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Ultra performance liquid chromatography tandem mass spectrometry performance evaluation for analysis of antibiotics in natural waters

机译:天然水中抗生素分析的超高效液相色谱串联质谱性能评估

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An ultra performance liquid chromatography electrospray tandem mass spectrometry (UPLC/MS/MS) method was developed and validated for the determination of 17 antibiotics in natural waters in one single extraction and chromatographic procedure. Gradient separation conditions were optimised for 17 compounds belonging to five different antibiotic groups: quinolones (oxolinic acid, nalidixic acid, pipemidic acid, flumequine), fluoroquinolones (enoxacin, ciprofloxacin, norfloxacin, ofloxacin, enrofloxacin, sarafloxacin, danofloxacin, difloxacin, lomefloxacin), sulphonamides (sulphamethoxazole, sulphamethazine), nitro-imidazole (ornidazole) and diaminopyrimidine (trimethoprim). The separation of all compounds, obtained using a 1.7 μm particle size column (100 mm × 2.1 mm), was achieved within 10 min time. Water samples were adjusted to pH 7 and extracted using Oasis hydrophilic–lipophilic balance (HLB) solid phase extraction cartridges. After elution with methanol and concentration, extracts were injected in a C18 column (Acquity UPLC BEH C18) and detected by tandem mass spectrometry. Average recovery from 100 ng L?1 fortified samples was higher than 70% for most of the compounds, with relative standard deviations below 20%. Performances of the method (recoveries, detection limit, quantification limit and relative standard deviation) and matrix effects were studied, and results obtained showed that method was suitable for routine analysis of antibiotics in surface water. Samples analysis from Seine River (France) confirmed the interest of antibiotic contamination evaluation in that area.
机译:开发了一种超高效液相色谱电喷雾串联质谱(UPLC / MS / MS)方法,并通过一次萃取和色谱法验证了该方法可用于测定天然水中的17种抗生素。对属于五个不同抗生素组的17种化合物的梯度分离条件进行了优化:喹诺酮类(草酸,萘啶酮酸,哌啶酸,氟丁喹),氟喹诺酮类药物(依诺沙星,环丙沙星,诺氟沙星,氧氟沙星,恩氟沙星,赛拉沙星,二氧氟沙星,双氧氟沙星)磺酰胺(磺胺甲恶唑,磺胺二甲嘧啶),硝基咪唑(甲硝唑)和二氨基嘧啶(甲氧苄啶)。使用1.7μm粒径色谱柱(100 mm×2.1 mm)分离的所有化合物均在10分钟内完成分离。将水样品的pH调节至7,然后使用Oasis亲水亲脂平衡(HLB)固相萃取柱进行萃取。用甲醇洗脱并浓缩后,将提取物注入C18柱(Acquity UPLC BEH C18)中,并通过串联质谱法进行检测。大多数化合物从100 ng L?1 强化样品中的平均回收率均高于70%,相对标准偏差低于20%。研究了该方法的性能(回收率,检出限,定量限和相对标准偏差)和基质效应,所得结果表明该方法适用于地表水中抗生素的常规分析。来自法国塞纳河的样品分析证实了对该地区抗生素污染评估的兴趣。

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