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1.
J AOAC Int ; 104(1): 91-97, 2021 Mar 05.
Article in English | MEDLINE | ID: mdl-33751070

ABSTRACT

BACKGROUND: Determination of emerging pollutants including pharmaceuticals, pesticides, industrial chemicals and hormones in different environmental samples is very important for human health. OBJECTIVE: Experimental design enabled parameters to be evaluated for their effects onextraction output as well as their interactive effects. METHOD: A multivariate experimental design was used to attain optimum conditions of a dispersive liquid-liquid microextraction method for preconcentration of pesticides and pharmaceuticals for determination by GC-MS. RESULTS: The optimum parameters suggested by the design model were 200 µL of chloroform, 1.96 mL of ethanol, and 40 s vortexing period. LOD and LOQ were calculated using linear calibration plots of the analytes developed in the standard concentration range of 2.0 µg/L-2.0 mg/L. CONCLUSIONS: Enhancement in detection power of the analytes recorded by the optimized method with respect to direct GC-MS determination (based on LOD values) was in the range of 3.6 and 539 folds. Spiked recovery experiments for municipal, medical, and synthetic wastewater samples yielded low recovery results when calculated against aqueous standard solutions. Matrix matched calibration standards were used to mitigate interferences from the waste samples and the percent recoveries obtained were close to 100%. This established accuracy and applicability of the developed method. HIGHLIGHTS: The detection limits were found between 0.50 ng/mL and 37 ng/mL. An accurate, simple and sensitive analytical method was developed for the analytes.


Subject(s)
Liquid Phase Microextraction , Pesticides , Water Pollutants, Chemical , Citalopram , Gas Chromatography-Mass Spectrometry , Haloperidol , Humans , Limit of Detection , Olanzapine , Pesticides/analysis , Wastewater/analysis , Water Pollutants, Chemical/analysis
2.
Environ Toxicol Chem ; 40(6): 1570-1575, 2021 06.
Article in English | MEDLINE | ID: mdl-33651385

ABSTRACT

Pharmaceutical products are widely consumed globally and are commonly found in wastewaters as a result of constant excretion and disposal into sewers. The present study proposes an efficient binary solvent dispersive liquid-liquid microextraction (BS-DLLME) method that was developed for preconcentration of 7 nervous system drug active compounds from aqueous media for their determination at trace levels by gas chromatography-mass spectrometry. The drug analytes included 3 antidepressants, 2 antipsychotics, 1 antiepileptic, and 1 antidementia. Optimum conditions of the BS-DLLME method were acquired by univariate optimization of parameters including type of binary solvents, ratio of binary solvents, type of disperser solvent, volume of binary solvents, and volume of disperser solvent. Detection and quantification limits were calculated in the range of 0.28 to 6.5 µg/L. Municipal wastewater, medical wastewater, synthetic domestic wastewater, and lake water were utilized as real samples in spike recovery experiments; and the results (94-106%) indicated the method's applicability and accuracy at quantifying the analytes in complex matrices. Environ Toxicol Chem 2021;40:1570-1575. © 2021 SETAC.


Subject(s)
Liquid Phase Microextraction , Water Pollutants, Chemical , Gas Chromatography-Mass Spectrometry/methods , Limit of Detection , Liquid Phase Microextraction/methods , Nervous System , Solvents/chemistry , Water , Water Pollutants, Chemical/analysis
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