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PubMed2000

Normal and differential demasking flow-injection manifold for the direct spectrophotometric determination of zinc(II) in biological materials and pharmaceutical formulations.

A normal and a differential demasking flow-injection (FI) manifold were developed and optimized for the spectrophotometric determination of microamounts of Zn(II) in biological materials and pharmaceutical formulations. The reported method is very sensitive, rapid, simple and it is based upon the reaction of Zn(II) with 2,2'-dipyridyl-2-pyridylhydrazone (DPPH) in a strongly basic medium to form a yellow-coloured complex (lambda max = 448 nm). By using the differential demasking manifold, the tolerance of the method to many cations was enhanced by a mean factor of 25. The obtained calibration graphs were linear in the range of 0-10 mg l-1 Zn(II), at a sampling rate of 120 injections h-1 in both cases. The precisions of both manifolds were very good (RSD = 0.6 and 0.8%, respectively) and the 3 sigma detection limits were quite satisfactory (cL = 4 and 6 ng ml-1 respectively). The method has been successfully applied to the determination of Zn(II) in serum, human hair and pharmaceutical formulations with recoveries ranging between 98.0 and 101.6%. The obtained results were also in excellent agreement with flame atomic absorption spectrometry (FAAS), since the mean relative error was er = 0.9%.

Calibration↗
PubMed2001

Flow injection potentiometric determination of pipazethate hydrochloride.

New plastic membrane electrodes for pipazethate hydrochloride based on pipazethatium phosphotungstate, pipazethatium phosphomolybdate and a mixture of the two were prepared. The electrodes were fully characterized in terms of composition, life span, pH and temperature and were then applied to the potentiometric determination of the pipazethate ion in its pure state and pharmaceutical preparations under batch and flow injection conditions. The selectivity of the electrodes towards many inorganic cations, sugars and amino acids was also tested.

Benzothiadiazines↗
PubMed2001

Flow injection manifold for the direct spectrophotometric determination of bismuth in pharmaceutical products using Methylthymol Blue as a chromogenic reagent.

A new simple and rapid flow injection method is reported for the direct determination of bismuth in pharmaceutical products. Methylthymol Blue (MTB) was used as a chromogenic reagent and the absorbance of the colored Bi(III)-MTB complex produced was monitored at 548 nm. The various chemical and physical variables were optimized and a study of interfering ions was also carried out. Linear calibration graphs were obtained from 0 to 100 mg l-1 Bi(m) (120 injections per hour). The precision was very good (sr = 1.3%) and the limit of detection was cL = 0.150 mg l-1. The average accuracy was also very good (er = 0.75%) and was evaluated by comparison of the results obtained with those claimed by the manufacturers. The method was found to be adequately selective, considering the ions that the samples contain.

Bismuth↗
PubMed2001

Synchronous fluorescence and absorbance dynamic liquid drop sensor for cr(VI) determination at the femtomole level.

A novel synchronous fluorimetric and absorptiometric technique based on dynamic liquid drops coupled with flow injection is described for the determination of chromium(VI) in aqueous solutions. Drops formed continuously at the end of a quartz capillary tube serve as reactor and optical cell. The reaction between chromium(VI) and 3,3',5,5'-tetramethylbenzidine dichloride (TMB-d) results in a significant decrease in fluorescence and transmitted light intensity, proportional to the logarithm of the concentration of chromium(VI). The transmitted light and fluorescence emission are detected in counter and perpendicular positions of the excitation light by a photomultipler tube and photodiode, respectively. In HCl-NaOAc buffer solution (pH 3.29), the sensor has a wide linear calibration range of 2 x 10(-8)-1 x 10(-4) mol l(-1) chromium(VI) with an absolute mass detection limit of 12.88 fmol.

Calibration↗
PubMed2001

Blood platelet adhesion to protein studied by on-line acoustic wave sensor.

The attachment of blood platelets to the surface of bare and protein-coated thickness-shear mode acoustic wave devices operating in a flow-through configuration has been studied. Platelets in washed from bind to the gold electrodes of such sensors, but the resulting frequency shifts are far less than predicted by the conventional mass-based model of device operation. Adherence to albumin and various types of collagen can be produced by on-line introduction of protein or by a pre-coating strategy. Differences in attachment of platelets to collagen types I and IV and the Horm variety can be detected. Platelets attached to collagen yield an interesting delayed, but reversible signal on exposure to a flowing medium of low pH. Scanning electron microscopy of sensor surfaces at various time points in this experiment reveals that originally intact platelets are eventually destroyed by the high acidity of the medium. The reversible frequency is attributed to the presence of removable platelet granular components at the sensor-liquid interface.

