Flow-injection chemiluminometric analysis of some benzamides by their sensitizing effect on the cerium-sulphite reaction

A simple, highly sensitive chemiluminescent method using flow injection is described for the determination of three substituted benzamides, namely: sulpiride, sultopride and tiapride. The method is based on the sensitizing effect of these drugs on the chemiluminometric oxidation of sulphite by cerium(IV). The different experimental parameters affecting the chemiluminescence intensity were carefully studied and incorporated into the procedure. The method permits the determination of 0.05-2.5 mug ml(-1) sulpiride, 0.01-2.5 mug ml(-1) sultopride hydrochloride and 0.01-1.5 mug ml(-1) tiapride hydrochloride with minimum detectability of 0.01 mug ml(-1). The method was applied to the determination of these benzamides in pharmaceutical preparations and biological fluids.     

Flow injection chemiluminescence determination of thiamine based on its enhancing effect on the luminol-hydrogen peroxide system

A new flow injection chemiluminescence (CL) method is proposed for the determination of thiamine, based upon its enhancing effect on the CL reaction of luminol with hydrogen peroxide in alkaline solution. The method allows the determination of thiamine within 0.05-8 mug ml(-1) range with a detection limit (3sigma) of 0.01 mug ml(-1). The relative standard deviation is 1.4% (n=11, 0.5 mug ml(-1) thiamine) and the sample throughput is about 90 samples h(-1). The method was successfully applied to the determination of thiamine in pharmaceutical preparations.     

Simultaneous determination of manganese and zinc in mixtures using first- and second-derivative spectrophotometry

A new direct spectrophotometric determination of manganese with 5,8-dihydroxy-1,4-naphthoquinone (naphthazarin,NAZA) is reported. Absorption maximum, molar absorptivity and Sandell's sensitivity of 1:2 (M:L) complex are 695 nm, 1.88x10(4) l mol(-1) cm(-1) and 2.92 ng cm(-2), respectively. A linear calibration graph is obtained up to a concentration of 7.2 mug ml(-1) of manganese. The optimum range for determination (Ringbom) is between 0.20 and 6.8 mug ml(-1). A rapid method for simultaneous determination of manganese and zinc in their mixture using derivative spectra is described. The range 0.28-5.6 mug ml(-1) manganese could be determined in the presence of 0.33-6.8 mug ml(-1) zinc and vice versa. The developed method was applied to the simultaneous spectrophotometric determination of manganese and zinc in some synthetic mixtures and was found to give satisfactory results.     

Spectrophotometric multicomponent determination of sunset yellow, tartrazine and allura red in soft drink powder by double divisor-ratio spectra derivative, inverse least-squares and principal component regression methods

Double divisor-ratio spectra derivative (graphical method), classical least-squares and principal component regression (two numerical methods) methods were developed for the spectrophotometric multicomponent analysis of soft drink powders and synthetic mixtures containing three colorants without any chemical separation. The graphical method is based on the use of derivative signals of the ratio spectra using double divisor. In this method, the linear determination ranges were 2-8 mug ml(-1) sunset yellow, 4-18 mug ml(-1) tartrazine and 2-8 mug ml(-1) allura red in 0.1 M HCl. In the numerical methods, a training set was randomly prepared by using 18 samples containing between 0 and 8 mug ml(-1) of sunset yellow, 0-18 mug ml(-1) of tartrazine and 0-8 mug ml(-1) of allura red. The chemometric calibrations were calculated by using the prepared training set and its absorbances at seven points (from 375.0 to 550.0 nm) in the spectral region 325-584 nm. The proposed methods were validated by using synthetic ternary mixtures and applied to the simultaneous determination of three colorants in soft drink powders. The obtained results were statistically compared with each other.     

Determination of trace europium based on new fluorimetric system of europium(III) with thenoyltrifluoroacetone and N,N'-dinaphthyl-N,N'-diphenyl-3,6-dioxaoctanediamide

