Speltini Andrea, Sturini Michela, Maraschi Federica, Viti Simona, Sbarbada Davide, Profumo Antonella
Department of Chemistry, University of Pavia, via Taramelli 12, 27100 Pavia, Italy.
Department of Chemistry, University of Pavia, via Taramelli 12, 27100 Pavia, Italy.
J Chromatogr A. 2015 Sep 4;1410:44-50. doi: 10.1016/j.chroma.2015.07.093. Epub 2015 Jul 29.
A novel, simple and straightforward method for determination of fluoroquinolones (FQs) in compost has been developed. The procedure entails a low-pressurized microwave-assisted extraction (MAE) carried out by a high performance instrument, in alkaline aqueous solution containing magnesium ions as FQs complexing agent, followed by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS). Ciprofloxacin (CIP), Enrofloxacin (ENR), Levofloxacin (LEV) and Norfloxacin (NOR), four widely used FQ antibiotics, were simultaneously extracted from compost by a single MAE cycle (20min, 135°C). The method was validated in terms of linearity, selectivity, sensitivity and accuracy. Quantitative absolute recovery (70-112%, n=3) and suitable precision (RSD<15%, n=3) were observed, at concentration levels ranging from 25 ng g(-1) to 2500 ng g(-1). Analytes were separated in a 10min chromatographic run and quantified/confirmed in single reaction monitoring (SRM) mode. UPLC coupled to SRM-MS detection allowed to achieve improved sensitivity, and selective detection. Method detection and quantification limits, MDLs and MQLs, were in the range 2.2-3.0 ng g(-1) and 6.6-9.0 ng g(-1), respectively. The high-performance microwave system here used strongly improved the extraction efficiency with respect to a conventional apparatus. The procedure proved to be simpler, less expensive, faster, and more green with respect to the few methods currently described in literature, providing at the same time suitable recovery and reproducibility. The analytical method has been applied to the analysis of actual compost samples, wherein FQs have been quantified at concentrations up to 88 ng g(-1).
已开发出一种新颖、简单且直接的方法来测定堆肥中的氟喹诺酮类药物(FQs)。该方法包括在含有镁离子作为FQs络合剂的碱性水溶液中,通过高性能仪器进行低压微波辅助萃取(MAE),随后进行超高效液相色谱串联质谱(UPLC-MS)分析。环丙沙星(CIP)、恩诺沙星(ENR)、左氧氟沙星(LEV)和诺氟沙星(NOR)这四种广泛使用的FQ抗生素,通过单次MAE循环(20分钟,135°C)从堆肥中同时萃取出来。该方法在线性、选择性、灵敏度和准确性方面得到了验证。在浓度范围为25 ng g⁻¹至2500 ng g⁻¹时,观察到定量绝对回收率为70 - 112%(n = 3),精密度良好(RSD < 15%,n = 3)。分析物在10分钟的色谱运行中分离,并在单反应监测(SRM)模式下进行定量/确认。UPLC与SRM-MS检测相结合,提高了灵敏度和选择性检测能力。方法检测限和定量限,即MDLs和MQLs,分别在2.2 - 3.0 ng g⁻¹和6.6 - 9.0 ng g⁻¹范围内。与传统仪器相比,这里使用的高性能微波系统极大地提高了萃取效率。相对于目前文献中描述的少数方法,该方法被证明更简单、成本更低、速度更快且更环保,同时具有合适的回收率和重现性。该分析方法已应用于实际堆肥样品的分析,其中FQs的定量浓度高达88 ng g⁻¹。