的选择和优化,确定保健食品用0.02 mol/L HCl超声提取,用Na OH溶液调节p H至5.5,以柠檬酸盐缓冲溶液为流动相,茚三酮溶液显色,测定波长为570 nm,外标法定量,在0.5~50 mg/L范围内线性关系良好(r=0.9999),方法检出限为0.2 mg/L,定量限为0.5 mg/L。分别在5,10和30 mg/L 3个水平进行加标和精密度实验(n=6),回收率分别为99.2%,93.9%,94.7%,相对标准偏差分别为在5.5%,9.6%,2.2%。方法适合于保健食品中γ-氨基丁酸的定量分析。A method for determination of γ-aminobutyric acid(GABA) in health food was established by automatic amino acid analyzer,which was used to detect a blue violet product formed by the reaction between GABA and ninhydrin. Through the selection and optimization of pretreatment conditions,the results showed that the optimum condition for extraction was as follow: the health foods were extrac ted by ultrasonic using 0. 02 mol/L hydrochloric acid as extraction solvent,sodium hydroxide solution was used to adjust p H to 5. 5,the citrate buffer solution was used as the mobile phase,ninhydrin was used as chromogenic agent,the detection wavelength was 570 nm,and the external standard method was used for quantification. GABA had a good linear relationship in the range of0. 5 ~ 50 mg/L with correlation coefficient(r) of 0. 9999. The limit of detection was 0. 2 mg/L,and the limit of quantitation was 0. 5 mg/L. The recoveries were 99. 2%,93. 9% and 94. 7%(n = 6) respectively at the spiked levels of 5,10 and 30 mg/L,and the relative standard deviations were 5. 5%,9. 6% and 2. 2%. The method is suitable for the quantitative analysis of γ-aminobutyric acid in health food.
关 键 词:γ-氨基丁酸(GABA) 保健食品 氨基酸自动分析仪
分 类 号:TS218[轻工技术与工程—粮食、油脂及植物蛋白工程]
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