a Daniel

Determination of biogenic amines in beer and wine by capillary electrophoresis-tandem mass spectrometry

A capillary electrophoresis-tandem mass spectrometry (CE-MS/MS) method for the simultaneous assessment of nine biogenic amines (spermine, spermidine, putrescine, cadaverine, histamine, phenylethylamine, tryptamine, tyramine, and urocanic acid) in commercial samples of beer and wine is introduced. The samples were submitted to a simple clean-up step with poly(vinylpolypyrrolidone) followed by filtration. Electrophoretic separation in a polyvinyl alcohol (PVA)-coated capillary using 0.5 mol L(-1) acetic acid (pH 2.5) as background electrolyte and detection by electrospray-tandem mass spectrometry was employed. The range of the correlation coefficients of the calibration curves of the analyzed compounds was 0.996-0.999, and the limits of detection and limits of quantification were in the range of 1-2 μg L(-1) and 3-8 μg L(-1), respectively. The recovery values for samples spiked at three concentration levels (0.2, 0.5, and 1.0 mg L(-1)) ranged from 87 to 113% with standard deviation not greater than 5.8%. The use of a PVA-coated silica capillary allows suppressing the electroosmotic flow and, consequently, increasing of the separation efficiency. The method was successfully used to determine biogenic amines in commercial samples of beer and wine.

Degradation of caffeine by photo-Fenton process: optimization of treatment conditions using experimental design.

The degradation of caffeine in different kind of effluents, via photo-Fenton process, was investigated in lab-scale and in a solar pilot plant. The treatment conditions (caffeine, Fe(2+) and H(2)O(2) concentrations) were defined by experimental design. The optimized conditions for each variable, obtained using the response factor (% mineralization), were: 52.0 mg L(-1)caffeine, 10.0 mg L(-1)Fe(2+) and 42.0 mg L(-1)H(2)O(2) (replaced in kinetic experiments). Under these conditions, in ultrapure water (UW), the caffeine concentration reached the quantitation limit (0.76 mg L(-1)) after 20 min, and 78% of mineralization was obtained respectively after 120 min of reaction. Using the same conditions, the matrix influence (surface water - SW and sewage treatment plant effluent - STP) on caffeine degradation was also evaluated. The total removal of caffeine in SW was reached at the same time in UW (after 20 min), while 40 min were necessary in STP. Although lower mineralization rates were verified for high organic load, under the same operational conditions, less H(2)O(2) was necessary to mineralize the dissolved organic carbon as the initial organic load increases. A high efficiency of the photo-Fenton process was also observed in caffeine degradation by solar photocatalysis using a CPC reactor, as well as intermediates of low toxicity, demonstrating that photo-Fenton process can be a viable alternative for caffeine removal in wastewater.

Optimization of fipronil degradation by heterogeneous photocatalysis: Identification of transformation products and toxicity assessment.

In this work it was studied the degradation of the insecticide fipronil (FIP) by heterogeneous photocatalysis induced by TiO2 P25. Using chemometric methods (Factorial Design and Response Surface Methodology), it was possible to evaluate the role of interaction between pH of the reaction medium, the reaction time and concentration of TiO2, optimizing the conditions for degradation using artificial radiation. Under the optimized conditions (79.4xa0mgxa0L-1 TiO2 and 66.3xa0min of reaction time for 1.1xa0mgxa0L-1 of FIP, at pH 5.6-5.8 (natural pH of the irradiated suspension)), 90.9% of FIP degradation was achieved at a degradation rate of 1.54xa0×xa010-2xa0m2xa0kJ-1 in terms of accumulated UVA radiation, corresponding to a pseudo-first order rate constant of 1.34xa0×xa010-2 min-1 and a half-life of 51.7xa0min. Under the same conditions, these assays were extended to the use of solar radiation, when the degradation rate was 14% higher, with half-life of 45xa0min, suggesting that in both cases FIP degradation was successful. Four by-products of FIP photocatalytic degradation could be separated, identified, and their formation and consumption followed by UHPLC-Q-TOF. Although the same intermediates have been obtained using both irradiation sources, a faster degradation of the transformation products (TPs) was observed under solar irradiation due to its expressive photonic flux covering the UVA and UVB. It is noteworthy that both the untreated effluent and the identified compounds have low toxicity with respect to V.xa0fischeri, suggesting that the heterogeneous photocatalysis may be a good alternative for treatment of wastewaters containing FIP and its TPs, mainly when solar radiation is the source of radiation, since under this condition the power consumption during the treatment can be significantly reduced.

