孙 健,张 甦,胡 青,毛秀红,季 申.柱前衍生-高效液相色谱法测定保健食品中 16种氨基酸的含量[J].食品安全质量检测学报,2016,7(7):2715-2719
柱前衍生-高效液相色谱法测定保健食品中 16种氨基酸的含量
Determination of 16 kinds of amino acids in health foods by high performance liquid chromatography with pre-column derivatization
投稿时间:2016-06-03  修订日期:2016-06-29
DOI:
中文关键词:  保健食品  氨基酸  邻苯二甲醛  9-芴甲基氯甲酸酯  柱前衍生  高效液相色谱法
英文关键词:health food  amino acid  protein  o-Phthalaldehyde  9-fluorenylmethyl chloroformate  pre-column derivatization  high performance liquid chromatography
基金项目:上海市科学技术委员会项目(14DZ2294000,14DZ1900302)
作者单位
孙 健 上海市食品药品检验所 
张 甦 上海市食品药品检验所 
胡 青 上海市食品药品检验所 
毛秀红 上海市食品药品检验所 
季 申 上海市食品药品检验所 
AuthorInstitution
SUN Jian Shanghai Institute for Food and Drug Control 
ZHANG Su Shanghai Institute for Food and Drug Control 
HU Qing Shanghai Institute for Food and Drug Control 
MAO Xiu-Hong Shanghai Institute for Food and Drug Control 
JI Shen Shanghai Institute for Food and Drug Control 
摘要点击次数: 1556
全文下载次数: 1783
中文摘要:
      目的 建立柱前衍生-高效液相色谱法测定保健食品中16种氨基酸的含量。方法 优化GB/T 5009.124-2003的前处理方法, 样品经稀释或置于顶空瓶中直接酸水解; 并采用OPA/FMOC柱前衍生法, 色谱柱为Thermo ODS Hypersil, 以醋酸钠缓冲液(含三乙胺、四氢呋喃)和醋酸钠缓冲液(含乙腈、甲醇)为流动相进行梯度洗脱, 在338 nm和262 nm检测波长下进行高效液相色谱法检测。结果 16种氨基酸在4~250 μg/mL范围内呈现良好线性关系, 在10 μg/mL水平下加标回收率为85.8%~115.2%, RSD为0.1%~9.1%(n=6), 检出限在0.2~4.6 ng范围内。结论 本方法操作简便、灵敏度高, 可应用于实际样品的测定。
英文摘要:
      Objective To establish a method for determination of 16 kinds of amino acids in health foods by high performance liquid chromatography (HPLC) with pre-column derivatization. Methods By optimizing pretreatment and analytical method of GB/T 5009.124-2003, samples were diluted or direct acid hydrolyzed in headspace bottle, and the amino acids were determined by HPLC after pre-column derivatization with o-Phthalaldehyde (OPA)/ 9-fluorenylmethyl chloroformate (FMOC). A Thermo ODS Hypersil column was used for separation with sodium acetate buffer solution (containing triethylamine and THF) and sodium acetate buffer solution (containing acetonitrile and methanol) as the mobile phase for gradient elution. Samples were detected by HPLC under the detection wavelengths of 338 nm and 262 nm. Results Sixteen kinds of amino acids presented good linear relationships in the concentration range of 4~250 μg/mL. The recoveries spiked at the level of 10 μg/mL were ranged in 85.8%~115.2% with RSDs of 0.1%~9.1% (n=6), and the limits of detection were 0.2~4.6 ng. Conclusion This method is simple and sensitive, which can been used for the determination in practical sample.
查看全文  查看/发表评论  下载PDF阅读器