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

被引:27
作者
Semreen, Mohammad H. [1 ,2 ]
Shanableh, Abdallah [3 ]
Semerjian, Lucy [4 ]
Alniss, Hasan [1 ,2 ]
Mousa, Mouath [3 ]
Bai, Xuelian [5 ]
Acharya, Kumud [5 ]
机构
[1] Univ Sharjah, Coll Pharm, POB 27272, Sharjah, U Arab Emirates
[2] Univ Sharjah, Sharjah Inst Med Res, POB 27272, Sharjah, U Arab Emirates
[3] Univ Sharjah, Res Inst Sci & Engn, POB 27272, Sharjah, U Arab Emirates
[4] Univ Sharjah, Coll Hlth Sci, POB 27272, Sharjah, U Arab Emirates
[5] Desert Res Inst, 755 E Flamingo Rd, Las Vegas, NV 89119 USA
来源
MOLECULES | 2019年 / 24卷 / 03期
关键词
liquid chromatography-tandem mass spectrometry; pharmaceuticals; wastewater analysis; solid phase extraction; WASTE-WATER TREATMENT; PERSONAL-CARE PRODUCTS; ENDOCRINE DISRUPTING COMPOUNDS; ENVIRONMENTAL RISK; GAS-CHROMATOGRAPHY; REMOVAL; ANTIBIOTICS; HORMONES; FATE; SAMPLES;
D O I
10.3390/molecules24030633
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:16
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