色谱 ›› 2022, Vol. 40 ›› Issue (4): 323-332.DOI: 10.3724/SP.J.1123.2021.07014

• 研究论文 • 上一篇    下一篇

基于金属有机骨架复合气凝胶的分散固相萃取-超高效液相色谱-串联质谱法测定水中5种非甾体类抗炎药

凌慧娟1, 吴阁格1,*(), 李爽1, 周乾2, 李春欣2, 马继平1,*()   

  1. 1.青岛理工大学环境与市政工程学院, 山东 青岛 266033
    2.光大青岛理工环境技术研究院, 山东 青岛 266033
  • 收稿日期:2021-07-26 出版日期:2022-04-08 发布日期:2022-04-01
  • 通讯作者: 吴阁格,马继平
  • 基金资助:
    国家自然科学基金(21976099);山东省自然科学基金(ZR2019MB046)

Determination of five nonsteroidal anti-inflammatory drugs in water by dispersive solid phase extraction-ultra performance liquid chromatography-tandem mass spectrometry based on metal-organic framework composite aerogel

LING Huijuan1, WU Gege1,*(), LI Shuang1, ZHOU Qian2, LI Chunxin2, MA Jiping1,*()   

  1. 1. School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266033, China
    2. Everbright Qingdao Institute of Environmental Technology, Qingdao 266033, China
  • Received:2021-07-26 Online:2022-04-08 Published:2022-04-01
  • Contact: WU Gege, MA Jiping
  • Supported by:
    National Natural Science Foundation of China(21976099);Natural Science Foundation of Shandong Province of China(ZR2019MB046)

摘要:

非甾体类抗炎药(NSAIDs)能在环境水体中长期稳定存在,不仅对生物有慢性毒性还能增加病原体的耐药性,开发可靠的测定水样中痕量非甾体抗炎药的分析方法至关重要。该文制备新型金属有机骨架/壳聚糖复合气凝胶材料Co-UiO-67(bpy)/CS分散固相萃取吸附剂,将其用于环境水体中酮洛芬、萘普生、氟比洛芬、双氯芬酸、布洛芬5种非甾体类抗炎药的富集,结合超高效液相色谱-串联质谱法(UPLC-MS/MS),建立了基于金属有机骨架材料(MOFs)复合气凝胶环境水体中药物残留检测的新方法。为获得最佳的萃取效率,对影响萃取效果的主要因素(材料类型、MOFs用量、萃取时间、水样pH值、离子强度、甲酸体积分数、洗脱时间、洗脱剂体积)进行条件考察及优化。优化结果显示,吸附剂5 min内就可实现目标化合物的完全吸附,用总体积为5 mL的1%甲酸甲醇溶液洗脱6 min,目标化合物就能充分解吸。在最优的固相萃取条件下建立分析方法,结果表明,5种非甾体类抗炎药在各自范围内线性关系良好,线性相关系数均大于0.9937,方法的检出限(LOD)和定量限(LOQ)分别为0.32~2.06 ng/L和1.05~6.78 ng/L。在40、250和1500 ng/L 3个加标水平下进行加标回收试验,5种待测物的平均回收率为74.5%~114.1%。日内、日间相对标准偏差分别为1.3%~12.3%和1.3%~11.5%。将该方法用于实际水样的检测,市政污水检测出微量的酮洛芬和氟比洛芬,含量分别为14.52 ng/L和10.05 ng/L。该方法具有良好的灵敏度、准确度和精密度,操作简便,耗时短,为环境水体中痕量非甾体抗炎药富集检测提供了新方法。

关键词: 超高效液相色谱-串联质谱, 分散固相萃取, 金属有机骨架, 复合气凝胶, 非甾体抗炎药, 环境水体

Abstract:

Nonsteroidal anti-inflammatory drugs (NSAIDs) are a class of synthetic drugs that do not contain glucocorticoids. NSAIDs are widely used for their analgesic, antipyretic, and anti-inflammatory effects. Due to their low adsorption coefficients and recalcitrance to biodegradation, NSAIDs readily enter environmental water through sewage discharge and exist stably for long periods. The long-term presence of trace amounts of NSAIDs in environmental water has adverse health effects on humans and animals. Therefore, it is important to establish an appropriately sensitive and reliable method for the determination of NSAIDs in environmental water, where their concentrations are low. Ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) is highly selective and sensitive, and so is especially suitable for detection of NSAIDs. Solid phase extraction is one of the most commonly used pretreatment methods. The extraction efficiency depends mainly on the adsorbents used. Metal-organic framework (MOF) aerogel SPE materials combine the attributes of highly selective adsorption property and high affinity. Moreover, the monolithic structure of the MOF aerogel composite simplifies the solid-liquid separation process. In this work, a novel MOF/chitosan (CS) composite designated Co-UiO-67(bpy)/CS, was prepared as the adsorbent material to enrich ketoprofen (KPF), naproxen (NPX), flurbiprofen (FPN), diclofenac (DCF), and ibuprofen (IBF) in water. This facilitated the detection of these compounds by UPLC-MS/MS. Co-UiO-67(bpy) was synthesized by a solvothermal method by mixing zirconium chloride, cobalt chloride, and the organic ligand 2,2-bipyridine-5,5 dicarboxylic acid. A CS suspension was used to prepared the hydrogel, which was freeze-dried to obtain the Co-UiO-67(bpy)/CS aerogel. The prepared material was characterized by Fourier transform-infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). Co-UiO-67 (bpy) was embedded into chitosan. A layered porous MOF composite aerogel was observed. The extraction efficiency of the five NSAIDs was investigated and optimized by assessing type of extraction material, MOF amount, extraction time, sample pH, ionic strength, formic acid concentration in eluent, elution time, and elution volume. The optimized results showed that the target compounds could be completely adsorbed within 5 min. In the UPLC-MS/MS experiment, NSAIDs were analyzed in the negative ionization multiple radiation monitoring (MRM) mode. Gradient elution was carried out with 0.01% formic acid aqueous solution and methanol as the mobile phases. The analytical method was established in the optimized extraction conditions. The five NSAIDs displayed good linearity with linear correlation coefficients greater than 0.9937. The limits of detection (LODs) and limits of quantification (LOQs) of this developed method were 0.32-2.06 ng/L and 1.05-6.78 ng/L, respectively. Satisfactory recoveries of the five analytes were achieved within 74.5%-114.1% at three spiked concentrations of 40, 250, and 1500 ng/L, as well as good precision with relative standard deviations of 1.3%-12.3% (intra-day) and 1.3%-11.5% (inter-day). The method was then used to test real-world water samples. Trace amounts of ketoprofen and flurbiprofen were detected in municipal wastewater (14.52 ng/L and 10.05 ng/L, respectively). The method exhibited good sensitivity, accuracy, and precision, and the operation process was convenient. The present study thus presents a novel method for the detection of the trace NSAIDs in environmental waters.

Key words: ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), dispersive solid phase extraction (DSPE), metal-organic frameworks (MOFs), composite aerogel, nonsteroidal anti-inflammatory drugs (NSAIDs), environmental waters

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