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UPLC-MS/MS screening method for simultaneous identification and characterisation of acidic and basic Pharmaceuticals

机译:UPLC-MS / MS筛选方法可同时鉴定和表征酸性和碱性药物

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摘要

A new screening method was developed for the simultaneous determination of seven acidic and basic pharmaceuticals by the ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) utilising triple quadrupole mass spectrometry as a detector. The target pharmaceutical compounds of interest in this work belong to different classes of pharmaceutical group with different physico-chemical properties. Both the positive and negative ionisation modes (dual ionisation mode) in electrospray ionisation (ESI) were used simultaneously. Unlike previous studies, the performance of the dual ionisation mode was compared with the positive and negative ionisation modes individually in terms of analysis time and sensitivity. Results indicate that the developed screening method was successfully applied for the simultaneous determination of the acidic and basic pharmaceutical compounds. Using dual ionisation mode reduced the analyses time while still maintaining sensitivity and quality of the analytical result. The new method was implemented in detecting the targeted analyte in a real sample of wastewater. The instrument detection limit (IDL) was as low as 9.7 fg, indicating a high sensitivity as compared to the corresponding methods. The precision of the instrument was calculated as the relative standard deviation (RSD) ranging from 1.4 to 11.0%. The limit of quantification (LOQ) for the method was over the range 0.77-177 ng L-1 and 1.05-100 ng L-1 for the influent and effluent wastewater, respectively.
机译:通过使用三重四极杆质谱作为检测器的超高效液相色谱-串联质谱法(UPLC-MS / MS),开发了一种同时测定7种酸性和碱性药物的新筛选方法。在这项工作中目标药物目标化合物属于具有不同理化性质的不同类别的药物组。同时使用电喷雾电离(ESI)中的正电离和负电离模式(双重电离模式)。与以前的研究不同,在分析时间和灵敏度上分别将双重电离模式的性能与正电离模式和负电离模式进行了比较。结果表明,开发的筛选方法已成功应用于酸性和碱性药物化合物的同时测定。使用双重电离模式可减少分析时间,同时仍保持分析结果的灵敏度和质量。实施了该新方法以检测实际废水样品中的目标分析物。仪器检测限(IDL)低至9.7 fg,表明与相应方法相比灵敏度高。仪器的精度计算为相对标准偏差(RSD),范围为1.4至11.0%。对于进水和出水废水,该方法的定量限(LOQ)分别在0.77-177 ng L-1和1.05-100 ng L-1范围内。

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