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首页> 外文期刊>Molecules >Simultaneous Determination of Pharmaceuticals by Solid-phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry: A Case Study from Sharjah Sewage Treatment Plant
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Simultaneous Determination of Pharmaceuticals by Solid-phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry: A Case Study from Sharjah Sewage Treatment Plant

机译:固相萃取-液相色谱-串联质谱法同时测定药物:以沙迦污水处理厂为例

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The present work describes the optimization and validation of a highly selective and sensitive analytical method using solid phase extraction and liquid chromatography tandem mass spectrometry (SPE LC-MS/MS) for the determination of some frequently prescribed pharmaceuticals in urban wastewater received and treated by Sharjah sewage treatment plant (STP). The extraction efficiency of different SPE cartridges was tested and the simultaneous extraction of pharmaceuticals was successfully accomplished using hydrophilic-lipophilic-balanced reversed phase Waters Oasis HLB cartridge (200 mg/ 6 mL) at pH 3. The analytes were separated on an Aquity BEH C18 column (1.7 μm, 2.1 mm 150 mm) using gradient elution and mass spectrometric analysis were performed in multiple reactions monitoring (MRM) selecting two precursor ions to produce ion transition for each pharmaceutical using positive electrospray ionization (+ESI) mode. The correlation coefficient values in the linear calibration plot for each target compound exceeded 0.99 and the recovery percentages of the investigated pharmaceuticals were more than 84%. Limit of detection (LOD) varied between 0.1-1.5 ng/L and limit of quantification (LOQ) was 0.3-5 ng/L for all analytes. The precision of the method was calculated as the relative standard deviation (RSD%) of replicate measurements and was found to be in the ranges of 2.2% to 7.7% and 2.2% to 8.6% for inter and intra-day analysis, respectively. All of the obtained validation parameters satisfied the requirements and guidelines of analytical method validation.
机译:本工作描述了使用固相萃取和液相色谱串联质谱(SPE LC-MS / MS)的高选择性和灵敏分析方法的优化和验证,该方法用于确定由沙迦接收和处理的城市废水中的某些常用处方药污水处理厂(STP)。测试了不同SPE柱的萃取效率,并使用亲水-亲脂平衡的反相Waters Oasis HLB柱(200 mg / 6 mL)在pH 3下成功完成了药物的同时萃取。在Aquity BEH C18上分离分析物在多反应监测(MRM)中进行梯度洗脱和质谱分析(1.7 µm,2.1 mm×150 mm),选择两种前体离子,以正电喷雾电离(+ ESI)模式为每种药物产生离子跃迁。每种目标化合物的线性校准图中的相关系数值均超过0.99,所研究药物的回收率超过84%。所有分析物的检出限(LOD)在0.1-1.5 ng / L之间,定量限(LOQ)为0.3-5 ng / L。方法的精确度计算为重复测量的相对标准偏差(RSD%),发现日间和日间分析的精度分别在2.2%至7.7%和2.2%至8.6%的范围内。所有获得的验证参数均满足分析方法验证的要求和准则。

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