Determination of halosulfuron-methyl herbicide in sugarcane juice and tomato by capillary electrophoresis–tandem mass spectrometry

A capillary electrophoresis-tandem mass spectrometry (CE-MS/MS) method for the determination of halosulfuron-methyl (HSU) residue in samples of sugarcane juice and tomato is introduced and validated. The samples were submitted to a QuEChERS extraction procedure followed by electrophoretic separation in NH4HCO3 electrolyte (adjusted to pH 8.5) and detection by electrospray-tandem mass spectrometry. The total HSU migration took place in less than 3.5 min, and the detection was accomplished by monitoring three fragmentation processes of this anion: m/z 435-182, 139, and 83. The R(2) values for concentrations up to 100 ppb (μg kg(-1)) were, respectively, 0.992, 0.992, and 0.978. Recovery values for samples spiked at three concentration levels (10, 20 and 50 ppb) were in the range of 96-104% with standard deviation not greater than 5.0%. The limit of detection for HSU in sugarcane juice and tomato was 2 ppb for both samples.

Photolytic degradation of chloramphenicol in different aqueous matrices using artificial and solar radiation: reaction kinetics and initial transformation products

The photodegradation of cloramphenicol (CAP) in ultrapure water (UW), untreated surface water (USW), and treated effluent from sewage treatment plant (TESTP) in laboratory scale and pilot scale, was evaluated using solar and artificial radiation. The results show, in all cases, that the CAP degradation occurs according to pseudo-first order kinetics, with the apparent degradation rate constants (kapp) following the order UW ≡ USW > TESTP. The kapp and half-life were strongly influenced by the radiation source. Mono- and di-hydroxyl transformation products were identified in UW after 40 min of solar irradiation, while the acute toxicity to Artemia salina increased from 35% to 100%, respectively after 180 and 1440 min of artificial and solar irradiation (94 and 132 kJ L-1), when 99.2 and 97.7% of CAP degradation occurred. The transformation products did not present antimicrobial activity.

Detection of coffee adulteration with soybean and corn by capillary electrophoresis-tandem mass spectrometry

The detection of coffee adulteration with soybean and corn by capillary electrophoresis-tandem mass spectrometry was accomplished by evaluating the monosaccharides profile obtained after acid hydrolysis of the samples. The acid hydrolysis, using H2SO4 as a catalyst, increases the ionic strength of the sample impairing the electrophoretic separation. Therefore, Ba(OH)2 was used to both neutralize the medium and reduce the content of sulfate by precipitation of BaSO4. The best separation of nine determined monosaccharides (fucose, galactose, arabinose, glucose, rhamnose, xylose, mannose, fructose and ribose) plus inositol as internal standard was obtained in 500u202fmmol·L-1 triethylamine, pH 12.3. The monosaccharides are separated as anionic species at this pH. The proposed method is simple, fast (<12.0u202fmin), present linear calibration curves (r2u202f=u202f0.995), and relative standard deviation for replicate injections lower than 5%. The LOQ for all monosaccharides was lower than 0.01u202fmmol·L-1, which is in accordance with the tolerable limits for coffee. Principal component analysis (PCA) was used to evaluate interrelationships between the monosaccharide profile and the coffee adulteration with different proportions of soybean and corn. Fucose, galactose, arabinose, glucose, sucrose, rhamnose, xylose, mannose, fructose, and ribose were quantified in packed roast-and-ground commercial coffee samples, and differences between adulterated and unadulterated coffees could be detected.

