A modified QuEChERS method coupled with liquid chromatography-tandem mass spectrometry for the simultaneous detection and quantification of scopolamine, L-hyoscyamine, and sparteine residues in animal-derived food products

被引:25
作者
Zheng, Weijia [1 ]
Yoo, Kyung-Hee [1 ]
Choi, Jeong-Min [1 ]
Park, Da-Hee [1 ]
Kim, Seong-Kwan [1 ]
Kang, Young-Sun [1 ,2 ]
Abd El-Aty, A. M. [3 ,4 ]
Hacimuftuoglu, Ahmet [4 ]
Jeong, Ji Hoon [5 ]
Bekhit, Alaa El-Din [6 ]
Shim, Jae-Han [7 ]
Shin, Ho-Chul [1 ]
机构
[1] Konkuk Univ, Dept Vet Pharmacol & Toxicol, Coll Vet Med, Seoul 143701, South Korea
[2] Konkuk Univ, Dept Biomed Sci & Technol, Seoul 143701, South Korea
[3] Cairo Univ, Dept Pharmacol, Fac Vet Med, Giza 12211, Egypt
[4] Ataturk Univ, Med Fac, Dept Med Pharmacol, TR-25240 Erzurum, Turkey
[5] Chung Ang Univ, Dept Pharmacol, Coll Med, 221 Heuksuk Dong, Seoul 156756, South Korea
[6] Univ Otago, Dept Food Sci, POB 56, Dunedin, New Zealand
[7] Chonnam Natl Univ, Coll Agr & Life Sci, Nat Prod Chem Lab, 300 Yongbong Dong, Gwangju 500757, South Korea
关键词
Scopolamine; L-hyoscyamine; Sparteine; Porcine muscle; Egg; Milk; QuEChERS; Residues; LC-MS/MS; TROPANE ALKALOIDS; PESTICIDE-RESIDUES; EXTRACTION; ATROPINE; PYRROLIZIDINE; VALIDATION; URINE; MILK;
D O I
10.1016/j.jare.2018.09.004
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We developed a modified Quick, Easy, Cheap, Effective, Rugged, and Safe (CEN QuEChERS) extraction method coupled with liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI+/MS-MS) to identify and quantify residues of three botanical alkaloids, namely, scopolamine, L-hyoscyamine, and sparteine, in animal-derived foods, including porcine muscle, egg, and milk. A combination of ethylenediaminetetraacetic acid disodium buffer and acetonitrile acidified with 0.5% trifluoroacetic acid was used as an extraction solvent, whereas QuEChERS (CEN, 15662) kits and sorbents were applied for cleanup procedures. The proposed method was validated by determining the limits of quantification (LOQs), with values of 1-5 mu g/kg achieved for the target analytes in various matrices. Linearity was estimated from matrix-matched calibration curves constructed using six concentration levels ranging from 1- to 6-fold increases in the LOQs of each analyte, and the correlation coefficients (R-2) were >= 0.9869. Recoveries (at three concentration levels of 1-, 2-, and 3-fold increases in the LOQ) of 73-104% were achieved with relative standard deviations (RSDs) <= 7.7% (intra-day and inter- day precision). Ten types of each matrix procured from large markets were evaluated, and all tested samples showed negative results. The current protocol is simple and versatile and can be used for routine detection of plant alkaloids in animal food products. (C) 2018 Production and hosting by Elsevier B.V. on behalf of Cairo University.
引用
收藏
页码:95 / 102
页数:8
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