Quantitative determination of carbasalate calcium derived metabolites, acetylsalicylic acid and salicylic acid, in six animal foods using liquid-liquid extraction method coupled with liquid chromatography-tandem mass spectrometry

被引:16
|
作者
Zheng, Weijia [1 ]
Yoo, Kyung-Hee [1 ]
Abd El-Aty, A. M. [2 ,3 ]
Park, Da-Hee [1 ]
Choi, Jeong-Min [1 ]
Kim, Seong-Kwan [1 ]
Kang, Young-Sun [1 ,4 ]
Zhang, Hongxia [5 ]
Hacimuftuoglu, Ahmet [3 ]
Bekhit, Alaa El-Din [6 ]
Wang, Jing [7 ]
Shim, Jae-Han [8 ]
Shin, Ho-Chul [1 ]
机构
[1] Konkuk Univ, Coll Vet Med, Dept Vet Pharmacol & Toxicol, Seoul 143701, South Korea
[2] Cairo Univ, Fac Vet Med, Dept Pharmacol, Giza 12211, Egypt
[3] Ataturk Univ, Med Fac, TR-25240 Erzurum, Turkey
[4] Konkuk Univ, Dept Biomed Sci & Technol, Seoul 143701, South Korea
[5] Qilu Univ Technol, Shandong Acad Sci, Coll Food Sci & Engn, State Key Lab Biobased Mat & Green Papermaking, POB 250353, Jinan, Shandong, Peoples R China
[6] Univ Otago, Dept Food Sci, POB 56, Dunedin, New Zealand
[7] Chinese Acad Agr Sci, Inst Qual Standard & Testing Technol Agroprod, Key Lab Agroprod Qual & Safety, Beijing 100081, Peoples R China
[8] Chonnam Natl Univ, Coll Agr & Life Sci, Nat Prod Chem Lab, 300 Yongbong Dong, Gwangju 500757, South Korea
关键词
Carbasalate calcium; Acetylsalicylic acid; Salicylic acid; Animal-derived foods; Residue; Liquid chromatography-tandem mass spectrometry; PESTICIDE-RESIDUES; HUMAN PLASMA; SAMPLE PREPARATION; SODIUM-SALICYLATE; ASPIRIN; PERFORMANCE; PRODUCTS; DRUGS;
D O I
10.1016/j.foodchem.2018.11.118
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work describes a simple screening protocol for quantification of carbasalate calcium derived metabolites, acetylsalicylic acid (ASA) and salicylic acid (SA), in animal and aquatic food matrices using liquid chromatography- tandem mass spectrometry (LC-MS/MS). The analytes were extracted from porcine muscle, milk, egg, shrimp, eel, and flatfish using acetonitrile, with the addition of formic acid as well as trifluoroacetic acid, followed by liquid-liquid purification with saturated n-hexane. A reverse-phase analytical column was employed with a mobile phase comprising (A) 1 mM ammonium acetate in distilled water and (B) methanol to achieve the best chromatographic separation. Matrix-matched calibration curves (R-2 >= 0.9817) were constructed using six concentrations of 5, 10, 20, 30, 40, and 50 mu g/kg in porcine muscle, milk, egg, shrimp, eel, and flatfish matrices. The calculated limits of quantification (LOQ) were 10 and 7 mu g/kg, for ASA and SA, respectively. Recoveries of 67 to 102% with relative standard deviations (RSDs) of <= 9.0% (intra-day and inter-day) were obtained for all matrices at four spiking concentrations (5, 10, 20, and 50 mu g/kg). The method was feasibly applied for monitoring market samples. In conclusion, the developed method is versatile, accurate, and precise for detecting and quantifying acetylsalicylic acid and salicylic acid residues in animal-derived foods meant for human consumption.
引用
收藏
页码:744 / 750
页数:7
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