首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Single-run ultra-high performance liquid chromatography for quantitative determination of ultra-traces of ten popular active pharmaceutical ingredients by quadrupole time-of-flight mass spectrometry after offline preconcentration by solid phase extraction from drinking and river waters as well as treated wastewater
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Single-run ultra-high performance liquid chromatography for quantitative determination of ultra-traces of ten popular active pharmaceutical ingredients by quadrupole time-of-flight mass spectrometry after offline preconcentration by solid phase extraction from drinking and river waters as well as treated wastewater

机译:单次超高效液相色谱法测定十四次普遍的活性药物成分的超痕量,通过饮用河水和河水的固相萃取在离线预浓缩之后的飞行时间谱法以及处理的废水

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摘要

A fit-to-purpose ultra-high performance liquid chromatographic high resolution mass spectrometric method was developed for the ultra-trace analysis of 10 active pharmaceutical ingredients in one chromatographic run as follows: atorvastatin, carbamazepine (CARB), ciprofloxacin (CIPR), clarithromycin (CZAR), diclofenac (DICL), metoprolol (METO), naproxen (NAPA), sitagliptin (SITA), sulfamethoxazole (SULF) and tetracycline. By applying Oasis HLB solid phase extraction cartridges, a 1250-fold enrichment was achieved. For quantitative determination, intemal standard calibration was applied. Lower limits of quantification for the analytes were <= 0.025 mu g/L. Good linearity was found between 0.01 and 5 mu g/L in most cases. Generally, overall recovery for drinking, river and treated wastewater samples spiked with the target analytes at one concentration level comparable with the blank values and another one by one order of magnitude higher was between 80 and 120%. The relative standard deviation values were <= 16%. The proposed method has been applied for the aforementioned water matrices sampled monthly between January and March 2019. Concentration of GARB in drinking water per se was about 0.025 mu g/L, confirming the low removal rates during river bank filtration applied for drinking water production. Seven compounds were present in the river water in <= 50 ng/L. Eight compounds were detected at least once from the treated wastewater samples including CARB, DICL, NAPR and SITA in > 1 mu g/L. Concentration of CARB, DICL, METO, SITA used for chronic affections was almost constant during the monitored time period. To the contrary, concentration of CIPR, CLAR, SULF used for acute infections registered peak values in the same samples taken in winter.
机译:开发了适合的超高效液相色谱高分辨率质谱法,用于在一种色谱中进行10个活性药物成分的超痕量分析,如下所示:阿托伐他汀,卡巴马啶(CARB),CiProfloxacin(CIPR),Clarithromycin (Czar),双氯芬酸(DIC1),美容托洛尔(METO),萘普生(NAPA),SITAGLIPTIN(SITA),磺胺甲恶唑(SULF)和四环素。通过施加绿洲HLB固相萃取盒,实现了1250倍的富集。为了定量测定,应用了内部标准校准。分析物的较低量化限制为<=0.025μg/ L.在大多数情况下,在0.01和5μg/ l之间发现了良好的线性。通常,饮用的总体恢复,河流和处理的废水样品在一个浓度水平上与靶分析物一起掺入,其浓度水平与空白值相当,另一个量级高于80%至120%。相对标准偏差值<= 16%。所提出的方法已应用于2019年1月至3月期间每月采样的上述水矩阵。饮用水中的服装浓度为约0.025μg/ L,确认河流过滤期间的较低的去除率施用用于饮用水生产。河水中存在七种化合物<= 50 ng / L.从包括Carb,DiCl,NaPR和SITA的处理过的废水样品中至少检测到八种化合物,包括氨基,DIC1,NAPR和SITA>1μg/ L.在监测时间段内,用于慢性浓厚的慢性浓厚的慢性浓度的碱度浓度几乎是恒定的。相反,CIPR,Clar,Sulf用于急性感染的急性感染,在冬季采集的相同样品中注册峰值。

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