Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Hidalgo, Carr. Pachuca-Tulancingo Km. 4.5, 42076, Pachuca, Hgo, Mexico.
J Chromatogr A. 2011 Apr 22;1218(16):2196-202. doi: 10.1016/j.chroma.2011.02.046. Epub 2011 Feb 25.
A magnetic solid phase extraction method coupled to capillary electrophoresis is proposed for the determination of tetracycline, oxytetracycline, chlortetracycline and doxycycline in milk samples. Five different magnetic phenyl silica adsorbents covered with magnetite were synthesized by varying the molar ratio of phenyltrimethylsilane and tetramethylorthosilicate; these adsorbents were evaluated in terms of their pH and degree of hydrophobicity for tetracycline retention. The optimal, selected combination of conditions was a pH of 10.0 and a magnetic sorbent ratio of 4:1; under these conditions, the retention capacity ranged from 99.7% to 101.2% for the four tetracyclines analyzed. The elution conditions and initial sample volume of the proposed extraction method were also optimized, and the best results were obtained with 1×10(-3) M acetic acid in methanol as eluent and a 200 ml of sample volume. Under optimal conditions, average recoveries ranged from 94.2% to 99.8% and the limits of detection ranged from 2 to 9 μg l(-1) for the four tetracyclines. After the proposed method was optimized and validated, 25 milk samples of different brands were analyzed, oxytetracycline residues were detected in five samples, in concentrations ranging from 98 to 213 μg l(-1). Subsequent analysis of positive samples by SPE-CE and magnetic solid phase extraction-HPLC revealed than no significant differences were found from results obtained by the proposed methodology. Thus, the developed magnetic extraction is a robust pre-concentration technique that can be coupled to other analytical methods for the quantitative determination of tetracyclines.
提出了一种将磁固相萃取与毛细管电泳相结合的方法,用于测定牛奶样品中的四环素、土霉素、金霉素和强力霉素。通过改变苯基三甲基硅烷和四甲氧基硅烷的摩尔比,合成了五种不同的覆盖有磁铁矿的磁性苯基硅胶吸附剂;这些吸附剂在 pH 值和对四环素保留的疏水性方面进行了评价。选择的最佳条件组合为 pH 值为 10.0 和磁固相比为 4:1;在这些条件下,四种四环素的保留率范围为 99.7%至 101.2%。还优化了建议的萃取方法的洗脱条件和初始样品量,最佳结果是使用 1×10(-3) M 甲醇中的乙酸作为洗脱液和 200 ml 样品量。在最佳条件下,四种四环素的平均回收率范围为 94.2%至 99.8%,检测限范围为 2 至 9 μg l(-1)。在对建议的方法进行优化和验证后,分析了 25 个不同品牌的牛奶样品,在五个样品中检测到土霉素残留,浓度范围为 98 至 213 μg l(-1)。随后对阳性样品进行 SPE-CE 和磁固相萃取-HPLC 分析,结果表明与所建议的方法获得的结果没有显著差异。因此,开发的磁性萃取是一种强大的预浓缩技术,可与其他分析方法结合用于定量测定四环素。