Dragana Mutavdžić Pavlović

Development and optimization of the SPE procedure for determination of pharmaceuticals in water samples by HPLC-diode array detection.

This paper focuses on the investigation of different types of SPE sorbents for the preconcentration of eight veterinary pharmaceuticals from water samples. The pharmaceuticals studied were sulfamethazine, sulfadiazine, sulfaguanidine, trimethoprim, oxytetracycline, enrofloxacin, norfloxacin and penicillin G/procaine. Five different SPE materials (Strata-X, Strata-X-C, Strata SDB-L, Strata C8 and Strata C18) from Phenomenex were compared with Oasis HLB with a view to obtaining the best cartridges for all pharmaceuticals investigated. Extraction efficiency was determined by HPLC with diode array detection (DAD). HPLC-DAD separation and quantification of the selected pharmaceuticals were carried out under gradient elution by a binary mixture of 0.01 M oxalic acid and ACN based on cyano modified column (LiChrosphere 100 CN) from Merck. Strata-X provided the best results in the preconcentration of 100 mL water samples, yielding average pharmaceutical recoveries of higher than 90%, except for sulfaguanidine (76.1%). The developed Strata-X-HLPC-DAD method was validated and applied, for the efficient investigation of reverse osmosis/nanofiltration membranes and for the removal of these eight pharmaceuticals from the production wastewater samples. NF90 and XLE membranes were shown to be the best for the rejection of all investigated pharmaceuticals.

Optimization of matrix solid-phase dispersion for liquid chromatography tandem mass spectrometry analysis of 12 pharmaceuticals in sediments.

The matrix solid-phase dispersion (MSPD) technique accompanied with LC-MS/MS detection for the purpose of determination of 12 pharmaceuticals (sulfaguanidine, sulfadiazine, sulfamethazine, sulfamethoxazole, trimethoprim, roxithromycin, praziquantel, febantel, enrofloxacin, ciprofloxacin, norfloxacin and procaine) applied to sediment samples has been described in this paper. Different parameters, such as the type of solid phase, the elution solvent and its volume have been investigated. The analytes were successfully extracted by C18 as an MSPD sorbent with 5 mL of acetonitrile:5% of oxalic acid=6:4 (v/v) as an elution solvent. The proposed method provides a linear response over the concentration range of 0.0005-100 μg/g, depending on pharmaceuticals with correlation coefficients above 0.9928 in all cases except for trimethoprim (0.9889). Also, the method has revealed low limits of detection (0.125-500 ng/g), good precision (intra and inter-day), a relative standard deviation below 15% and recoveries above 80%, except for roxithromycin, febantel and enrofloxacin. The method has been successfully applied to analysis of different sediment samples.

The sorption of sulfamethazine on soil samples: Isotherms and error analysis

In this paper, batch sorption of sulfamethazine on eight soil samples (six from Croatia and two from Bosnia and Hercegovina) with different organic matter contents ranging from 1.52 to 12.8% was investigated. The effects of various parameters such as agitation time, initial concentration, and ionic strength on the sulfamethazine sorption were studied. The experimental data were analysed using a one-parameter model, Linear isotherm, and two two-parameter models, the Freundlich and Dubinin-Radushkevich isotherms. The goodness of fit was measured using the linear regression and the determination coefficient (R(2)) value. Also, the equilibrium data of the two-parameter models were analysed using the residual root mean square error (RMSE), the sum of squares of errors (ERRSQ), and a composite fractional error function (HYBRID). Non-linear regression has better characteristics for analysing experimental data. The obtained sorption coefficients Kd (from 0.25 to 8.10 mL/g) and the Freundlich sorption coefficients KF (from 1.16 to 7.99 (μg/g)(mL/μg)(1/n)) exhibited quite low values, which indicated that sulfamethazine is weakly adsorbed on the evaluated soils, is highly mobile, and has a great potential to penetrate and pollute the ground water. The Dubinin-Radushkevich isotherm was used to estimate the apparent free energy of sorption.

