Charles University in Prague, Faculty of Pharmacy, Department of Analytical Chemistry, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
J Chromatogr B Analyt Technol Biomed Life Sci. 2013 May 15;927:201-8. doi: 10.1016/j.jchromb.2012.12.032. Epub 2013 Jan 9.
In this paper two fast and highly sensitive ultra-high performance liquid chromatography (UHPLC) methods for the determination of tetracycline antibiotics (oxytetracycline, tetracycline, doxycycline, demeclocycline, chlortetracycline, minocycline and degradation product epitetracycline) in surface waters have been developed using fluorescence (FL) and mass spectrometry (MS) detection. ACQUITY UPLC BEH C8 and ACQUITY CSH C18 columns were employed for FL and MS detection, respectively, both packed with 1.7μm particles. Mixed-mode separation mechanism of CSH (charged surface technology) sorbent was found particularly useful in analysis of TCs, which possess problematic amphoteric structures. The FL methodology was based on chelation of tetracyclines with calcium ions to perform on-column derivatisation. The developed methods were compared in the terms of validation parameters including linearity, sensitivity, precision and accuracy. The linearity range for FL detection was within 7ngmL(-1) to 50μgmL(-1) with method limit of detection (MLOD) as low as 0.2ngmL(-1) for most of the analytes. MS detection showed even higher sensitivity reaching MLOD of 0.003ngmL(-1), which is the highest sensitivity reported so far in analysis of TCs. Matrix matched calibration curves in the range of 0.01-50ngmL(-1) were used for quantification to compensate for matrix effects with the correlation coefficients demonstrating good linearity (0.9940-0.9999). The extraction of the antibiotics from surface waters was performed using solid phase extraction with Oasis HLB cartridges. Accuracy was expressed as recovery with values ranging from 96.52% to 127.30% and from 91.66% to 123.70% for FL and MS detection, respectively.
本文开发了两种快速、高灵敏度的超高效液相色谱(UHPLC)方法,用于荧光(FL)和质谱(MS)检测地表水四环素抗生素(土霉素、四环素、强力霉素、去甲金霉素、金霉素、米诺环素和降解产物表四环素)的测定。ACQUITY UPLC BEH C8 和 ACQUITY CSH C18 柱分别用于 FL 和 MS 检测,均填充 1.7μm 颗粒。CSH(带电表面技术)填料的混合模式分离机制在分析具有问题两性结构的 TCs 时特别有用。FL 方法基于四环素与钙离子螯合在柱上进行衍生化。在验证参数方面对两种方法进行了比较,包括线性、灵敏度、精密度和准确度。FL 检测的线性范围为 7ngmL(-1)至 50μgmL(-1),大多数分析物的方法检测限(MLOD)低至 0.2ngmL(-1)。MS 检测的灵敏度更高,达到 0.003ngmL(-1)的 MLOD,这是迄今为止分析 TCs 中灵敏度最高的。0.01-50ngmL(-1)范围内的基质匹配校准曲线用于定量,以补偿基质效应,相关系数证明具有良好的线性(0.9940-0.9999)。抗生素从地表水中的提取采用 Oasis HLB 小柱固相萃取法进行。FL 和 MS 检测的准确度分别表示为回收率,范围分别为 96.52%至 127.30%和 91.66%至 123.70%。