In the present paper, N,N'-dinaphthyl-N,N'-diphenyl-3,6-dioxaoctanediamide acts as a specific reagent for enhancing the fluorescence intensity of Eu(III) complex with thenoyl trifluoroacetone (TTA), the spectrofluorimetric determination of trace amounts of Eu(III) based on the above system was carried out and its luminescence mechanism was studied. The excitation and emission wavelengths are 343.6 and 613.3 nm, respectively. The fluorescence intensities vary linearly with the concentration of europium(III) in the range 3.647x10(-3)-3.039 mug ml(-1) for the original fluorescence with a detection limit down to 2.279x10(-4) mug ml(-1) and the standard deviation is 0.063 mug ml(-1) for 10 times measurements, and in the range 7.598x10(-4)-0.0243 mug ml(-1) (SD=0.035 for 15 times measurements), 0.06078-0.6100 mug ml(-1) (SD=0.52 for 10 times measurements) for the first derivative fluorescence signal with a detection limit down to 8.566x10(-5) mug ml(-1). The interferences of other rare earths and some of inorganic ions are described. This method is a direct, rapid, selective and sensitive analytical method for the determination of trivalent europium in rare earth ore samples and high purity of rare earth oxides.     

Simultaneous determination of iron and zinc by pH gradient construction in a flow-injection system

A flow-injection method for the simultaneous determination of iron and zinc in the human hair with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP) using a pH gradient technique has been developed. The linear range for the determination of iron is 0.1 approximately 1.8 mug ml(-1) and for zinc is 0.2 approximately 5.0 mug ml(-1). About 20 approximately 30 samples can be determined in 1 h. The proposed method is simple, rapid and accurate. It has been applied to the simultaneous determination of trace amounts of iron and zinc in the human hair with satisfactory results.     

Determination of total proteins: a study of reaction between quinones and proteins

A previous study was undertaken to test the reaction of several quinones (p-benzoquinone; 2,5-dichloro and 2,6-dichloro p-benzoquinone; tetrachloro-p-benzoquinone; tetrachloro-o-benzoquinone; 2,5-dichloro-3,6-dihydroxy-p-benzoquinone; benz[a]anthracene-7,12-dione) with bovine serum albumin (BSA). From this study, we have devised a spectrophotometric method for determination of total proteins. The quinone, tetrachloro-p-benzoquinone (p-chloranil), showed the best result. The product of reaction between proteins and p-chloranil absorbed at 360 nm and Beer's law was followed up to 200 mug ml(-1) of BSA. The product of reaction of BSA/p-chloranil was stable for 30 min, after that the absorbance increased 16% and kept stable for 24 h. The p-chloranil method showed a limit of detection (1.25 mug ml(-1)) lower than the biuret method (52.0 mug ml(-1)) or p-benzoquinone (PBQ) method (2.6-4.0 mug ml(-1)). The method was applied to spectrophotometric determination of total proteins in blood plasma; the results were compared with the biuret method that is widely used in clinical analysis.     

Fluorimetric trace determination of cerium(III) with sodium triphosphate

Sodium triphosphate acts as a specific reagent for enhancing the fluorescence intensity of cerium(III). The purpose of this study was to investigate the spectrofluorimetric determination of trace amounts of Ce(III) in sodium triphosphate solution. The excitation and emission wavelengths are 303.5 nm and 353 nm respectively. Optimum sodium triphosphate concentration is found to be 0.074 g l(-1) at room temperature. The fluorescence varies linearly with the concentration of cerium(III) in the range 0.001-45 mug ml(-1). The detection limit is 9.4 x 10(-4)mug ml(-1). The relative standard deviations for 30 mug ml(-1) and 0.05 mug ml(-1) Ce(III) in 0.074 g l(-1) sodium triphosphate solution are 1.1% and 0.72% respectively. Quenching effects of other lanthanides and some inorganic anions are described. This method is a direct and rapid analytical method for the determination of Ce(III) in rare earth mixtures and cerium concentrates.     

Simultaneous determination of Ru(III) and Rh(III) using octadecyldithiocarbamate by first-derivative spectrophotometry

A first-derivative spectrophotometric method is described for the simultaneous determination of Ru(III) and Rh(III) using octadecyl dithiocarbamate. The complexes are insoluble in water, but easily extractable into chloroform. Quantitative determination of Ru(III) and Rh(III) is possible in the ranges 0.5-6.0 mug ml(-1) and 1.0-10.0 mug ml(-1) respectively, with a standard deviation of +/-0.10. A statistical evaluation of the experimental results is reported.     

Determination of clenbuterol in pharmaceutical preparations by reaction with o-phthalaldehyde using a flow-injection fluorimetric procedure

A new procedure for the determination of clenbuterol is proposed using flow-injection and fluorimetric detection. The method is based on the derivatization reaction of the primary amine group with o-phthalaldehyde in the presence of 2-mercaptoethanol. The calibration graph based on peak area was linear in the range 0.2-5 mug ml(-1) and the detection limit was 0.06 mug ml(-1). The method was validated using a reference spectrophotometric procedure and was applied to the determination of the drug in commercial pharmaceutical preparations.     