RO/NF membrane treatment of veterinary pharmaceutical wastewater: comparison of results obtained on a laboratory and a pilot scale

BackgroundEmerging contaminants (ECs) are commonly derived from industrial wastewater, which is often a consequence of an inadequate treatment of the latter. Improperly pretreated pharmaceutical wastewater could cause difficulties in operations of wastewater treatment plants while incomplete elimination of ECs during the processing might result in their appearance in drinking water.MethodsThis paper deals with membrane treatment of pharmaceutical wastewater on a laboratory and a pilot scale as well as with the removal of the following veterinary pharmaceuticals (VPs) (sulfamethoxazole, trimethoprim, ciprofloxacin, dexamethasone, and febantel).ResultsThe pretreatment of pharmaceutical wastewater by means of coagulation and microfiltration (MF) prevented the irreversible fouling of the fine porous structure of the reverse osmosis (RO) and nanofiltration (NF) membranes which were used in the final stage of wastewater processing. The percentage of the removal of the selected VPs ranges from 94% to almost 100% in the case of NF and RO membranes in both scales. The recovery percentage concerning the pilot scale amounted to 88%. Membrane cleaning was successfully carried out in both scales.ConclusionsThe differences in retention between laboratory and pilot tests are due to different raw wastewater quality and different recovery and hydrodynamic of the two systems. Fouling and concentration polarization were more pronounced in laboratory setup (frame-plate module) than in pilot unit (spiral module). The proposed integrated membrane treatment (coagulation, MF, NF, and RO) can be employed for treatment of wastewater originating from pharmaceutical factory. The obtained permeate can be safely discharged to sewer system or could be reused in manufacturing process.

Novel multiresidue method for determination of pesticides in red wine using gas chromatography–mass spectrometry and solid phase extraction

A new multiresidue method was developed for determination of 25 pesticide residues in red wine by gas chromatography coupled to mass spectrometry with a single run of 23.63 min. Samples were extracted from wine with solid phase extraction using Oasis HLB. Mixture of methanol and water was used for rinsing, while acetonitrile and n-hexane were used as elution solvents. Method was validated according to SANCO/12571/2013 criteria in wide linearity range (limit of quantification - 400 μg L(-1)). Limits of quantification (LOQ) were well below 10 μg L(-1) for most pesticides and recoveries at 2×LOQ and 10×LOQ concentration levels were in range 70-120%. Precision, expressed as a relative standard deviation, was always under 14%. The method was applied to 32 red wine samples from Croatia. Pesticides were detected in 30 samples with a total of 15 pesticides found, 7 of which were at a high concentration.

SPE-HPLC/DAD determination of trimethoprim, oxytetracycline and enrofloxacin in water samples

In this paper high-performance liquid chromatography with diode array UV detection (HPLC/DAD) after SPE sample pretreatment for simultaneous analysis of pharmaceuticals from three different classes: enrofloxacin, oxytetracycline and trimethoprim, has been developed, optimised and validated. The chromatographic separation was developed on spiked wellspring water samples and checked on model wastewater samples of veterinary pharmaceuticals before and after RO/NF membrane treatment (feed and permeate streams) and on process wastewaters of industrial origin. Chromatographic separation was performed on Varian ProStar HPLC/DAD with C-18 column (Microsorb-MV 100 C18, 150 × 4.6 mm; 5 µm, Varian, USA). Detection and quantification was performed at 254 nm. The best separation was achieved with mobile phase 0.5% formic acid and 1% trifluoroacetic acid in 0.05 M ammonium acetate-methanol, 70 + 30, (v/v) after extraction procedure on polystyrenedivinylbenzene Varian Empore extraction disks. The extraction efficiency was checked by recovery experiments.

