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作 者:朱晓月[1] 施捷[1] 张喆[1] 胡琴[1] 车宝泉[1] 丛骆骆
机构地区:[1]北京市药品检验所,北京100035 [2]北京市食品药品监督管理局,北京100053
出 处:《药物分析杂志》2014年第10期1817-1822,共6页Chinese Journal of Pharmaceutical Analysis
基 金:北京市科技计划(Z111100074211021)
摘 要:目的:建立一种实时直接分析质谱法快速筛查葡萄酒中安赛蜜、阿斯巴甜、纽甜、甘草次酸、麦芽糖醇、异麦芽酮糖、木糖醇、D-山梨醇、D-甘露醇共9种甜味剂。方法:实时直接分析离子源串联三重四极杆质谱,源电压为350 V,载气为氦气,源温度350℃,样品传输速度为2 mm·s-1,采用子离子扫描模式直接分析葡萄酒样品,通过对照品与样品的二级质谱图对比进行非法添加成分的定性鉴别。结果:9种甜味剂检出限为2.5~20μg·mL-1,5批样品中检出麦芽糖醇、异麦芽酮糖、D-山梨醇及D-甘露醇,同时阐释了9种甜味剂的二级质谱裂解途径。结论:方法简单快速,每次检测时间仅需几秒,检测效率比液质联用法提高近25倍,适用于大批量葡萄酒中甜味剂类成分的快速筛查。Objective: To develop a rapid analysis method of 9 sweeteners : acesulfame K, aspartame, neotame, glycyr- rhetic acid,lactitol, palatinose, xylitol, D - sorbitol and D - mannitol in wines. Methods: Triple quadrupol MS with DART ion source was used to perform the direct analysis. The source voltage of DART was 350 V. The temperature was 350 ℃. The DART sampler delivery rate was 2 mm · s-1. Daughter scan mode was directly used to analyze the sam- ples. The identification was performed by comparing the mass spectra of detected peaks in samples with the mass spec- tra of peaks in reference substance. Results: The limits of detection for 9 sweeteners ranged from 2.5 μg · mL- 1 to 20 μg · mL-1. Lactitol ,palatinose ,D - sorbitol and D - mannitol were detected in 5 samples. Additionally ,the fragmenta- tion pathways of the 9 sweeteners were speculated. Conclusion: The method is easy and accurate. The time of once detection is only several seconds. The efficiency of detection is improved by about 25 times compared with HPLC - MS. The method can be used to rapidly detect and identify the 9 sweeteners in abundant batch of wines.
关 键 词:实时直接分析质谱 甜味剂 葡萄酒 快速筛查 安赛蜜 阿斯巴甜 纽甜 甘草次酸 麦芽糖醇 异麦芽酮糖 木糖醇 山梨醇 甘露醇
分 类 号:R917[医药卫生—药物分析学]
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