Mookantsa S O S, Dube S, Nindi M M
Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, P.O. Box 392 UNISA, Pretoria, South Africa; Residue Section, Botswana National Veterinary Laboratory, P/Bag 0035, Gaborone, Botswana.
Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, P.O. Box 392 UNISA, Pretoria, South Africa.
Talanta. 2016 Feb 1;148:321-8. doi: 10.1016/j.talanta.2015.11.006. Epub 2015 Nov 4.
A rapid, cost effective and environmentally friendly extraction method, based on dispersive liquid-liquid microextraction (DLLME) was developed for the determination of six tetracyclines in meat destined for human consumption. Meat extracts were analysed for tetracyclines using liquid chromatography tandem mass spectrometry (LC-MS/MS), a sensitive and selective analytical technique. Various factors influencing the pre-concentration of tetracyclines such as sample pH, type and volume of both disperser solvent and extraction solvent were optimized. Validation parameters such as calibration function, limit of detection (LOD), limit of quantification (LOQ), detection capability (CCα), decision limit (CCβ), accuracy and precision were established according to Commission Decision 2002/657/EC. Linearity in the range of 25-200 µg kg(-1) was obtained with regression coefficients ranging from 0.9991 to 0.9998. Recoveries of spiked blank muscle samples at three levels (50, 100 and 150 µg kg(-1)) ranged from 80% to 105% and reproducibility was between 2% and 7%. LODs and LOQs ranged from 2.2 to 3.6 µg kg(-1) and from 7.4 to 11.5 µg kg(-1) respectively while CCα ranged from 105 to 111 µg kg(-1) and CCβ ranged from 107 to 122 µg kg(-1). The proposed method compared well with the existing accepted dispersive solid phase extraction method and was successfully applied to the pre-concentration and determination of tetracyclines in meat samples. Eleven of the thirty bovine muscle samples obtained from local abattoirs and butcheries were found to contain residues of two tetracycline antibiotics (chlortetracycline and oxytetracycline), with oxytetracycline being the most detected. Concentration levels of the tetracycline residues detected in bovine muscle samples were lower (12.4 and 68.9 µg kg(-1)) than the stipulated European Union maximum residue level (MRL) of 100 µg kg(-1), hence the meat was fit for human consumption. From this work it can be concluded that the DLLME is indeed a greener sample preparation method and could be used as an alternative to dispersive solid phase microextraction (dSPE).
基于分散液液微萃取(DLLME)开发了一种快速、经济高效且环保的萃取方法,用于测定供人类食用肉类中的六种四环素。使用液相色谱串联质谱法(LC-MS/MS)这一灵敏且具选择性的分析技术对肉类提取物中的四环素进行分析。对影响四环素预浓缩的各种因素进行了优化,如样品pH值、分散剂溶剂和萃取溶剂的类型及体积。依据欧盟委员会第2002/657/EC号决定确定了校准函数、检测限(LOD)、定量限(LOQ)、检测能力(CCα)、决策限(CCβ)、准确度和精密度等验证参数。在25 - 200 µg kg⁻¹范围内获得了线性关系,回归系数在0.9991至0.9998之间。三个加标水平(50、100和150 µg kg⁻¹)的空白肌肉样品回收率在80%至105%之间,重现性在2%至7%之间。LOD范围为2.2至3.6 µg kg⁻¹,LOQ范围为7.4至11.5 µg kg⁻¹,而CCα范围为105至111 µg kg⁻¹,CCβ范围为107至122 µg kg⁻¹。所提出的方法与现有的公认分散固相萃取方法相比效果良好,并成功应用于肉类样品中四环素的预浓缩和测定。从当地屠宰场和肉铺获取的30份牛肌肉样品中有11份被发现含有两种四环素类抗生素(金霉素和土霉素)残留,其中土霉素的检出率最高。牛肌肉样品中检测到的四环素残留浓度水平(12.4和68.9 µg kg⁻¹)低于欧盟规定的100 µg kg⁻¹最大残留限量(MRL),因此这些肉适合人类食用。由此工作可以得出结论,DLLME确实是一种更环保的样品制备方法,可作为分散固相微萃取(dSPE)的替代方法。