Abstract

Independent methods for determination of organic contaminants such as pharmaceuticals and pesticides in drinking water samples, using SPE as the extraction technique and LC–MS/MS in the MRM mode with electrospray ionization, were developed and validated. Different SPE sorbents were evaluated, including lab-made fluorinated and phenyl and commercial Oasis HLB and C18, with the commercial phases being more suitable for the target compounds. Recoveries in the range of 70–120% were obtained for all target compounds, with the exception for paracetamol (acetaminophen), and precision values (inter-day and intra-day), expressed in terms of relative standard deviations (RSD), lower than 20% were obtained for all target compounds. Quantification limits were in the range of 0.006–0.208μgL−1 and the methods developed were successfully applied for the analysis of drinking water samples, detecting some pharmaceuticals and pesticides, but at concentration levels lower than the MRL.

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