马作江,柏 雪,蔡 学,黄 波,谢义梅,单长海,刘必英.超高压液相色谱-串联质谱法快速测定酒类中的 4种甜味剂[J].食品安全质量检测学报,2013,4(4):1185-1189
超高压液相色谱-串联质谱法快速测定酒类中的 4种甜味剂
Rapid determination of four sweeteners content in liquor by ultra pressure liquid chromatography-mass spectrometry
投稿时间:2013-07-22  修订日期:2013-08-15
DOI:
中文关键词:  超高压液相色谱-串联质谱联用    甜味剂
英文关键词:ultra pressure liquid chromatography- mass spectrometry(UPLC-MS/MS)  liquor  sweeteners
基金项目:
作者单位
马作江 恩施土家族苗族自治州产品质量监督检验所 
柏 雪 恩施土家族苗族自治州产品质量监督检验所 
蔡 学 恩施土家族苗族自治州产品质量监督检验所 
黄 波 恩施土家族苗族自治州产品质量监督检验所 
谢义梅 恩施土家族苗族自治州产品质量监督检验所 
单长海 恩施土家族苗族自治州产品质量监督检验所 
刘必英 恩施土家族苗族自治州产品质量监督检验所 
AuthorInstitution
MA Zuo-Jiang Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
BAI Xue Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
CAI Xue Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
HUANG Bo Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
XIE Yi-Mei Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
SHAN Chang-Hai Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
LIU Bi-Ying Enshi Tujia and Miao Autonomous Prefecture Product Quality Supervision and Inspection Institute 
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中文摘要:
      目的 建立酒类中安赛蜜、糖精钠、甜蜜素和三氯蔗糖4种甜味剂的超高压液相色谱-串联质谱联用(UPLC-MS/MS)快速测定方法。方法 采用Agilent ZORBAX SB-C18色谱柱(50 mm?2.1 mm, 1.8 μm)分离, 以0.1%甲酸水溶液-甲醇作为流动相梯度洗脱, 在电喷雾离子源ESI负离子模式下多重反应监测(MRM)定性、定量测定甜味剂。结果 4种甜味剂在10~500 μg/L的范围内与峰面积有良好的线性关系, 相关系数大于0.99, 检出限为0.5~2.4 μg/L, 加标回收率在89.4%~104.6%之间, RSD小于4 %。结论 该方法简便灵敏, 准确快速, 可用于酒类食品中低剂量、复合甜味剂的测定。
英文摘要:
      Objective To establish a rapid determination method of four sweeteners(acesulfame, saccharin sodium, sodium cyclamate and suralose) in liquors by ultra pressure liquid chromatography-mass spectrometry (UPLC-MS/MS). Methods The samples were separated by Agilent ZORBAX SB-C18 column(50 mm×2.1 mm, 1.8 μm) using 0.1% formic acid water-methanol as mobile phase and analyzed by electrospray ionization (ESI) in the negative ion and multiple reaction monitoring mode (MRM). Results The method showed a good linearity over the range of 10?500 μg/L. The average recoveries were 89.4%?104.6% with RSD less than 4%. The quantitative limits of four sweeteners were 0.5?2.4 μg/L. Conclusion This method is accurate, rapid, and highly sensitive and it is suitable for the determination of low concentration sweeteners in liquors.
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