Albumins↗
PubMed2001

Speciation and preconcentration of vanadium(V) and vanadium(IV) in water samples by flow injection-inductively coupled plasma optical emission spectrometry and ultrasonic nebulization.

An on-line separation, preconcentration and determination system for vanadium(IV) and vanadium(V) comprising inductively coupled plasma optical emission spectrometry (ICP-OES) coupled to a flow injection (FI) method with an ultrasonic nebulization (USN) system was studied. The vanadium species were retained on an Amberlite XAD-7 resin as a vanadium-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (V-5-Br-PADAP) complex at pH 3.7. Enhanced selectivity was obtained with the combined use of the formation on-line of the complexes and 1,2-cyclohexanediaminetetraacetic acid (CDTA) as masking agent. The vanadium complexes were removed from the microcolumn with 25% v/v nitric acid. A sensitivity enhancement factor of 225 was obtained with respect to ICP-OES using pneumatic nebulization (15-fold for USN and 15-fold for the microcolumn). The detection limit for the preconcentration of 10 mL of aqueous solution was 19 ng L-1. The precision for 10 replicate determinations at the 5 micrograms L-1 V level was 2.3% relative standard deviation (RSD), calculated from the peak heights obtained. The calibration graph using the separation and preconcentration system for vanadium species was linear with a correlation coefficient of 0.9992 at levels from near the detection limits up to at least 100 micrograms L-1. The method was successfully applied to the speciation of vanadium in river water samples.

Flow Injection Analysis↗
PubMed2001

A quartz crystal resonant sensor (QCRS) study of HSA--drug interactions.

Human serum albumin (HSA) was immobilised on the gold surface of a quartz crystal resonance sensor (QCRS) and exposed to warfarin and diazepam. Distinct decreases in frequency of differing magnitudes were observed upon exposure of the protein to each of the compounds suggesting strongly that a ligand interaction was occurring. Moreover, as sequential exposure in any order was observed to yield distinct repeatable frequency decreases for the ligands indicated, screening for site specific binding may be possible. Identically immobilised bovine serum albumin (BSA) gave no response to either compound.

Animals↗
PubMed2001

Determination of nitrite by inhibition of the chemiluminescence of acriflavine in a flow-injection assembly.

The indirect determination of nitrite was performed with a flow-injection assembly on the basis of the inhibition of the analytical output obtained in a luminometer by oxidation of acriflavine. The acriflavine solution merged with the nitrite and the resulting mixture was injected into a pure water stream. This solution merged with the oxidant solution (potassium permanganate in sulfuric acid medium) and the resulting chemiluminiscence was affected (inhibited) by the presence of nitrite after reaction with the aminoacridine. The method was applicable over the range 10-800 microg l(-1) of nitrite with a correlation coefficient of 0.9960. The relative standard deviation was 1.4% and the throughput was 76 samples h(-1). The influence of foreign substances was also tested. A solid-phase reactor, filled with Amberlite IRA-900, was inserted in the assembly for the on-line preconcentration of nitrite; the analytical output resulted in an increase of up to 11.5-fold. The method was applied to the determination of nitrites in residual waters, industrial formulations and soil samples.

Acriflavine↗
PubMed2001

Monoparameter sensors for the determination of the antioxidants butylated hydroxyanisole and n-propyl gallate in foods and cosmetics by flow injection spectrophotometry.

A flow-through optosensor with solid phase UV spectroscopic detection is proposed for the direct determination of single antioxidants, namely butylated hydroxyanisole (BHA) and n-propyl gallate (n-PG), without previous derivatization. The methods are based on the transient retention behaviour of these compounds in a flow-through cell packed with C-18 silica using ethanol-water mixtures as a carrier, and on the intrinsic absorbance monitored at 290 and 283 nm, respectively. After recording the analytical signal, the antioxidants were easily and quickly desorbed from the solid support by the same carrier. For BHA, calibration graphs were linear over the range 1.0-300.0 mg L-1 using area as the analytical parameter. The relative standard deviation (RSD) was between 0.5 and 1.6%. For n-PG, calibration graphs were linear over the range 1.0-300.0 mg L-1 in area and the RSD was between 1.4 and 1.5%. The methods were applied to the determination of these antioxidants in several food and cosmetics samples, and were validated using the standard additions method and an HPLC reference method.

