School of Chemistry, College of Science, University of Tehran, Tehran, Iran.
J Sci Food Agric. 2021 Apr;101(6):2304-2311. doi: 10.1002/jsfa.10851. Epub 2020 Oct 17.
Tetracycline antibiotics are employed for human and animal health and for speeding up growth rates. However, their presence in food products and environmental waters has been a concern for some years. Therefore, a variety of sample preparation methods have been developed for the analysis of tetracycline residues in these matrices.
An electrochemically controlled solid phase microextraction based on a modified copper electrode with polyaniline/graphene oxide (PANI/GO) conductive nanocomposite was developed for the extraction of oxytetracycline, tetracycline and doxycycline before high-performance liquid chromatography-UV analysis. PANI/GO was synthesized by in situ chemical oxidative polymerization, characterized by scanning electron microscopy and Fourier-transform infrared spectroscopy, and bound on the electrode using high purity conductive double-sided adhesive carbon glue. The significant factors affecting the performance of microextraction were investigated and optimized. Under the optimized conditions [sample, 15 mL; sorbent, 10 mg; pH, 3.0; electroextraction voltage, -0.9 V; electroextraction time, 20 min; eluent (MeOH/NH ), 500 μL; and desorption time, 5 min], the limits of detection for target analytes were in the ranges 0.32-1.01 and 2.42-7.59 μg L in water and milk samples, respectively. The linear ranges were 1.06-750 μg L for water and 8.05-750 μg L for milk samples. The intra-day and inter-day precisions were 2.32-3.80 and 3.29-4.25, respectively. The method was applied to the determination of analytes in milk and water samples with different fat contents, and the recoveries were obtained in the range 71-104%.
The developed electro-microextraction method provides a facile, rapid, cost-effective, sensitive and efficient promising procedure for the extraction of antibiotics in complex matrices. © 2020 Society of Chemical Industry.
四环素类抗生素被广泛应用于人类和动物的健康以及促进生长速度。然而,其在食品和环境水中的存在已经引起了人们多年的关注。因此,人们开发了各种样品制备方法来分析这些基质中的四环素残留。
本文采用电化学控制的固相微萃取方法,以经过修饰的铜电极为基础,结合聚邻苯二胺/氧化石墨烯(PANI/GO)导电纳米复合材料,对高效液相色谱-紫外检测法分析前的土霉素、四环素和强力霉素进行萃取。PANI/GO 通过原位化学氧化聚合合成,采用扫描电子显微镜和傅里叶变换红外光谱进行表征,并通过高纯导电双面胶碳胶结合在电极上。实验考察并优化了影响微萃取性能的显著因素。在优化条件下[样品,15 mL;吸附剂,10 mg;pH 值,3.0;电萃取电压,-0.9 V;电萃取时间,20 min;洗脱液(甲醇/氨),500 μL;解吸时间,5 min],目标分析物在水和牛奶样品中的检测限分别为 0.32-1.01 和 2.42-7.59 μg/L。水和牛奶样品的线性范围分别为 1.06-750 μg/L 和 8.05-750 μg/L。日内和日间精密度分别为 2.32-3.80 和 3.29-4.25。该方法应用于不同脂肪含量的牛奶和水样中分析物的测定,回收率在 71-104%范围内。
所开发的电微萃取方法为复杂基质中抗生素的提取提供了一种简便、快速、经济高效、灵敏且有前景的方法。