Application of a microbial sensor to the quality control of meat freshness

Isosorbide dinitrate (ISDN) is reduced voltammetrically at gold working electrode surface in aqueous sodium sulfite solution and produces a voltammogram with its peak current proportional to the concentration of ISDN in the range of 1.3-2340 mug ml(-1). Sodium sulfite is used as supporting electrolyte and oxygen removing agent and, therefore, no nitrogen gas purging for elimination of soluble oxygen in, the sample solution is required. The limit of detection (LOD) of the method is 0.0838 mug ml(-1) and the relative standard deviation (R.S.D.) of 24 replicate determination of 52 mug ml(-1) of ISDN is 3.60%. The method is used for quantitative analysis of ISDN in arterial plasma, synthetic serum and pharmaceutical dosage form. The results are compared with those obtained from GC determination method. The method is sensitive and requires little sample preparation in a wide concentration range.     

Studies on 1:12 phosphomolybdic heteropoly anion film modified carbon paste electrode

A 1:12 phosphomolybdic anion film modified carbon paste electrode (PMo(12) electrode) is prepared by electrochemical deposition and its application is studied by cyclic voltammetry. The film modified electrode can adsorb PMo(12) selectively and thus be used for the determination of trace phosphorus. In a solution containing 2 mug ml(-1) phosphorus, the relative standard deviation is 4.69% (n=4), the peak height also varies linearly with the concentration of phosphorus over the range 0.4-25 mug ml(-1), and the detection limit is 0.04 mug ml(-1). The method is convenient and rapid. It has been used for the determination of inorganic phosphorus in phytic acid directly with satisfactory results.     

Automatic determination of cobalt at the submicrogram per millilitre level using a flowthrough spectrophotometric sensor

A flowthrough spectrophotometric sensor for the determination of cobalt at the nanogram per millilitre level using pyridoxal 4-phenylthiosemicarbazone as reagent and integrated preconcentration and detection in the flow cell is proposed. The method is highly selective for cobalt(II); it features detection and determination limits of 0.02 and 0.06 mug ml(-1) respectively, and a linear range of at least 0.04-18 mug ml(-1). The method is subject to very few interferences because the strongly acidic medium used prevents the formation of most complexes of the reagent with other metal ions. The method was applied to the determination of cobalt in pharmaceutical preparations.     

Flow injection spectrophotometric determination of trace amounts of selenium

A simple, rapid and sensitive flow injection spectrophotometric method for determination of selenium (0.005-1.5 mug ml(-1)) is described. The method is based on the catalytic effect of Se(IV) on the reduction reaction of thionine (TN) with sulphide ion, monitored spectrophotometrically at 598 nm. The detection limit is 5 ng ml(-1) the relative standard deviation for eight replicate measurements is 1.1% for 1 mug ml(-1) of selenium. The sampling rate is 25-30 samples h(-1). The procedure was applied successfully to the determination of selenium in real samples.     

Simultaneous determination of naproxen, salicylic acid and acetylsalicylic acid by spectrofluorimetry using partial least-squares (PLS) multivariate calibration

Determination of naproxen, salicylic acid and acetylsalicylic acid has been carried out in mixtures of up to three components by recording emission fluorescence spectra between 300 and 520 nm with an excitation wavelength of 290 nm. The excitation-emission spectra of these compounds are strongly overlapped, which does not permit their direct determination without previous separation by conventional methodologies. Here, a method is proposed for the determination of these chemicals by the use of a full-spectrum multivariate calibration method, partial least-squares (PLS). The experimental calibration matrix was designed with 18 samples. The concentrations were varied between 0.1 and 1.0 mug ml(-1) for naproxen, 0.5 and 5.0 mug ml(-1) for salicylic acid and from 2.0 to 12.0 mug ml(-1) for acetylsalicylic acid. The cross-validation method was used to select the number of factors. To check the accuracy of the proposed method, the optimized model, obtained using PLS-1, was applied to the determination of these compounds in pharmaceuticals and human serum samples previously spiked with different amounts of each chemical.     

