欢迎来到《四川大学学报(医学版)》

功能化聚丙烯腈纳米纤维膜高通量检测水源水中多种类抗生素

High-Throughput Detection of Multiple Classes of Antibiotics in Source Water Using a Functionalized Polyacrylonitrile Nanofiber Membrane

  • 摘要:
    目的 开发一种新固相萃取(solid-phase extraction, SPE)方法用于实现水源水中结构多样、性质差异显著的多种抗生素的高效共萃取,结合超高效液相色谱-串联质谱(ultra-performance liquid chromatography-tandem mass spectrometry, UPLC-MS/MS)技术建立水源水中多种抗生素高通量检测的新方法。
    方法 通过混合静电纺丝法和多巴胺氧化自聚合反应制备了聚多巴胺与富马酸-锆金属有机骨架材料〔zirconium (Ⅳ) fumarate metal-organic frameworks, MOF-801〕双重修饰的聚丙烯腈纳米纤维膜(PDA@PAN/MOF-801 NFMs)作为SPE吸附剂,优化SPE和UPLC-MS/MS的关键参数,并应用于苏州市14个集中式饮用水的水源水中的抗生素污染检测以考查方法的实际应用潜力。
    结果 PDA@PAN/MOF-801 NFMs通过协同静电作用、氢键作用和π-π相互作用等多种保留机制,实现了6类32种抗生素的同时高效吸附。基于此建立的SPE方法结合UPLC-MS/MS可实现水源水中多种抗生素高通量检测,方法检出限为0.001~0.05 ng/L,定量限为0.005~500 ng/L;加标回收率为70.14%~111.50%;日内精密度<14.12%,日间精密度<15.07%,具有良好的灵敏度、准确度和精密度。
    结论 本研究成功开发了一种基于新型纳米纤维膜吸附剂的高效分析方法,为环境水体中多种抗生素高通量检测提供了新的技术参考,并具有一定的实际应用潜力。

     

    Abstract:
    Objective To develop a novel solid-phase extraction (SPE) method based on a functionalized nanofiber membrane for the efficient co-extraction of structurally diverse antibiotics with markedly different physicochemical properties from source water, and to establish a high-throughput analysis method by coupling this technique with ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
    Methods A polydopamine and zirconium (Ⅳ) fumarate metal-organic frameworks (MOF-801) co-modified polyacrylonitrile nanofiber membrane (PDA@PAN/MOF-801 NFMs) was prepared as the SPE adsorbent through hybrid electrospinning and dopamine self-polymerization. Critical SPE and UPLC-MS/MS parameters were optimized, and the method was applied to analyze antibiotic contamination in source water samples from 14 sources of centralized drinking water supply in Suzhou, China, to evaluate the practical application potential of the method.
    Results The PDA@PAN/MOF-801 NFMs adsorbent demonstrated efficient adsorption of 32 antibiotics from 6 classes through multiple retention mechanisms, including synergistic electrostatic interactions, hydrogen bonding, and π-π interactions. In combination with UPLC-MS/MS, the SPE method we developed enabled high-throughput detection of multiple antibiotics in source water, with limits of detection (LOD) being 0.001-0.05 ng/L and limits of quantitation (LOQ) being 0.005-500 ng/L. Spiked recoveries were 70.14%-111.50%. Intra-day relative standard deviation (RSD) was below 14.12% and the inter-day RSD was below 15.07%. The method demonstrated excellent sensitivity, accuracy, and precision.
    Conclusion In this study, we successfully developed an efficient analytical method based on a novel nanofiber membrane adsorbent. This approach provides a new technical reference for the high-throughput detection of multiple antibiotics in environmental waters and shows promising potential for practical applications.

     

/

返回文章
返回