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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:通过固相萃取和液相色谱 - 串联质谱法同时测定药物 - Sharjah污水处理厂的案例研究

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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 (R) Oasis HLB cartridge (200 mg/ 6 mL) at pH 3. The analytes were separated on an Aquity BEH C18 column (1.7 mu m, 2.1 mm x 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:本作本作者描述了使用固相提取和液相色谱串联质谱(SPE LC-MS / MS)进行高选择性和敏感的分析方法的优化和验证,用于测定由沙迦接受和治疗的城市废水中的一些经常规定的药品污水处理厂(STP)。测试了不同SPE盒的提取效率,并在pH3的pH 3下使用亲水性 - 亲脂性 - 平衡的反相水(R)Oasis HLB盒(200mg / 6ml)成功地完成了药物的同时提取。分析物在一个在多重反应监测(MRM)中,使用阳性电喷雾电离(+ ESI),在多重反应监测(MRM)中进行使用梯度洗脱和质谱分析来进行使用梯度洗脱和质谱分析来进行使用梯度洗脱和质谱分析的C18柱(1.7μm,2.1mm×150mm),以产生每种药物的离子转变(+ esi)模式。每个目标化合物的线性校准图中的相关系数值超过0.99,并将研究的药物的回收百分比大于84%。检测极限(LOD)在0.1-1.5 ng / L之间变化,并且所有分析物的定量限制为0.3-5 ng / L.该方法的精度计算为复制测量的相对标准偏差(RSD%),并且发现其范围为2.2%至7.7%和2.2%至8.6%,分别为间分析。所有获得的验证参数都满足了分析方法验证的要求和指导。

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