A simple simultaneous flow injection method based on phosphomolybdenum chemistry for nitrate and nitrite determinations in water and fish samples

A direct spectrophotometric flow injection method for the simultaneous determination of nitrite and nitrate has been developed. The method is based on the oxidation of a phosphomolybdenum blue complex by the addition of nitrite and the decrease in absorbance of the blue complex is monitored at 820 nm. The injected sample is split into two segments. One of the streams was directly reacted with the above reagent and detected as nitrite. The other stream was passed through a copperised cadmium reductor column where reduction of nitrate to nitrite occurs, and the sample was then mixed with the reagent and passed through the cell of the spectrophotometer to be detected as nitrite plus nitrate. The conditions for the flow injection manifold parameters were optimised by experimental design and the concentration of nitrite and nitrate was determined in the linear range from 0.05 to 1.15 mug ml(-1) nitrite and 0.06 to 1.6 mug ml(-1) nitrate with a detection limit of 0.01 mug ml(-1) for nitrite and 0.025 mug ml(-1) for nitrate. The method is suitable for the simultaneous determination of nitrite and nitrate in fish and water samples with a sampling rate of 25+/-2 sample per hour.     

Katalytische bestimmung von silberspuren in wabetariger lösung und nach extraktion

The application of the catalysed oxidation of Bromopyrogallol Red by potassium per- sulphate for silver determination is discussed. In aqueous solution silver concentrations of 0.5- 1 mug/ml can be determined and 1- 13 ng/ml in the presence of 1, 10-phenanthroline as activator. In combination with solvent extraction, catalytic determination of the extracted silver is possible even in presence of 200 mug of iron(III), cobalt(II) and palladium(II). By means of an automatic variant of the simultaneous comparison method a more sensitive determination (0.2-20 ng/ml) was achieved.     

Fluorimetric determination of fluoride in a flow assembly integrated on-line to an open/closed FIA system to remove interference by solid phase extraction

A simple flow injection fluorimetric method for fluoride determination is proposed. The method is based on the enhanced fluorescence of quercitin-Zr(IV) complex when fluoride ion is present in the sample. An open/closed FIA manifold with a mini-column of Dowex 50W X8 resin was used to remove the most important interference (aluminum). The two FIA assemblies were integrated on-line to automate the pretreatment of the water sample and fluoride determination. The calibration graph was linear over the range 0.1-3.0 mug ml(-1) of fluoride with a correlation coefficient of 0.999 and LOD 0.06 mug ml(-1). The relative standard deviation was 2.5% and the sample throughput was 52 h(-1) without pretreatment and 10 h(-1) with pretreatment of the sample. The method was applied to the determination of fluoride in water samples.     

Malachite green as a reagent for detection and spectrophotometric determination of chromium(VI)

A sensitive and inexpensive method of spectrophotometric determination of chromium(VI), based on the absorbance of its complex with malachite green and acetic acid at pH 2.5 is reported. The complex shows a molar absorptivity of 8 x 10(4) l.mole(-1) cm(-1) at 560 nm, using malachite green and acetic acid as reference solution. The effect of time, temperature, pH and reagent concentration is studied and optimum operating conditions are established. Beer's law is applicable in the concentration range 2.0-22.8 mug/ml chromium(VI). The resin beads act as a catalyst and as little as 1.6 mug of chromium(VI) is detected in the resin phase as compared to 4.1 mug in the solution phase. The standard deviation in the determinations is +/-0.40 mug/ml for a 10.35 mug/ml solution.     

Flow injection analysis of nitrite by gas phase molecular absorption UV spectrophotometry

A flow injection method on the basis of gas phase molecular absorption is described for the determination of nitrite in the aqueous solution. 200 mul of nitrite solution is introduced into a carrier stream of distilled water. The carrier stream containing nitrite zone is reacted with a stream of hydrochloric acid (2 M). The stream is then segmented by O(2) gas. The produced gaseous products are purged into the O(2) segments, react with O(2) and are carried toward the gas-liquid separator. The gaseous phase is separated from the liquid stream by the use of home-made gas-liquid separator and then is swept into a home-made flow cell. The absorbance of gaseous phase is measured at 205 nm using a UV/VIS spectrophotometer. Under selected conditions, two linear ranges, up to 1000 mug ml(-1) and 1000-2000 mug ml(-1) of nitrite were obtained. The limit of detection was 7.5 mug ml(-1) NO(2)(-). The relative standard deviations of repeated measurements of 100 and 500 mug ml(-1) NO(2)(-) were 3.7 and 1.0%, respectively. Up to 30 samples h(-1) can be analyzed. Interferences in the proposed method were few and were readily overcome. The proposed method was successfully applied to the determination of nitrite in the spiked water samples, a number of meat products and urine.