Antioxidants↗
PubMed2001

Error-compensated kinetic determinations by detecting the reagent in successive reactions.

An error-compensated algorithm based on detecting the reagent in successive reactions is proposed. The algorithm was first studied by using simulated data and it was found that it performed well in compensating for the system error and eliminating random noise. Then the algorithm was examined by applying it to the determination of epinephrine and norepinephrine under different experimental conditions. The results revealed that the algorithm compensated errors produced not only by the changes of rate constants, but also by the variation of equilibrium signals.

Algorithms↗
PubMed2001

Two-parameter determination in vinegar by a flow injection-pervaporation system.

A flow injection method (FI) for the sequential determination of ethanol and acetic acid in vinegar is reported. The determination of ethanol is based on the oxidation of the pervaporated ethanol by K2Cr2O7. The acetic acid is determined by an acid-base reaction with Thymol Blue as the indicator. Both reactions are monitored photometrically at 600 nm using a single detector. Optimisation studies and assessment of the sequential Fl method are also reported. The linear determination range is 0-12% v/v for ethanol and 0-10% (grams of acetic acid in 100 ml) for acetic acid. The sample throughput of the sequential manifold is seven per hour. The new method was applied to vinegar samples and the results obtained were in excellent agreement with those from reference methods used in Spain.

Acetic Acid↗
PubMed2001

Fluorimetric determination of total ascorbic acid by a stopped-flow mixing technique.

A simple, rapid and automatic fluorimetric method for the determination of total ascorbic acid is described. The method makes use of the stopped-flow mixing technique in order to achieve the rapid oxidation of ascorbic acid by dissolved oxygen to dehydroascorbic acid, which then reacts with o-phenylenediamine to form a fluorescent quinoxaline. The initial rate and fluorescence signal of this system are directly proportional to the ascorbic acid concentration. The calibration graph was linear over the range 0.1-30 microg ml(-1) (kinetic method) and 0.25-34 microg ml(-1) (equilibrium method). The precision (% RSD) was close to 0.5%. The method has been used for the determination of ascorbic acid in pharmaceutical formulations, fruit juices, soft drinks and blood serum.

Ascorbic Acid↗
PubMed2001

Micro sequential injection: environmental monitoring of nitrogen and phosphate in water using a "Lab-on-Valve" system furnished with a microcolumn.

A "Lab-on-Valve" manifold operated in the micro sequential injection (microSI) mode was adopted to accommodate EPA-approved methods for spectrophotometric determinations of nitrate, nitrite and orthophosphate in the ppb (N or P) concentration range. A computer programmable microSI protocol, utilizing stopped-flow within a copperized Cd-foil filled microcolumn was developed for nitrate reduction to nitrite with subsequent colorimetric measurement, yielding concentration ranges for nitrate of 100.0-4000.0 ppb (N) and for nitrite of 30.0-4000.0 ppb (N) and linear calibration responses of r2 = 0.9999 for nitrate and 0.9995 for nitrite. Using a stopped-flow reaction rate measurement, phosphate was determined in the range 1.0-30.0 ppb (P) with a calibration response of r2 = 0.9997. The technical improvement of this methodology, apart from micro miniaturization, is the use of the stopped-flow technique, that resulted in improved detection limits and allowed reagent consumption to be reduced 1500-fold compared with conventional procedure while the amount of metallic cadmium was reduced 20-fold compared with the EPA-approved continuous-flow assay.

Flow Injection Analysis↗
PubMed2002

Mechanism of response enhancement in evaporative light scattering detection with the addition of triethylamine and formic acid.

Triethylamine with an equimolar amount of formic acid added to the mobile phase provides an enhancement of the evaporative light scattering detector (ELSD) response. After characterization of the influence of various parameters on the ELSD response, a sequential strategy was defined to elucidate this response enhancement. The response enhancement was more marked at low mobile phase flow rate, and was highly dependent on solutes and solvents. The influence of drift tube temperature on response enhancement with various solutes demonstrated that triethylamine and formic acid mainly act as mass amplifiers by the inclusion of triethylamine-formic acid clusters inside the droplets.

Chromatography, Liquid↗
PubMed2002

Amperometric detection of sulfur-containing compounds in alkaline media.

