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作 者:陈丽娟[1] 费晓庆[1] 谭梦茹 吴斌[1] 沈崇钰[1] 张睿[1] 丁涛[1] 刘芸[1] 杨功俊[2]
机构地区:[1]江苏出入境检验检疫局食品实验室,江苏南京210001 [2]中国药科大学药学院,江苏南京211198
出 处:《分析测试学报》2016年第9期1142-1146,共5页Journal of Instrumental Analysis
基 金:国家质检总局科技计划项目(2015IK138);江苏出入境检验检疫局科技计划项目(2015KJ31);国家自然科学基金资助项目(21275162)
摘 要:建立了蜂蜜中苯甲酸、山梨酸、安赛蜜、糖精钠的超高效液相色谱-高分辨质谱分离测定方法。样品采用甲醇-水溶液(10∶90)提取,Diamonsil Plus C18色谱柱进行色谱分离,以0.5 mmol/L乙酸铵溶液和甲醇为流动相梯度洗脱,通过高分辨负离子扫描模式进行定性,外标法定量。结果表明,4种物质在0.02~2.0 mg/L范围内均具有良好的线性关系,相关系数为0.998 7~0.999 7。苯甲酸、山梨酸的方法定量下限为0.5 mg/kg,安赛蜜、糖精钠为0.3 mg/kg 。在低、中、高3个加标浓度下,方法的回收率为89.0%~104.0%,相对标准偏差(RSD)为2.0%~7.9%。该方法灵敏、简单、快速,定性准确可靠,适用于大批量蜂蜜中苯甲酸、山梨酸、安赛蜜、糖精钠的检测。A method based on ultra high performance liquid chromatography-high resolution mass spectrometry was developed to separate benzoic acid,sorbic acid,acesulfame-K and saccharin sodium in honey.The targeted compounds in honey samples were extracted with methanol-water mixtures(10∶90),and separated on a Diamonsil Plus C18 column with 0.5 mmol/L ammonium acetate-methanol as mobile phase by gradient elution.The qualitative and quantitative analyses were operated under t-MS2 by high resolution mass spectrometry with the external standard method.The results indicated that four analytes had good linearities in the concentration range of 0.02-2.0 mg/L with correlation coefficients of 0.998 7-0.999 7.The quantilition limits for benzoic acid,sorbic acid,acesulfame-K and saccharin sodium were 0.5,0.5,0.3,0.3 mg/kg,respectively.The recoveries of four compounds at three spiked levels were in the range of 89.0%-104.0%,with relative standard deviations(RSDs) of 2.0%-7.9%.The method was simple and rapid,and was suitable for the determination of benzoic acid,sorbic acid and acesulfame-K,saccharin sodium in honey.
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