ABSTRACT
The determination of thiamine was carried out by UV-photodegradation in a single-line flow-injection assembly. The UV-photodegradation of thiamine was carried out in the coil of the injection valve, constituted of a PTFE tubing, half of its length being helically coiled around a UV lamp. A peak with two adjoining maxima was produced by injection, corresponding to the absorbance of the irradiated and non-irradiated sample. The analytical parameter is the difference between the two peaks, measured at 264 nm. The calibration graph is linear over the 1.2-30 mug/ml range of thiamine hydrochloride in 0.1M HCl. The influence of certain admixed substances was studied and the method was tested for the determination of thiamine in tablets.
ABSTRACT
The partition constants of Cadion, i.e., 1-(p-nitro-phenyl)-3-(p'-azobenzene)-triazene, of its complex with the methylmercuric ion, and of methylmercury chloride were determined in the system toluene/aqueous phase containing 40 vol.% methyl alcohol; they have the values of 4.3 x 10(3), 3.0 x 10(3), and 2.6 respectively. The reagent has an absorption maximum at 406 nm, whereas the methylmercury complex at 460 nm. The K(HR) value corresponding to the H(+) + R(-) right harpoon over left harpoon HR equilibrium is 10(10.85), HR being the reagent molecule and H belongs to the NH of the triazenic group (NNNH). The K(ext) value corresponding to the equilibrium H(3)CHg(+) + (HR)(o) right harpoon over left harpoon (H(3)CHgR)(o) + H(+) is 1.0, where the "o" indicates the species present in the organic phase. The reagent/H(3)CHg(+) combination ratio is 1/1. The formation constant of the methylmercury complex, K(H(3)CHgR), which corresponds to the equilibrium H(3)CHg(+) + R(-) right harpoon over left harpoon H(3)CHgR, has a value of 10(10.8) as estimated by means of two different methods. The IR spectra allowed some conclusions to be drawn concerning the formation of the complex. The complex is stable up to 180 degrees , and the reagent up to 140 degrees . The molar absorptivity is of 3.46 x 10(4) 1.mole(-1).cm(-1) and the H(3)CHg(+) can be determined in the range 0.025-4 ppm. The determination is highly selective.
ABSTRACT
The reaction between Hg(II) and Cadion A and Cadion 2B has been studied. Methods are suggested for the determination of Hg(II) in the 0.1-4 ppm range with Cadion A and in the 0.2-8 ppm range with Cadion 2B. Of the 49 ions studied only Hg(I), Sn(II), Br(-), I(-), MnO(-)(4), EDTA, SCN(-), CN(-) and S(2-) interfere. The combination ratios and instability constants of the Hg-Cadion complexes were determined. The structural formulae of the complexes were deduced from the infrared spectra and elemental and thermogravimetric analyses.
ABSTRACT
A simple, selective and rapid method for determination of ascorbic acid from fruit juices was developed by combining a flow injection analysis (FIA) system with a chemiluminometric detector and a reactor with L-ascorbate oxidase immobilized on controlled pore glass. It was found that some reducing agents (eg ascorbic acid and mercaptoacetic acid) give chemiluminescence with luminol in the presence of hexacyanoferrate (III) in an alkaline solution. We used this new type of chemiluminescent reaction for the enzymatic determination of ascorbic acid. The background substraction method was used in order to avoid interference during ascorbic acid determination. Accordingly, two chemiluminometric signals were registered for each determination, one signal corresponding to the sample that passed through the enzymatic reactor that decomposed the ascorbic acid completely, and the second signal corresponding to the sample that does not pass through the reactor. The difference between the two signals corresponds to ascorbic acid from the sample. The linear range of the method was 10-1000 micromol/L of ascorbic acid and the detection limit was 5 micromol/L The throughput was four samples/h and RSD 3.13% (n = 10). This method was applied for determination of ascorbic in fruit juices. The results were compared with those found by the reference method, based on titrimetric determination with 2,6-dichlorophenolindophenol, and the concordance was excellent.
Subject(s)
Ascorbate Oxidase , Beverages/analysis , Enzymes, Immobilized , Citrus , Equipment Design , Ferricyanides , Flow Injection Analysis/instrumentation , Flow Injection Analysis/methods , Fruit , Indicators and Reagents , Luminescent Measurements , LuminolABSTRACT
A highly sensitive flow analysis method for determination of acetylcholinesterase (AChE) inhibitors like organophosphorous pesticides using a new chemiluminescent reaction was developed and optimized. This method is fast, sensitive, and cheap, because it requires only one enzyme and its substrate. The system incorporates a reactor with immobilized AChE on controlled pore glass (CPG) and a chemiluminometric detector. Variations in enzyme activity due to inhibition are measured from the changes of concentrations of thiocholine produced when the substrate (acetylthiocholine chloride) is pumped before and after the passage of the solution containing the pesticide through the immobilized AChE reactor. Thiocholine is determined by a new chemiluminescent reaction with luminol in the presence of potassium ferricyanide. The percentage inhibition of enzyme activity is correlated to the pesticide concentration. The inhibited enzyme is reactivated by 10 mM pyridine-2-aldoxime methiodide (2-PAM). The experimental conditions were first optimized for activity determination of the effect of pH, flow rates, and Tris concentrations. For the measurement of AChE inhibition, the appropriate concentration of the substrate is selected such that the rate of noninhibited reaction can be considered unchanged and could be used as a reference. For optimization of experimental conditions for inhibition, several parameters of the system are studied and discussed: flow rate, enzyme-pesticide contact time, luminol concentration, ferricyanide concentration, 2-PAM concentration, and configuration of the FIA manifold. Paraoxon, an organophosphorous pesticide was tested. For an inhibition time of 10 min the calibration graph is linear from 0.1 to 1 ppm paraoxon with a relative standard deviation (n = 5) of 4.6% at 0.5 ppm. For an inhibition time of 30 min the calibration graph is linear from 25 to 250 ppb paraoxon.