肉味香精中5-羟甲基糠醛的含量测定

目的建立肉味香精中5-羟甲基糠醛的高效液相色谱分析方法。方法香精样品经甲醇溶液提取后离心,将所得上清液过滤后采用高效液相色谱分析。测定条件为：Venusil XBP-C18色谱柱,UV检测器的检测波长为284 nm,以甲醇-水溶液（5：95,V：V）为流动相,流速为1.0 mL/min,柱温30℃。结果本方法能在25 min内完成目标化合物的分离分析。5-HMF标准品在0.16-40.00μg/mL的浓度范围内呈良好的线性关系,r^2=0.9999,方法的检出限为0.3525μg/L,定量限为2.82μg/L。5-HMF在3个添加水平的平均回收率为86.89%,能够满足样品测定的要求。自制糖醋...

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Published in食品安全质量检测学报 Vol. 7; no. 10; pp. 4021 - 4026
Main Author 张莉莉 孙颖 孔琰 杨肖 张玉玉 孙宝国 陈海涛
Format Journal Article
LanguageChinese
Published 北京食品营养与人类健康高精尖创新中心，食品质量与安全北京实验室，北京市食品风味化学重点实验室，北京工商大学，北京 100048 2016
Subjects
5-羟甲基糠醛
肉味香精
高效液相色谱法
高效液相色谱法
肉味香精
high performance liquid chromatography
5-羟甲基糠醛
meat flavor
5-hydroxymethylfurfural
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Summary:目的建立肉味香精中5-羟甲基糠醛的高效液相色谱分析方法。方法香精样品经甲醇溶液提取后离心,将所得上清液过滤后采用高效液相色谱分析。测定条件为：Venusil XBP-C18色谱柱,UV检测器的检测波长为284 nm,以甲醇-水溶液（5：95,V：V）为流动相,流速为1.0 mL/min,柱温30℃。结果本方法能在25 min内完成目标化合物的分离分析。5-HMF标准品在0.16-40.00μg/mL的浓度范围内呈良好的线性关系,r^2=0.9999,方法的检出限为0.3525μg/L,定量限为2.82μg/L。5-HMF在3个添加水平的平均回收率为86.89%,能够满足样品测定的要求。自制糖醋排骨香精中5-HMF的含量为7.80 mg/kg,市售猪肉、牛肉和鸡肉香精中5-HMF的平均含量分别为3.94、5.32和9.38 mg/kg,且测定结果间的RSD平均值为均小于5%。结论该方法快速、准确、灵敏,适用于肉味香精中5-羟甲基糠醛的定量分析。
Bibliography:ZHANG Li-Li, SUN Ying, KONG Yan, YANG Xiao, ZHANG Yu-Yu, SUN Bao-Guo, CHEN Hai-Tao （Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Laboratory for Food Quality and Safety, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, Beijing 100048, China）
11-5956/TS
meat flavor; 5-hydroxymethylfurfural; high performance liquid chromatography
Objective To establish a method for the determination of 5-hydroxymethylfurfural in meat flavors by high performance liquid chromatography（HPLC）.Methods The flavor samples were extracted with methanol and then centrifuged,and after being filtered,the supernatant fluid obtained was analyzed by HPLC.The samples were analyzed on a Venusil XBP-C_（18） column at 284 nm with a UV detector.Using the methanol water solution（5：95,V：V）as mobile phase with the flow rate was 1.0 mL/min and the column temperature was 30 °C.Results The separation and analysis of the target compound were accomplished within 25 min using this method.
ISSN:2095-0381