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Determination of a new illegal additive, vardenafil impurity 31 by ultra performance liquid chromatography-tandem mass spectrometry
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Yu-Chun DING1, Wei HU1, Zhi-Ying BAO1, Meng-Ying WANG1, Xiao-Ting TONG1, Hui XU2, Meng-Xing CHENG1, *
Journal of Food Safety & Quality | 2025, 16(11) : 193 - 199
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Journal of Food Safety & Quality | 2025, 16(11): 193-199
Special Topic: Analysis and Monitoring of Toxic and Harmful Substances in Food
Determination of a new illegal additive, vardenafil impurity 31 by ultra performance liquid chromatography-tandem mass spectrometry
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Yu-Chun DING1, Wei HU1, Zhi-Ying BAO1, Meng-Ying WANG1, Xiao-Ting TONG1, Hui XU2, Meng-Xing CHENG1, *
Affiliations
  • 1. Jiangxi Qiushi Judicial Identification Center, Nanchang 330000, China
  • 2. Agilent Technologies Technology (China) Co., Ltd., Shanghai 200000, China
Published: 2025-06-15 doi: 10.19812/j.cnki.jfsq11-5956/ts.20240911002
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Objective To establish a method for the qualitative and quantitative determination of a new illegal additive in foods, vardenafil impurity 31 by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Methods The UPLC-MS/MS was used to screen 92 kinds of substances of nafils illegally added in foods. The ultra performance liquid chromatography-high resolution mass spectrometry (UPLC-HRMS) was used to analyze the structure of the test sample. After the structure was inferred, the standard substance was purchased and verified. The target substance in the test sample was confirmed to be vardenafil impurity 31. The multiple reaction monitoring (MRM) method was established by UPLC-MS/MS, which was suitable for the qualitative and quantitative determination of vardenafil impurity 31 in foods. Results The limit of detection of vardenafil impurity 31 was 5 μg/kg, and the limit of quantitation was 10 μg/kg. The linear relationship was good in the linear range of 0.1-50.0 ng/mL, the correlation coefficient (r) was 0.9976, the average recovery rate was 85.33%-89.41%, and the relative standard deviation (RSD) was less than 10%. Conclusion The established method is simple and accurate, and can be used for the qualitative and quantitative determination of the new illegal additive vardenafil impurity 31 in foods.

ultra performance liquid chromatography-tandem mass spectrometry  /  high resolution mass spectrometry  /  illegal additives
Yu-Chun DING, Wei HU, Zhi-Ying BAO, Meng-Ying WANG, Xiao-Ting TONG, Hui XU, Meng-Xing CHENG. Determination of a new illegal additive, vardenafil impurity 31 by ultra performance liquid chromatography-tandem mass spectrometry[J]. Journal of Food Safety & Quality, 2025 , 16 (11) : 193 -199 . DOI: 10.19812/j.cnki.jfsq11-5956/ts.20240911002
Year 2025 volume 16 Issue 11
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doi: 10.19812/j.cnki.jfsq11-5956/ts.20240911002
  • Receive Date:2024-09-11
  • Online Date:2025-07-14
  • Published:2025-06-15
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  • Received:2024-09-11
Affiliations
    1. Jiangxi Qiushi Judicial Identification Center, Nanchang 330000, China
    2. Agilent Technologies Technology (China) Co., Ltd., Shanghai 200000, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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