谢强胜,王 慧,张子璇,王 坤,李启艳,胡德福.超高效液相色谱法测定酒精饮料中非法添加抗疲劳药物他达拉非及2种类似物[J].食品安全质量检测学报,2017,8(3):1030-1036
超高效液相色谱法测定酒精饮料中非法添加抗疲劳药物他达拉非及2种类似物
Determination of illegally added antifatigue drugs tadalafil and 2 analogues in alcoholic beverage by ultra performance liquid chromatography
投稿时间:2017-02-15  修订日期:2017-03-14
DOI:
中文关键词:  超高效液相色谱法  非法添加  抗疲劳药物  他达拉非  酒精饮料
英文关键词:ultra performance liquid chromatography  illegal addition  antifatigue drugs  tadalafil  alcoholic beverage
基金项目:
作者单位
谢强胜 山东省食品药品检验研究院 
王 慧 中国食品药品检定研究院 
张子璇 利兹大学 
王 坤 山东省食品药品检验研究院 
李启艳 山东省食品药品检验研究院 
胡德福 山东省食品药品检验研究院 
AuthorInstitution
XIE Qiang-Sheng Shandong Institute for Food and Drug Control 
WANG Hui Naional Institutes for Food and Drug Control 
ZHANG ZI-Xuan University of Leeds 
WANG Kun Shandong Institute for Food and Drug Control 
LI Qi-Yan Shandong Institute for Food and Drug Control 
HU De-Fu Shandong Institute for Food and Drug Control 
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中文摘要:
      目的 建立超高效液相色谱法测定酒饮料中他达拉非和2种类似物的分析方法。方法 采用Agillent Zorbax SB-C18 (2.1 mm×50 mm, 1.8 μm)色谱柱, 二极管阵列检测器, 检测波长为290 nm, 流速为0.3 mL/min, 流动相A为0.1%乙酸铵溶液 (pH=3.4), 流动相B为乙腈, 按梯度进行洗脱。结果 氨基他达拉非、去甲基他达拉非、他达拉非分别在0.6~120、0.493~98.6、0.56~112 mg/L范围内呈现良好的线性关系, 检出限分别是0.6、0.6、0.5 ng, 方法精密度分别为0.92%、1.1%、0.68%(n=6), 平均回收率分别为101.8%、101.8%、101.7%, RSD分别为1.5%、0.87%、0.64%(n=6)。结论 该方法前处理简单、分析时间短、灵敏度高、重现性好, 可用于抗疲劳类化学药物在酒精饮料中非法添加的检测。
英文摘要:
      Objective To establish a method for the determination of tadalafil and other 2 analogues (amino tadalafil and dimethyl tadalafil) in alcoholic beverage by ultra performance liquid chromatography (UPLC). Methods Agilent Zorbax SB-C18 column (2.1 mm×50 mm, 1.8 μm) was used with a mobile phase consisting of acetonitrile and 0.01 mol/L ammonium acetate (pH=3.4) by gradient elution at a flow rate of 0.3 mL/min. The illegally added antifatigue drugs were detected by a photodiode array detector. The detection wavelength was set at 290 nm. Results The linearity ranges of amino tadalafil, dimethyl tadalafil and tadalafil were 0.6~120, 0.493~98.6, and 0.56~112 mg/L, respectively. The limits of determination were 0.6, 0.6, and 0.5 ng and the precisions of the method (RSDs) were 0.92%, 1.1% and 0.68% (n=6), respectively. The average recoveries were 101.8%, 101.8% and 101.7% (n=6) and the RSDs were 1.5%, 0.87% and 0.64% (n=6), respectively. Conclusion The established method has the advantages of simple sample pre-treatment, rapid detection, satisfactory recovery and good reproducibility, which is suitable for the determination of illegally added antifatigue drugs in alcoholic beverage.
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