2019
DOI: 10.1016/j.talanta.2019.03.062
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Simultaneous determination of non-steroidal anti-inflammatory drugs and natural estrogens in the mussels Mytilus edulis trossulus

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Cited by 35 publications
(25 citation statements)
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“…The extraction efficiencies of polar drugs: paracetamol (logP 0.46), terbutaline (logP 0.90), and nadolol (logP 0.81), decreased significantly where the ASE extracts obtained at 50 • C were subjected to acidification prior SPE ( Figure 2B). Similar results were observed in our previous study concerning the development of a method for determining NSAIDs and natural estrogens in the mussel Mytilus edulis trossulus [38]. In summary, based on the obtained results, the application of the mixture of MeOH:H 2 O (1:1, v/v) at 50 • C without the acidification of the ASE extract prior to SPE purification was chosen as the most optimal ASE-SPE conditions for the isolation of target compounds from plant material.…”
Section: Type Of Solvents/ Temperature/ Pharmaceuticalssupporting
confidence: 91%
“…The extraction efficiencies of polar drugs: paracetamol (logP 0.46), terbutaline (logP 0.90), and nadolol (logP 0.81), decreased significantly where the ASE extracts obtained at 50 • C were subjected to acidification prior SPE ( Figure 2B). Similar results were observed in our previous study concerning the development of a method for determining NSAIDs and natural estrogens in the mussel Mytilus edulis trossulus [38]. In summary, based on the obtained results, the application of the mixture of MeOH:H 2 O (1:1, v/v) at 50 • C without the acidification of the ASE extract prior to SPE purification was chosen as the most optimal ASE-SPE conditions for the isolation of target compounds from plant material.…”
Section: Type Of Solvents/ Temperature/ Pharmaceuticalssupporting
confidence: 91%
“…To further evaluate the feasibility of the proposed method, determination of target EDCs in milk samples was performed. The spiking recoveries of EDCs were determined by adding the mixture of standard EDCs with concentrations of 1, 10 and 100 μg/L, and calculated based on Equation 40 : normalR()%=CspikedCmatrixCstandard×100% where C spiked , C matrix and C standard represent the concentrations of spiked, unspiked samples and standard solution, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Recoveries and precisions were measured by the proposed method in meat samples with spiking standards at three concentrations (10, 100 and 200 μg kg −1 ). Recoveries ( R ) were determined on the basis of Eqn (4): 33,41 R()%=CspikedCmatrixCstandard×100% in which C spiked , C matrix and C standard represent concentrations of spiked, unspiked meat samples and standard solution, respectively.…”
Section: Resultsmentioning
confidence: 99%