Sub-minute method for simultaneous determination of aspartame, cyclamate, acesulfame-K and saccharin in food and pharmaceutical samples by capillary zone electrophoresis.

This paper reports the development of a sub-minute separation method by capillary zone electrophoresis for the determination of aspartame, cyclamate, acesulfame-K and saccharin in food products and pharmaceutical samples. Separations were performed in a fused uncoated silica capillary with UV detection at 220nm. Samples and standards were injected hydrodynamically using the short-end injection procedure. The electrophoretic system was operated under constant voltage of -30kV. The background electrolyte was composed of 45mmolL(-1) 2-amino-2-(hydroxymethyl)-1,3-propanediol and 15mmolL(-1) benzoic acid at pH 8.4. The separation time for all analytes was less than 1min. Evaluation of analytical parameters of the method showed good linearity (r(2)>0.9972), limit of detection of 3.3-6.4mgL(-1), intermediate precision better than 9.75% (peak area of sample) and recovery in the range of 91-117%.

New multilayer coating using quaternary ammonium chitosan and κ-carrageenan in capillary electrophoresis: application in fast analysis of betaine and methionine.

The aim of this study was to develop a new multilayer coating with crosslinked quaternary ammonium chitosan (hydroxypropyltrimethyl ammonium chloride chitosan; HACC) and κ-carrageenan for use in capillary electrophoresis. A new semi-permanent multilayer coating was formed using the procedure developed and the method does not require the presence of polymers in the background electrolyte (BGE). The new capillary multilayer coating showed a cathodic electroosmotic flow (EOF) of around 30×10(-9) m(2) V(-1) s(-1) which is pH-independent in the range of pH 2 to 10. The enhanced EOF at low pH obtained contributed significantly to the development of a fast method of separation. The multilayer coating was then applied in the development of a fast separation method to determine betaine and methionine in pharmaceutical formulations by capillary zone electrophoresis (CZE). The BGE used to determine the betaine and methionine concentrations was composed of 10 mmol L(-1) tris(hydroxymethyl) aminomethane, 40 mmol L(-1) phosphoric acid and 10% (v/v) ethanol, at pH 2.1. A fused-silica capillary of 32 cm (50 µm ID×375 µm OD) was used in the experiments and samples and standards were analyzed employing the short-end injection procedure (8.5 cm effective length). The instrumental analysis time of the optimized method was 1.53 min (approx. 39 runs per hour). The validation of the proposed method for the determination of betaine and methionine showed good linearity (R(2)>0.999), adequate limit of detection (LOD <8 mg L(-1)) for the concentration in the samples and inter-day precision values lower than 3.5% (peak area and time migration). The results for the quantification of the amino acids in the samples determined by the CZE-UV method developed were statistically equal to those obtained with the comparative LC-MS/MS method according to the paired t-test with a confidence level of 95%.

Simultaneous determination of free and total glycerol in biodiesel by capillary electrophoresis using multiple short-end injection.

A rapid method for the simultaneous determination of free glycerol (FG) and total glycerol (TG) in biodiesel by CE using a short-end multiple injection (SE/MI) configuration system is described. The sample preparation for FG involves the extraction of glycerol with water and for TG a saponification reaction is carried out followed by extraction as in the case of FG. The glycerol extracted in both cases is submitted to periodate oxidation and the iodate ions formed are measured on a CE-SE/MI system. The relevance of this study lies in the fact that no analytical procedure has been previously reported for the determination of TG (or of FG and TG simultaneously) by CE. The optimum conditions for the saponification/extraction process were 1.25% KOH and 25°C, with a time of only 5 min, and biodiesel mass in the range of 50.0-200.0 mg can be used. Multiple injections were performed hydrodynamically with negative pressure as follows: 50 mbar/3s (FG sample); 50 mbar/6s (electrolyte spacer); 50 mbar/3s (TG sample). The linear range obtained was 1.55-46.5 mg/L with R(2) > 0.99. The LOD and LOQ were 0.16 mg/L and 0.47 mg/L, respectively for TG. The method provides acceptable throughput for application in quality control and monitoring biodiesel synthesis process. In addition, it offers simple sample preparation (saponification process), it can be applied to a variety biodiesel samples (soybean, castor, and waste cooking oils) and it can be used for the determination of two key parameters related to the biodiesel quality with a fast separation (less than 30 s) using an optimized CE-SE/MI system.

