Departamento de Medio Ambiente, INIA, Carretera de A Coruña km 7, 28040, Madrid, Spain.
Departamento de Medio Ambiente, INIA, Carretera de A Coruña km 7, 28040, Madrid, Spain.
J Chromatogr A. 2019 Feb 22;1587:42-49. doi: 10.1016/j.chroma.2018.12.015. Epub 2018 Dec 10.
In the present work, the preparation of a new selective molecularly imprinted polymer (MIP) for the family of fluoroquinolones (FQs) in the pores of polypropylene hollow fibers (HFs) is proposed. The resulting MIP-HFs, which combine solid-phase microextraction (SPME) and molecular imprinting technologies, were used to develop a selective microextraction methodology (MIP-HFM) to determine selected FQs danofloxacin, norfloxacin, enrofloxacin and ciprofloxacin in real samples of environmental and biological interest. Measurements during the optimization of the MIP-HFM and its application to the analyses of real samples were performed by HPLC-UV and HPLC-MS/MS. In order to establish optimum rebinding conditions, the effect of key experimental parameters such as loading media, extraction time and stirring-rate were studied. The developed MIP composites exhibited recognition properties towards the selected hydrophilic antibiotics in non-polar media (toluene) and in polar protic systems such as methanol and methanol/water solutions, up to 20% water content. Recoveries by the developed method for all FQs tested in surface water, groundwater and urine spiked with the analytes of interest at two different concentration levels were within 9.4-24.5 %, with a relative standard deviation, generally <20% (n = 3). The detection limits were within 0.1-10 μg L, depending upon the antibiotic and the type of sample.
在本工作中,提出了在聚丙烯中空纤维(HF)的孔中制备用于氟喹诺酮类(FQs)家族的新型选择性分子印迹聚合物(MIP)。所得的 MIP-HF 结合固相微萃取(SPME)和分子印迹技术,用于开发选择性微萃取方法(MIP-HFM),以在环境和生物相关实际样品中测定选定的 FQs 丹诺氟沙星、诺氟沙星、恩诺沙星和环丙沙星。在 MIP-HFM 的优化和对实际样品的分析中的测量是通过 HPLC-UV 和 HPLC-MS/MS 进行的。为了建立最佳的再结合条件,研究了加载介质、萃取时间和搅拌速率等关键实验参数的影响。所开发的 MIP 复合材料在非极性介质(甲苯)和极性质子体系(甲醇和甲醇/水溶液)中表现出对所选亲水性抗生素的识别性能,最高可达 20%的水含量。在所测试的所有 FQs 的地表水、地下水和尿液中,通过所开发的方法进行的回收率,在两种不同浓度水平下,加标目标分析物的回收率在 9.4-24.5%之间,相对标准偏差通常<20%(n=3)。检测限在 0.1-10μg L 之间,取决于抗生素和样品的类型。