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Biomedical subjects

M Lores

Publications and source records attributed to M Lores.

8 recordsLinked to original sources

Computer-assisted transfer of programmed elutions in reversed-phase high-performance liquid chromatography.

Computer-assisted procedures were used to simulate modifications in chromatograms caused by the transfer of elution programmes between instruments with significantly different dwell volumes. Moreover, for the first time the same approach was used to modify the elution programmes to match the chromatograms produced in the different instruments. The process may consist of making minor modifications to gradient programmes or transforming the original gradient programme into a stepwise gradient profile and/or the simultaneous programming of flow and solvent composition. The combination of these approaches has been shown to have an enormous potential for producing matched chromatograms in instrumental systems with dwell volumes that differ by several millilitres. The efficiency and robustness of the proposed procedure is demonstrated with a variety of compounds (two different mixtures of 10 and 11 analytes), mobile phases (methanol and acetonitrile gradients), flow rates (0.5-1.5 mL/min range), temperatures (35-45 degrees C interval) and gradient profiles (linear, multilinear, curved and stepwise).

Acetonitriles↗

Photochemical studies of a polybrominated diphenyl ethers (PBDES) technical mixture by solid phase microextraction (SPME).

In this work the photochemical behaviour of a technical mixture of polybrominated diphenyl ethers (PBDEs) (BDE-47, BDE-99, BDE-100, BDE-153 and BDE-154) has been studied. The mixture of BDEs was extracted from aqueous solutions using SPME fibers that were subsequently exposed to different UV irradiation times, procedure so-called Photo-SPME. PBDEs photochemical studies in such medium have been accomplished for the first time. Twenty one different photoproducts, all of them generated by successive bromine atoms losses, have been identified, being their photoformation-photodegradation curves easily determined by the Photo-SPME technique.

Bromine↗

Further solid-phase microextraction-gas chromatography-mass spectrometry applications: "on-fibre" and aqueous photodegradation of nitro musks.

Photodegradation kinetics of four nitro musks (musk xylene, musk tibetene, musk ketone and musk moskene) in solid-phase microextraction (SPME) fibres ("photo-SPME") and in an aqueous system were studied by means of gas chromatography-mass spectrometry (MS) detection. Musks fragrances were extracted from aqueous solutions using SPME fibres that subsequently were exposed to different UV irradiation times, generating photoproducts easily characterized by their mass spectra. Aqueous photodegradation studies followed by SPME were also performed and compared to photo-SPME. The same fourteen photoproducts have been detected in both media. The potential of this approach to readily calculate apparent rate constants (from 10(-4) to 10(-3) s(-1)), half-life times (from 3 to 32 min) and reaction orders (n = 1) in both media is stated. The main photoreaction determined was photocyclization, but products of photoreduction and photorearrangement have also been detected. Tentative photodegradation pathways for musk moskene and musk tibetene are proposed for the first time.

Gas Chromatography-Mass Spectrometry↗

Simultaneous determination of neutral and acidic pharmaceuticals in wastewater by high-performance liquid chromatography-post-column photochemically induced fluorimetry.

An analytical method for the simultaneous determination of acidic and neutral pharmaceutical active compound (PhACs) residues in wastewater has been developed based on the combination of high-performance liquid chromatography (HPLC) and photochemically induced fluorimetry. The photoderivatization conditions for each particular PhAC have been assessed. Off-line optimization of the HPLC separation for both neutral and acidic compounds has been utilised and evaluated. Detection limits in the low ng/ml range have been achieved without sample pretreatment. By applying the developed analytical method combined with solid-phase extraction to real wastewater samples an enrichment factor of approximately two orders of magnitude can be obtained.

Chromatography, High Pressure Liquid↗

Photolysis of polychlorinated biphenyls by solid-phase microextraction. "On-fibre" versus aqueous photodegradation.

The photodegradation kinetics of polychlorinated biphenyls "on-fibre" is described. The utilisation of solid-phase microextraction (SPME) fibres to monitor photolysis pathways and determine photoproducts constitutes a new approach that exploits the solvent-free aspect and concentration possibilities of this technique. Direct photolysis of aqueous solutions containing polychlorinated biphenyls (PCBs) was also undertaken and SPME was used in this case for photoproduct extraction purposes. Reductive dechlorination was the main decomposition mechanism in both procedures. Less-chlorinated biphenyls are the principal photoproducts and, among these, some toxic coplanar species have been detected. The influence of irradiation time was evaluated for both treatments. SPME was found to be a good choice for the extraction of photoproducts in experiments conducted in the classical way (extraction after photolysis). Moreover, it is demonstrated that photolysis of PCBs "on fibre" is realistic and provides the possibility of evaluating the phototransformation of these pollutants at environmental levels.

Mass Spectrometry↗

On-fibre photodegradation studies of polychlorinated biphenyls using SPME-GC-MS-MS: a new approach.

The known advantages of solid-phase microextraction as a simple, one-step, rapid and solvent free extraction technique are exploited to study the photodegradation kinetics of polychlorinated biphenyls "on-fibre". The obtained results show the possibilities of this new approach not only to monitor the photolysis pathways of such compounds but to determine the photoproducts produced at different irradiation times and/or wavelengths. Photoproducts of PCB decomposition were less chlorinated biphenyls, among them some coplanar congeners have been found, which is important from a toxicological point of view.

Environmental Pollutants↗

Optimisation of alachlor solid-phase microextraction from water samples using experimental design.

We have tested screening and response surface experimental designs to optimise the solid-phase microextraction (SPME) of the widely used herbicide alachlor. Extraction time and sample volume were the only statistically significant factors from those studied. In the final optimised conditions the procedure was applied to the SPME-HPLC analysis of alachlor in spiked water samples with excellent figures of merit.

Acetamides↗

Analysis of barbiturates by micro-high-performance liquid chromatography with post-column photochemical derivatization.

This study attempts to combine the advantages of microcolumn high-performance liquid chromatography (micro-HPLC) with those of post-column photochemical derivatization in barbiturate analysis. Some barbiturates are photochemically unstable, leading to photoproducts that show maximum absorption at 270 nm and not the typical one at approximately 220 nm. For this purpose, a laboratory-built photoreactor has been developed to work with micro-HPLC instruments. Its performance is satisfactory in the forensic analysis of barbiturates.

Barbiturates↗