Development of a fast and selective separation method to determine histamine in tuna fish samples using capillary zone electrophoresis.

This paper reports on the development of a fast and selective separation method by capillary zone electrophoresis (CZE) for the determination of histamine in tuna fish samples. The background electrolyte was composed of 60 mmol L(-1) hydroxyisobutyric acid and 10 mmol L(-1) sodium hydroxide at pH 3.3. The internal standard used was imidazole. Separations were performed in a fused uncoated silica capillary (32 cm total length, 8.5 cm effective length and 50 µm internal diameter) with direct UV detection at 210 nm. The samples and standards were injected hydrodynamically (50 mbar, 3s) from the outlet capillary end (nearest to the detector) and the electrophoretic system was operated under normal polarity and constant voltage conditions of 30 kV (positive polarity on the injection side). The migration time of histamine in the proposed method was only 0.34 min. The method was then validated and different tuna fish samples were analyzed. Good linearity (R(2)>0.999), a limit of detection 0.14 mg L(-1), intra-day precision better than 3.5% (peak area of sample), and recovery in the range of 94-108% were obtained. The results of the histamine concentration determined in the samples by the CZE method were compared with the LC-MS/MS method.

Simultaneous adsorption of iron and manganese from aqueous solutions employing an adsorbent coal.

In this work, an adsorbent coal was characterized and its sorption properties for the removal of iron and manganese from aqueous solutions were determined. Energy dispersive X-ray (EDX) analysis and X-ray diffraction (XRD) identified the presence of quartz, magnetite and manganese oxide in the adsorbent coal. The results of the adsorption isotherms verified the adsorption of iron and manganese by adsorbent coal showing a linear behaviour and indicated that chemisorption and physisorption occurred. The kinetic results were best adjusted to the pseudo-second order model with a 0.999 correlation coefficient. The results showed that the adsorbent coal could be used efficiently for the removal of iron and manganese from aqueous solutions.

Increasing the instrumental throughput of gas chromatography method using multiple injections in a single experimental run: application in determination of friedelan-3-ol and friedelin in Maytenus ilicifolia.

The aim of this study was to develop a separation method using multiple injections in a single experimental run (MISER) employing gas chromatography with flame ionization detection (GC-FID) for the first time, without instrument modification, to increase the instrumental throughput. The method was applied to the determination of the triterpenes friedelan-3-ol and friedelin in a plant extract obtained from Maytenus ilicifolia leaves. The column used in the chromatography system was a ZB-50 (30 m × 0.25 mm × 0.15 µm) with 50% phenyl-50% methyl-polysiloxane. The samples (1.0 µL) were injected using the split mode (1:90), with the injector at 280 °C and FID detector at 320 °C. The column temperature was programmed to isothermal mode at 300°C. Helium was used as the carrier gas with a constant flow of 1.5 mL min(-1). It was possible to perform three injections in the same run using the MISER method. An increase in the instrumental throughput by a factor of around 2.6 was observed when the use of multiple injections was compared with the single injection method. This method showed good linearity for both analytes with R(2)>0.99 and the values for the limit of detection were 0.24 mg L(-1) and 0.44 mg L(-1), for friedelan-3-ol and friedelin, respectively. Furthermore, the values for the limits of quantification were 0.79 mg L(-1) for friedelan-3-ol and 1.16 mg L(-1) for friedelin. The proposed method has potential for other GC applications, allowing an increase in the instrumental throughput of the methods by applying this separation technique.