Evidence map›Paper›PMID 41969258›Full record

ArticleSe pu = Chinese journal of chromatography2026

[Determination of ergot alkaloids toxins in forage grass by ultra performance liquid chromatography-tandem mass spectrometry coupled with solid-phase supported liquid-liquid extraction].

Cai-Xia Ren, Xiao-Min Wang, Wan-Li Sheng, Yi-Zhi Han, Chun-Yan Zhang, Shu-Zhan Zheng

Abstract readEnglish Abstract
In one paragraph

Article in Se pu = Chinese journal of chromatography, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cai-Xia RenTechnical Center of Hohhot Customs,Hohhot 010020,China.
Xiao-Min WangTechnical Center of Hohhot Customs,Hohhot 010020,China.
Wan-Li ShengTechnical Center of Hohhot Customs,Hohhot 010020,China.
Yi-Zhi HanTechnical Center of Hohhot Customs,Hohhot 010020,China.
Chun-Yan ZhangTechnical Center of Hohhot Customs,Hohhot 010020,China.
Shu-Zhan ZhengTechnical Center of Hohhot Customs,Hohhot 010020,China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxic alkaloids, especially ergot alkaloid toxins, present in forage grass and pose serious health hazards to humans and livestock. Hence, a method for simultaneously detecting these dangerous plant toxins is needed. This study established a rapid method for detecting ten ergot alkaloid toxins using solid-phase supported liquid-liquid extraction technology combined with ultra performance liquid chromatography-tandem mass spectrometry. Forage samples were extracted with 8.0 mL of acetonitrile containing 1% formic acid. The extraction mixture was vortexed and then centrifuged at 8 000 r/min for 5 min, after which 1.0 mL of the supernatant was mixed with 3.0 mL of water and vortexed for 0.5 min. The entire mixture was transferred to a solid-phase supported liquid-liquid extraction column and allowed to stand for 10 min. The column was eluted with 6.0 mL of ethyl acetate and the collected eluate was evaporated under nitrogen at temperatures below 40 ℃. The residue was dissolved in 1 mL of acetonitrile-water (1∶3, volume ratio, containing 0.5% formic acid), and separated using an Acquity UPLC BEH C

Indexed as

Ergot AlkaloidsLiquid-Liquid ExtractionPoaceaeTandem Mass SpectrometryChromatography, High Pressure LiquidLiquid Chromatography-Mass SpectrometrySolid Phase ExtractionErgot Alkaloidsergot alkaloid toxinsforage grasssolid-phase supported liquid-liquid extractionultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)

Identifiers

PMID41969258
PMCPMC13077538

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