Determination of Nine Oxyphenisatin,Phenolphthalein and Their Derivants in Enzyme Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry
Experimental Techniques and Methods|更新时间:2025-03-17
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Determination of Nine Oxyphenisatin,Phenolphthalein and Their Derivants in Enzyme Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry
Journal of Instrumental AnalysisVol. 44, Issue 3, Pages: 500-505(2025)
LI Can,CHEN Tong-qiang,WANG Hui,LI Zheng,XIE Fang-yun,XIANG Jun,WANG Yun-hao,WANG Liang-liang.Determination of Nine Oxyphenisatin,Phenolphthalein and Their Derivants in Enzyme Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry[J].Journal of Instrumental Analysis,2025,44(03):500-505.
LI Can,CHEN Tong-qiang,WANG Hui,LI Zheng,XIE Fang-yun,XIANG Jun,WANG Yun-hao,WANG Liang-liang.Determination of Nine Oxyphenisatin,Phenolphthalein and Their Derivants in Enzyme Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry[J].Journal of Instrumental Analysis,2025,44(03):500-505. DOI: 10.12452/j.fxcsxb.240711209.
Determination of Nine Oxyphenisatin,Phenolphthalein and Their Derivants in Enzyme Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry
A new high performance liquid chromatography-tandem mass spectrometry method for screening and confirmation of the oxyphenisatin,phenolphthalein and their derivants in enzyme food was developed. The sample was extracted with acetonitrile-water,followed by centrifugation. The supernatant was then filtered through a membrane filter. The separation was performed on Hypersil Gold C
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column with gradient elution with 0.1% formic acid aqueous solution and 0.1% formic acid acetonitrile as mobile phases. The target compounds were determined by positive electrospray ionization under the multiple reaction monitoring(MRM) mode,which quantitative analysis by external standard method with matrix curve. Nine analytes showed good linear relationships in the range of 5-100 μg/L with correlation coefficients not less than 0.999 0. The results showed that the limit of quantification was 0.05 mg/kg. The average spiked recoveries showed a variation from 80.4%-101% for the three fortification levels,with relative standard deviations between 1.2% and 7.8%. This procedure was noticeably simple,rapid,sensitive and accurate. Therefore,this method is suitable for batch determination of the nine oxyphenisatin,phenolphthalein and their derivants in enzyme food.
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