Determination of synephrine in feeds by a novel quick, easy, cheap, effective, rugged, and safe solid-phase extraction method combined with UHPLC-MS/MS

被引:7
|
作者
Song, Yue [1 ,2 ]
Chai, Tingting [3 ]
Lou, Shengting [1 ,2 ]
Zhao, Yuechen [1 ,2 ]
Zhang, Xining [1 ,2 ]
Yang, Shuming [1 ,2 ]
Qian, Yongzhong [1 ,2 ]
Qiu, Jing [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Inst Qual Stand Testing Technol Agroprod, Key Lab Agroprod Qual & Safety, Beijing 100081, Peoples R China
[2] Minist Agr, Key Lab Agrifood Qual & Safety, Beijing, Peoples R China
[3] Zhejiang A&F Univ, Coll Agr & Food Sci, Key Lab Qual Improvement Agr Prod Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
关键词
feed; solid-phase extraction; synephrine; tandem mass spectrometry; ultra high performance liquid chromatography; PORTAL HYPERTENSIVE-RATS; CITRUS-AURANTIUM; P-SYNEPHRINE; DIETARY-SUPPLEMENTS; CAPILLARY-ELECTROPHORESIS; FRUIT; SEPARATION; PRODUCTS; EXERCISE; PEEL;
D O I
10.1002/jssc.201701194
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To detect and quantify synephrine in feed, an effective analytical method based on quick, easy, cheap, effective, rugged, and safe solid-phase extraction coupled to ultra high performance liquid chromatography with tandem mass spectrometry was developed with isotopic internal standards. Pretreatment was performed using quick, easy, cheap, effective, rugged, and safe solid-phase extraction with primary secondary amine and C18 sorbent as sorbents in combination with Oasis MCX column cleanup to extract and purify feed samples. Tandem mass spectrometry detection in positive ion mode was conducted in positive multiple reaction monitoring mode in addition to the quantitative internal standard method. Two transitions of synephrine at m/z 168.1/150.0 and 168.1/135.0 were selected, and m/z 168.1/135.0 was determined as the quantification ion pair. D-9-Terbutaline was selected as an internal standard, for which m/z 235.1/153.0 was selected as the quantification ion pair. Good linearity was shown for synephrine in the range of 0.5-50 mu g/L, and the correlation coefficient exceeded 0.999. The recoveries in three different feed samples at three spiked levels were 81.42-112.08%, and the relative standard deviations were not greater than 14.66%. The method proposed in this study was reliable and highly effective, and its sensitivity, accuracy, and precision are suitable for determining synephrine residues in feed samples.
引用
收藏
页码:1743 / 1751
页数:9
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