Ferreira Débora Cecatto, de Toffoli Ana Lúcia, Maciel Edvaldo Vasconcelos Soares, Lanças Fernando Mauro
Institute of Chemistry of São Carlos, University of São Paulo, São Carlos, SP, Brazil.
Electrophoresis. 2018 Sep;39(17):2210-2217. doi: 10.1002/elps.201800053. Epub 2018 Jul 8.
Solid-phase extraction coupled online with high performance liquid chromatography and tandem mass spectrometry was successfully applied to determine low concentrations of ceftiofur antibiotic in bovine milk samples. A silica-anchored ionic liquid was applied as sorbent material to be used as extraction phase in the proposed online system. The material was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. In order to improve the system reproducibility, the following experimental parameters were optimized: organic solvent percentage, time and sample loading flow rate. Subsequently, the method was validated presenting satisfactory results as adequate selectivity, good linearity and correlation coefficient higher than 0.98. The limit of detection and quantification were 0.1 and 0.7 μg/L, respectively. The precision of the methodology was evaluated as repeatability and intermediate precision, with relative standard deviation values lower than 15%. The accuracy of the method ranged from 72.8 to 137% and the minimum and maximum recovery values were 73.4 and 111.3%, respectively. After the validation, seven milk samples were analyzed and although ceftiofur was not detected in any of them the method was demonstrated to be efficient when applied to the analysis of milk samples fortified with the pollutant of interest.
固相萃取与高效液相色谱和串联质谱联用,成功应用于测定牛奶样品中低浓度的头孢噻呋抗生素。一种硅胶锚定离子液体被用作吸附剂材料,作为所提出的在线系统中的萃取相。该材料通过傅里叶变换红外光谱和扫描电子显微镜进行表征。为了提高系统的重现性,对以下实验参数进行了优化:有机溶剂百分比、时间和样品加载流速。随后,该方法得到验证,呈现出令人满意的结果,具有足够的选择性、良好的线性和高于0.98的相关系数。检测限和定量限分别为0.1和0.7μg/L。该方法的精密度通过重复性和中间精密度进行评估,相对标准偏差值低于15%。该方法的准确度范围为72.8%至137%,最低和最高回收率分别为73.4%和111.3%。验证后,对七个牛奶样品进行了分析,尽管在任何样品中均未检测到头孢噻呋,但该方法在应用于分析添加了目标污染物的牛奶样品时被证明是有效的。