Optimising QuEChERS method for determining five amanita peptide toxins in mixed wild mushrooms

Introduction: this study establishes an optimised quick, easy, cheap, effective, rugged and safe (QuEChERS) method integrated with high-performance liquid chromatography–tandem mass spectrometry for detecting five amatoxins in wild mushrooms. Methods: samples were ultrasonically extracted using a methanol-water mixture and purified using an adsorbent. The separation of the five amatoxins was performed in a C 18 column using 5-mmol/L ammonium formate solution (0.1% formic acid) and acetonitrile as the mobile phases. The five peptide toxins exhibit a remarkable linear relationship in the range of 10-500 μg/L. Results: the limits of detection and quantification were 8-13 and 26-42 μg/kg, respectively. Moreover, recoveries ranged from 80.1% to 120.3%. The peptide toxin can still be detected in a mixed sample containing positive and negative samples. Conclusion: this method is simple, accurate and suitable for detecting amatoxins in mixed wild mushrooms. It holds significant potential for addressing wild mushroom poisoning incidents and enhancing food safety regulation.

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Publication Details

Journal
Measurement Food
Published
2025-09-01
DOI
https://doi.org/10.1016/j.meafoo.2025.100247
Primary Topic
Silymarin and Mushroom Poisoning
Type
article
Field-Weighted Citation Impact
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article

Optimising QuEChERS method for determining five amanita peptide toxins in mixed wild mushrooms

Yuan Huang, Yan Zhang, Xing Xu, JiYan Duan et al.
Measurement Food
Silymarin and Mushroom Poisoning
article

Optimising QuEChERS method for determining five amanita peptide toxins in mixed wild mushrooms

Yuan Huang, Yan Zhang, Xing Xu, JiYan Duan, QiXin Guo
article en

Abstract

Introduction: this study establishes an optimised quick, easy, cheap, effective, rugged and safe (QuEChERS) method integrated with high-performance liquid chromatography–tandem mass spectrometry for detecting five amatoxins in wild mushrooms. Methods: samples were ultrasonically extracted using a methanol-water mixture and purified using an adsorbent. The separation of the five amatoxins was performed in a C 18 column using 5-mmol/L ammonium formate solution (0.1% formic acid) and acetonitrile as the mobile phases. The five peptide toxins exhibit a remarkable linear relationship in the range of 10-500 μg/L. Results: the limits of detection and quantification were 8-13 and 26-42 μg/kg, respectively. Moreover, recoveries ranged from 80.1% to 120.3%. The peptide toxin can still be detected in a mixed sample containing positive and negative samples. Conclusion: this method is simple, accurate and suitable for detecting amatoxins in mixed wild mushrooms. It holds significant potential for addressing wild mushroom poisoning incidents and enhancing food safety regulation.

Measurement FoodVol. 19
Dali University (CN)
Openalex Percentile: Top 66%
Silymarin and Mushroom Poisoning
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