Determination of antibiotics of the tetracycline group in water by high-performance liquid chromatography on a diode matrix detector with preliminary concentration by solid-phase extraction

Larisa P. Nekrasova, Oksana Ju. Kuleshova
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Abstract

Introduction. Antibiotic contamination of the environment is a serious environmental threat that poses a hazard to human health. To monitor the content of tetracycline antibiotics in environmental objects and control technological processes aimed at their disposal, accessible analytical methods are needed. Purpose of the study. Development of a method for determining antibiotics of the tetracycline group in water using a diode array detector with preliminary solid-phase concentration. Material and methods. The objects of the study were model solutions of minocycline, tetracycline, oxytetracycline, demeclocycline, metacycline, and doxycycline in deionized, tap, natural, and treated wastewater. For solid-phase extraction, Diapak P and Diapak PG cartridges were used. SPE was performed using a VacMaster-10 manifold (Biotage). Chromatographic separation was carried out on Diasphere C10CN and Kromasil Eternity 250 × 4.6 mm 5 µm columns on an Agilent 1100 liquid chromatograph (Agilent Technology). Results. Optimal conditions for the chromatographic separation of minocycline, tetracycline, oxytetracycline, demeclocycline, metacycline, and doxycycline were selected: isocratic mode, wavelength of 350 nm, mobile phase – acetonitrile: aqueous solution of phosphoric acid (pH = 3.0). The analysis time on Diasphere C10CN and Kromasil Eternity columns was 12 and 14 minutes, respectively. The reliability of the linear approximation in both cases was more than 0.99, however, the slopes on the Kromasil Eternity column were 1.35 –1.65 times higher than on Diasphere C10CN. The degree of extraction of tetracyclines from deionized water on Diapak P and Diapak PG cartridges was 90–95%, from tap water 61–89%, from purified waste water: 51–87%. Limitations. The method is not suitable for water bodies with tetracycline contents less than 2 µg/dm3. Conclusion. An HPLC method has been developed for the determination of minocycline, tetracycline, oxytetracycline, demeclocycline, metacycline, and doxycycline in water with preliminary SPE concentration on Diapak P and Diapak PG cartridges. The lower limit of determination for the sorption of target compounds from 0,1 dm3 of sample was 2 μg/dm3.
采用二极管矩阵检测器上的高效液相色谱法和固相萃取初步浓缩法测定水中的四环素类抗生素
导言。环境中的抗生素污染是一种严重的环境威胁,对人类健康造成危害。为了监测环境物体中四环素类抗生素的含量,并控制处理这些抗生素的技术过程,需要有简便易行的分析方法。研究目的开发一种利用二极管阵列检测器初步固相浓缩法测定水中四环素类抗生素含量的方法。材料和方法。研究对象是去离子水、自来水、天然废水和处理过的废水中的米诺环素、四环素、土霉素、地美环素、甲氧环素和强力霉素的模型溶液。固相萃取使用的是 Diapak P 和 Diapak PG 滤芯。固相萃取使用的是 VacMaster-10 歧管(Biotage)。色谱分离采用安捷伦 1100 型液相色谱仪(安捷伦科技公司)上的 Diasphere C10CN 和 Kromasil Eternity 250 × 4.6 mm 5 µm 色谱柱。结果选择了米诺环素、四环素、土霉素、地美环素、甲氧环素和强力霉素色谱分离的最佳条件:等度模式,波长 350 nm,流动相 - 乙腈:磷酸水溶液(pH = 3.0)。Diasphere C10CN 和 Kromasil Eternity 色谱柱的分析时间分别为 12 分钟和 14 分钟。两种色谱柱的线性近似可靠性均大于 0.99,但 Kromasil Eternity 色谱柱的斜率是 Diasphere C10CN 色谱柱的 1.35-1.65 倍。Diapak P 和 Diapak PG 滤芯对去离子水中四环素的萃取率为 90-95%,对自来水的萃取率为 61-89%,对净化废水的萃取率为 51-87%:51-87%.局限性。该方法不适用于四环素含量低于 2 µg/dm3 的水体。结论。通过在 Diapak P 和 Diapak PG 色谱柱上进行初步固相萃取浓缩,建立了测定水中米诺环素、四环素、土霉素、地美环素、甲氧环素和强力霉素的高效液相色谱法。0.1 dm3 样品中目标化合物的吸附测定下限为 2 μg/dm3。
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