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Rapid detection of aflatoxin B1 and zearalenone content in Zea mays L. by molecularly imprinted-surface-enhanced Raman spectroscopy technology
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Yuan WANG1, 2, Ai-Li ZHANG2, Meng WANG2, Kai-Xu BAI3, Hong-Jun WANG3, Yu WANG1, *, Wen-Lei ZHAI2, *
Journal of Food Safety & Quality | 2026, 17(13) : 3 - 12
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Journal of Food Safety & Quality | 2026, 17(13): 3-12
• Special Topic: Detection and Prevention and Control of Biotoxins in Food •
Rapid detection of aflatoxin B1 and zearalenone content in Zea mays L. by molecularly imprinted-surface-enhanced Raman spectroscopy technology
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Yuan WANG1, 2, Ai-Li ZHANG2, Meng WANG2, Kai-Xu BAI3, Hong-Jun WANG3, Yu WANG1, *, Wen-Lei ZHAI2, *
Affiliations
  • 1.School of Food Science and Engineering, Shanxi Agricultural University, Jinzhong 030801, China
  • 2.Institute of Quality Standard and Testing Technology, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China
  • 3.China Grain Reserves Group Co., Ltd., Shanxi Branch, Taiyuan 030000, China
doi: 10.19812/j.cnki.jfsq11-5956/ts.20260203003
Outline
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Objective

To establish a method for rapid determination of the aflatoxin B1 (AFB1) and zearalenone(ZEN) in Zea mays L. by molecularly imprinted-surface‑enhanced Raman spectroscopy (SERS).

Methods

Dual‑template molecularly imprinted materials were prepared and used for the pretreatment and purification of Zea mays L.. Ag nanoparticles were employed as the SERS‑active substrate, and a label‑free detection method was developed based on the characteristic SERS peaks of AFB1 and ZEN. The effects of molecularly imprinted materials preparation conditions and SERS detection parameters (including substrate concentration and type of aggregating agent)on the analytical performance were investigated.

Results

Under the optimized conditions, dual‑template molecularly imprinted materials pretreatment (template-to-monomer molar ratio of 1:2), Ag nanoparticles concentration of 0.56 mmol/L, and potassium bromide and magnesium chloride as aggregating agents for AFB1 and ZEN, respectively. The limits of detection were 1.5 ng/mL for AFB1 and 5.0 ng/mL for ZEN. The linear ranges for both toxins were 10–1000 ng/mL, with determination coefficients of 0.9268 for AFB1 and 0.9611 for ZEN. The average recoveries ranged from 93.29% to 96.10%, and the relative standard deviations were all below 5%.

Conclusion

The established method is simple, rapid, accurate, and suitable for on‑site rapid screening of AFB1 and ZEN in Zea mays L. powder.

surface‑enhanced Raman spectroscopy technology  /  molecularly imprinted technology  /  Zea mays L.  /  aflatoxin B1  /  zearalenone
王渊, 张爱栎, 王蒙, 白凯旭, 王红军, 王愈, 翟文磊. 分子印迹‑表面增强拉曼光谱技术快速检测玉米中黄曲霉毒素B1和玉米赤霉烯酮含量. 食品安全质量检测学报, 2026 , 17 (13) : 3 -12 . DOI: 10.19812/j.cnki.jfsq11-5956/ts.20260203003
Yuan WANG, Ai-Li ZHANG, Meng WANG, Kai-Xu BAI, Hong-Jun WANG, Yu WANG, Wen-Lei ZHAI. Rapid detection of aflatoxin B1 and zearalenone content in Zea mays L. by molecularly imprinted-surface-enhanced Raman spectroscopy technology[J]. Journal of Food Safety & Quality, 2026 , 17 (13) : 3 -12 . DOI: 10.19812/j.cnki.jfsq11-5956/ts.20260203003
Year 2026 volume 17 Issue 13
9
2
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doi: 10.19812/j.cnki.jfsq11-5956/ts.20260203003
  • Receive Date:2026-02-03
  • Online Date:2026-11-05
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  • Received:2026-02-03
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Affiliations
    1.School of Food Science and Engineering, Shanxi Agricultural University, Jinzhong 030801, China
    2.Institute of Quality Standard and Testing Technology, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China
    3.China Grain Reserves Group Co., Ltd., Shanxi Branch, Taiyuan 030000, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
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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