Zheng Weijia, Park Jin-A, Abd El-Aty A M, Kim Seong-Kwan, Cho Sang-Hyun, Choi Jeong-Min, Yi Hee, Cho Soo-Min, El-Banna H A, Shim Jae-Han, Chang Byung-Joon, Wang Jing, Kim Jin-Suk, Shin Ho-Chul
Department of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Konkuk University, Seoul 143-701, Republic of Korea.
Department of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Konkuk University, Seoul 143-701, Republic of Korea; Department of Pharmacology, Faculty of Veterinary Medicine, Cairo University, Giza 12211, Egypt.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Oct 1;1064:100-108. doi: 10.1016/j.jchromb.2017.08.035. Epub 2017 Aug 31.
Herein, we developed a simple analytical procedure for the quantitation of bithionol residues in animal-derived food products such as porcine muscle, eggs, milk, eel, flatfish, and shrimp using a modified quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction method coupled with liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI/MS-MS). Samples were extracted with 0.1% solution of formic acid in acetonitrile and the extract was purified using a C18 sorbent. Separation was performed on a Waters XBridge™ C18 reversed-phase analytical column using 0.1% solution of formic acid/acetonitrile as the mobile phase. Six-point matrix-matched calibration indicated good linearity, with the calculated coefficients of determination (R) being≥0.9813. Intra- and inter-day recoveries (determined at spiking levels equivalent to 1×and 2×the limit of quantitation (0.25μg/kg)) ranged between 80.0 and 94.0%, with the corresponding relative standard deviations (RSDs) being≤8.2%. The developed experimental protocol was applied to different samples purchased from local markets in Seoul, which were tested negative for bithionol residues. In conclusion, the proposed method proved to be versatile and precise, being ideally suited for the routine detection of bithionol residues in animal-derived food products with various protein and fat contents.
在此,我们开发了一种简单的分析方法,用于定量检测动物源性食品(如猪肌肉、鸡蛋、牛奶、鳗鱼、比目鱼和虾)中的硫双二氯酚残留。该方法采用改良的快速、简便、廉价、高效、耐用且安全(QuEChERS)提取方法,并结合液相色谱 - 电喷雾电离串联质谱(LC - ESI/MS - MS)。样品用0.1%的甲酸乙腈溶液提取,提取物用C18吸附剂净化。在 Waters XBridge™ C18反相分析柱上进行分离,以0.1%的甲酸/乙腈溶液作为流动相。六点基质匹配校准显示出良好的线性,计算得到的决定系数(R)≥0.9813。日内和日间回收率(在相当于定量限(0.25μg/kg)的1倍和2倍加标水平下测定)在80.0%至94.0%之间,相应的相对标准偏差(RSD)≤8.2%。所开发的实验方案应用于从首尔当地市场购买的不同样品,这些样品经检测硫双二氯酚残留均为阴性。总之,所提出的方法被证明是通用且精确的,非常适合常规检测各种蛋白质和脂肪含量的动物源性食品中的硫双二氯酚残留。