Development and optimization of the determination of pharmaceuticals in water samples by SPE and HPLC with diode-array detection

This paper describes the development, optimization, and validation of a method for the determination of five pharmaceuticals from different therapeutic classes (antibiotics, anthelmintics, glucocorticoides) in water samples. Water samples were prepared using SPE and extracts were analyzed by HPLC with diode-array detection. The efficiency of 11 different SPE cartridges to extract the investigated compounds from water was tested in preliminary experiments. Then, the pH of the water sample, elution solvent, and sorbent mass were optimized. Except for optimization of the SPE procedure, selection of the optimal HPLC column with different stationary phases from different manufacturers has been performed. The developed method was validated using spring water samples spiked with appropriate concentrations of pharmaceuticals. Good linearity was obtained in the range of 2.4-200 μg/L, depending on the pharmaceutical with the correlation coefficients >0.9930 in all cases, except for ciprofloxacin (0.9866). Also, the method has revealed that low LODs (0.7-3.9 μg/L), good precision (intra- and interday) with RSD below 17% and recoveries above 98% for all pharmaceuticals. The method has been successfully applied to the analysis of production wastewater samples from the pharmaceutical industry.

Determination of thermodynamic pKa values of pharmaceuticals from five different groups using capillary electrophoresis

A determination of the thermodynamic acid dissociation constants (pKa) of 22 frequently used pharmaceuticals using capillary electrophoresis in aqueous media is presented in this work. The investigated pharmaceuticals belong to different pharmacological groups: macrolides, fluoroquinolones, sulfonamides, β-lactams, tetracyclines, and other miscellaneous pharmaceuticals. The electrophoretic mobilities of the investigated analytes were monitored in a pH range from 2.00 to 10.82. The data were fitted with an appropriate mathematical model using a nonlinear regression analysis to obtain pKa values. Experimentally obtained data were well described by the mathematical model chosen for each analyte that was confirmed by r(2) values higher than 0.99 for most of the investigated analytes. Extrapolations to zero ionic strength were used to determine the thermodynamic pKa values. Experimentally obtained acid dissociation constants were interpreted using structural formulae of investigated analytes and the moieties corresponding to specific pKa were identified.

Development and validation of a SPE-GC-MS method for the determination of pesticides in surface water

A method for analysis of 20 commonly used pesticides in surface water based on solid-phase extraction and gas chromatography-mass spectrometry was proposed. During method development the key parameters that can affect SPE extraction and determination such as selection of efficient SPE sorbent, pH of water sample, type and volume of elution solvent, breakthrough volume and matrix effects were investigated. The method was validated using spring water spiked with appropriate concentration of pesticides. The obtained correlation coefficients were in range 0.9972–1.000, limits of detection (LOD) were 0.001–0.5 µg L−1 and the limits of quantification (LOQ) were 0.005–1 µg L−1 depending on a pesticide. Much higher LOD (20 µg L−1) and LOQ (50 µg L−1) values were obtained for bentazone. The influence of matrix was assessed using real water samples spiked with appropriate concentration of pesticide standards solution. Both signal enhancement and suppression were observed, depending on a pesticide, therefore standard addition method was used for pesticides determination. The developed method was applied on real water samples taken in close vicinity of agricultural fields. Many of the targeted pesticides were found in the samples and the results are presented in this article.

Chapter 5 - Analysis of PhACs in Solid Environmental Samples (Soil, Sediment, and Sludge)

Abstract This chapter discusses about developed analytic methods and new approaches to pharmaceutically active compound (PhAC) determination in solid environmental samples including soil, sediment, and sludge. Solid environmental matrices represent a more challenging analytic task compared to water samples due to their high heterogeneity. Conventional and novel sample preparation methods are described and compared from the viewpoint of their applicability to environmental analysis. Since extraction methods are not selective, an additional cleanup step usually follows the sample preparation procedure. With respect to separation and detection of PhACs in extracts from solid environmental samples, advanced analytic methods are used. They are based on chromatographic techniques (gas chromatography or liquid chromatography (LC)) hyphenated to mass spectrometry (MS). Advance LC–MS methods applied in analysis of soil environmental samples are presen ted too.