Innovative design of a methodology for the simultaneous determination of compounds by kinetic-spectroscopy three-dimensional chemiluminescence.

This report presents a novel methodology based in the quickly acquisition of full UV-vis range spectra combined with the joint determination of kinetic parameters and chemiluminescence signals. Then this technique allows obtaining three-dimensional chemiluminescence spectra profiles containing kinetic and spectroscopic information. That is especially useful for resolving mixtures of luminophors because of more analytical information for each analyte is available increasing the selectivity relative to conventional chemiluminescence methods. To accomplish this, a conventional Back-Thinned CCD detector is used and the three-dimensional chemiluminescence spectra is subsequently processed so that two-dimensional spectra with different trajectories can be obtained by dedicated software CLTotal. The potential of the proposed analytical methodology was assessed for the simultaneous determination of two polycyclic aromatic hydrocarbons. The chemiluminescent reaction between DNPO and hydrogen peroxide induced by their presence was used to record 3D spectra and the software CLTotal to subsequently construct linear variable-angle trajectories in the spectra, in order to obtain more selective 2D spectra facilitating the simultaneous determination of the analytes. The results of the statistical analysis testify to the usefulness of the proposed method for the intended purpose.

Flow injection chemiluminescence determination of vitamin B12 using on-line UV-persulfate photooxidation and charge coupled device detection.

A sensitive chemiluminescence method for vitamin B(12) using a charge-coupled device (CCD) photodetector combined with on-line UV-persulfate oxidation in a simple continuous flow system has been developed. The principle for the determination of vitamin B(12) is based on the enhancive effect of cobalt (II) on the chemiluminescence reaction between luminol and percarbonate in alkaline medium. In addition, percarbonate has been investigated and proposed as a powerful source of hydrogen peroxide as oxidant agent in this chemiluminescence reaction. The digestion of vitamin B(12) to release the cobalt (II) is reached by UV irradiation treatment in a persulfate medium. The CCD detector, directly connected to the flow cell, is used with the continuous flow manifold to obtain the full spectral characteristics of cobalt (II) catalyzed luminol-percarbonate reaction. The vitamin B(12) oxidation process and chemical conditions for the chemiluminescence reaction were investigated and optimized. The increment of the emission intensity was proportional to the concentration of vitamin B(12) , giving a second-order calibration graph over the cobalt (II) concentration range from 10 to 5000 µg L(-1)(r(2) = 0.9985) with a detection limit of 9.3 µg L(-1). The proposed method was applied to the determination of vitamin B(12) in different kinds of pharmaceuticals.

Simultaneous stopped-flow determination of morphine and naloxone by time-resolved chemiluminescence.

The first application of the flow analysis coupled with chemiluminescence detection and based on stopped-flow chemistry to the simultaneous determination of two components, using a two equation system, is described. The proposed method to determine simultaneously morphine and naloxone is based on the chemiluminescence oxidation of these compounds by their reaction with potassium permanganate in an acidic medium. The main feature of the system used is that the recording of the whole chemiluminescence intensity-versus-time profiles can be obtained, using the stopped-flow technique in a continuous-flow system. Then, the chemiluminescent signals obtained at two times of these profiles can be used to determine the concentration of both opiate narcotics. The effect of common emission enhancers on the chemiluminescence emission of these compounds in different acidic media, using the above-mentioned technique, was studied, in order to achieve the best conditions in which, the CL profiles of both compounds should be additive. The parameters selected were sulphuric acid 1.0 mol L(-1), permanganate 0.2 mmolL(-1) and formaldehyde 0.8 mol L(-1). Taken in account the different profiles of the transient CL signal obtained with each compounds, using the selected chemical conditions, two measurement times (1.4 and 4.8s) of these responses curves were considered with the purpose to establish a simple 2 x 2 matrix calculation. Using the chemiluminiscent signals obtained at these times, a linear calibration graph was obtained for each one of the compounds between 0.01 and 1.00 mg L(-1) for morphine and 0.10-1.50 mg L(-1) for naloxone. The present chemiluminescence procedure was applied to the determination of both compounds in mixtures and was found to be satisfactory.

Multivariate calibration applied to the time-resolved chemiluminescence for the simultaneous determination of morphine and its antagonist naloxone.

A novel alternative for the simultaneous determination of compounds with similar structure is described, using the whole chemiluminescence-time profiles, acquired by the stopped-flow technique, in combination with mathematical treatments of multivariate calibration. The proposed method is based on the chemiluminescent oxidation of morphine and naloxone by their reaction with potassium permanganate in an acidic medium, using formaldehyde as co-factor. The whole chemiluminescence-time profiles, acquired using the stopped-flow technique in a continuous-flow system, allowed the use of the time-resolved chemiluminescence (CL) data in combination with multivariate calibration techniques, as partial least squares (PLS), for the quantitative determination of both opiate narcotics in binary mixtures. In order to achieve overcoat the additivity of the CL profiles and beside to obtain CL profiles for each drug the most separated as possible in the time, the optimum chemical conditions for the CL emission were investigated. The effect of common emission enhancers on the CL emission obtained in the oxidation reaction of these compounds in different acidic media was studied. The parameters selected were sulphuric acid 1.0 mol L(-1), permanganate 0.2 mmol L(-1) and formaldehyde 0.8 mol L(-1). A calibration set of standard samples was designed by combination of a factorial design, with three levels for each factor and a central composite design. Finally, with the aim of validating the chemometric proposed method, a prediction set of binary samples was prepared. Using the multivariate calibration method proposed, the analytes were determined in synthetic samples, obtaining recoveries of 97-109%.