Amphetamine and derivatives in natural weight loss pills and dietary supplements by capillary electrophoresis-tandem mass spectrometry

A capillary electrophoresis-tandem mass spectrometry (CE-MS/MS) method for amphetamine (AM), phentermine (PTM), methamphetamine (MAM), methylenedioxyamphetamine (MDA), methylenedioxymethamphetamine (MDMA), and methylenedioxyethylamphetamine (MDEA) in commercial samples of homeopathic and phytotherapic medicines and dietary supplements is presented. The samples were submitted to a modified QuEChERS extraction procedure (at apparent pH 13) followed by electrophoretic separation in 0.1molL-1 formic acid electrolyte (pH 2.4) and detection by ESI-MS/MS. A polyvinyl alcohol coated capillary was employed to prevent the adsorption of the analytes to the capillary wall. The limits of detection and quantitation were from 0.02 to 0.06μgL-1 and from 0.06 to 0.21μgL-1, respectively, with recovery ranging from 85 to 123% and the standard deviations were not greater than 6.1%. In addition, the separation occurs in less than six minutes.

A capillary electrophoresis/tandem mass spectrometry approach for the determination of monoalkyl carbonates

The hemiesters of carbonic acid, which include the monoalkyl carbonates (MACs), are a poorly-known class of species with potential interest for biological processes. Capillary electrophoresis (CE) with tandem mass spectrometry is herein introduced as a complementary technique to CE with capacitively coupled contactless conductivity detection (C4D) for the study of MACs. Multiple reactions monitoring mode was used to improve sensitivity and selectivity, the loss of CO2 (44 u) at low collisional energy being the key feature of the MACs. To improve the control over the temperature – and consequently over the hydrolysis of the MACs during the electrophoretic migration – a thermostating case for the silica capillary was developed. Quantitation was possible by using the estimated concentration of MAC from the initial concentrations of the reagents and the equilibrium constant in the calibration procedure. The LOD for monoethyl carbonate was 0.2 μmol L−1, which is ca. two orders of magnitude lower than the LOD obtained by CE-C4D. Using a modified BGE for the separation of MACs, the LODs for mono-3-pentyl, mono-1-butyl, mono-2-propyl, and monoethyl carbonates were 0.2, 0.5, 2, and 1.3 μmol L−1, respectively.

Fast analysis of terbutaline in pharmaceuticals using multi-walled nanotubes modified electrodes from recordable compact disc.

In this study, homemade disposable gold electrodes made from recordable compact disks were modified with carbon nanotubes for amperometric quantification of terbutaline sulfate in pharmaceutical products. A flow cell using an impingent jet of solution on the electrode surface was build and used for amperometric detection, and a series of experiments were carried out to find the best experimental conditions for the new electrode in a specially designed cell. A linear response for terbutaline was obtained in the range from 3.0xa0×xa010(-6) to 5.0xa0×xa010(-4)xa0molxa0L(-1) (at 0.63xa0V vs. Ag/AgCl). The limits of detection and quantification were calculated as 5.8xa0×xa010(-7)xa0molxa0L(-1)xa0(S/Nxa0=xa03) and 1.9xa0×xa010(-6)xa0molxa0L(-1)xa0(S/Nxa0=xa010), respectively. A frequency of 30xa0injectionsxa0h(-1) was attained. The proposed method was successfully applied to the analyses of commercial syrup samples, and all results were in good agreement with those obtained by using high performance liquid chromatography and capillary electrophoresis-tandem mass spectrometry.

Moxidectin residues in lamb tissues: Development and validation of analytical method by UHPLC-MS/MS

The development and validation of a throughput method for the quantitation of moxidectin residues in lamb target tissues (muscle, kidney, liver and fat) was conducted using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). To achieve higher recovery of the analyte from the matrices, a modified QuEChERS method was used for sample preparation. The chromatographic separation was achieved using a Zorbax Eclipse Plus C18 RRHD column with a mobile phase comprising 5mM ammonium formate solutionu2009+0.1% formic acid (A) and acetonitrileu2009+0.1% formic acid (B) in a linear gradient program. Method validation was performed based on the Commission Decision 2002/657/EC and VICH GL49. To quantify the analyte, matrix-matched analytical curves were constructed with spiked blank tissues, with a limit of quantitation of 5ngg-1 and limit of detection of 1.5ngg-1 for all matrices. The linearity, decision limit, detection capability accuracy, and inter- and intra-day repeatability of the method are reported. The method was successfully applied to incurred lamb tissue samples (muscle, liver, kidney and fat) in a concentration range from 5 to 200μgkg-1, which demonstrated its suitability for monitoring moxidectin residues in lamb tissues in health surveillance programs, as well as for pharmacokinetics and residue depletion studies.