A copper-based chemically modified glassy carbon electrode (GC-Cu) was developed to be used as an amperometric sensor for electrochemically detecting several sulfur-containing compounds in alkaline media. Under optimised flow injection conditions the calibration curves for sulfite, sulfide, thiosulfate, cysteine, cystine, etc., were linear over three orders of magnitude of concentration. Detection limits were of the order of 0.04-1.5 microM. A simple and rapid method for determining sulfite in red and white wines by anion-exchange chromatography with electrochemical detection is described.

Chromatography, Ion Exchange↗
PubMed2002

Inductively coupled plasma mass spectrometric determination of heavy metals in sea-water samples after pre-treatment with a chelating resin disk by an on-line flow injection method.

A new on-line flow injection (FI) pre-treatment system using a disk-type chelating resin (5 mm diameter, 0.5 mm thickness) was developed for the simultaneous multi-element determination of trace metals in sea-water samples by inductively coupled plasma mass spectrometry (ICP-MS). A chelating resin possessing an iminodiacetate (IDA) functional group was used for the collection of trace elements and the elimination of alkali and alkaline earth metals in highly concentrated salt solution. A 1 ml volume of a sea-water sample (pH 5.5) was applied to the chelating resin disk. Considering the removal efficiency for Ca, 50 mM ammonium acetate buffer solution (pH 5.5) was chosen as a sample carrier. The enriched trace metals were eluted with 0.1 M nitric acid and the eluate flowed into the ICP-MS system. The processing time for one sample was < 6 min (350 s). One of the important observations is the possibility of working with a low recovery, even lower than 50%. For example, several elements such as Mn, Cr, As, Mo, Ba and U, the recovery of which was < 50% in a batch-wise method, showed good linearity and reproducibility. The proposed method was evaluated by analyzing two kinds of sea-water certified reference materials, CASS-4 and NASS-5. Analytical data for eight heavy metals, V, Mn, Co, Ni, Cu, Mo, Cd and U, obtained from the present study agreed well with the certified values.

Flow Injection Analysis↗
PubMed2002

Microsequential injection: anion separations using 'lab-on-valve' coupled with capillary electrophoresis.

Microsequential injection (microSI) has been successfully coupled with capillary electrophoresis (CE). Presented is the microSI-CE system, interfaced with an integrated Lab-on-Valve (LOV) manifold that provides an efficient sample delivery conduit and a versatile means of sample pretreatment along with total automation of the separation process. Programmable microSI protocols control all critical system peripherals to perform various types of CE sample injections automatically such as electrokinetic (EK) injection, hydrodynamic (HD) injection, and head column field amplification (HCFA) sample stacking injection. Novel features of the microSI-CE technique are demonstrated on assays of samples containing 10 anions that had been used previously as a model system. Calibration studies by EK sample injection yielded linear concentration ranges of 0.5-3.0 mM with linear regression responses of r2 = 0.9999 for both chloride and sulfate using conductivity corrected peak area (CCPA) as concentration responses. Calibration using an internal standard was studied at the same concentration range giving r2 = 0.9992 for both chloride and sulfate and r2 = 0.9997 for both when CCPA correction was deployed. With HCFA sample stacking injection, a linear concentration dynamic range of 0.034-3.419 mM for chloride and 0.014-1.408 mM for sulfate were produced with linear regression responses of r2 = 0.9999 for chloride and r2 = 0.9998 for sulfate.

Anions↗
PubMed2002

Continuous ultrasound-assisted extraction of hexavalent chromium from soil with or without on-line preconcentration prior to photometric monitoring.

A continuous ultrasound-assisted extractor was coupled to a photometric detector in order to obtain a fully automated approach for the determination of CrVI in soil. The use of a flow injection (FI) manifold as interface between the extractor and the photometric detector allowed the monitoring of CrVI after extraction in a continuous manner. The coloured complex formed between 1,5-diphenylcarbazide (DPC) and CrVI was used as recommended in EPA method 7196A because it is one of the most sensitive and selective reactions for CrVI determination. A preconcentration minicolumn packed with a strong anion-exchange resin was placed between the extractor and the detector, providing a more sensitive method. The linear dynamic ranges were 1-10 and 0.25-7.5 mg l-1 for the methods without (method A) and with preconcentration (method B), respectively. The limits of detection were 4.52 ng for method A and 1.23 ng for method B. Both methods were applied to a natural contaminated soil and the results obtained agreed well with those obtained by the reference EPA method 3060A. The influence of different amounts of CrIII in the samples was also studied and the results showed that the proposed methods did not disturb the original species distribution.

Chromium↗