RESUMEN
An affinity sensor based on capacitive transduction was developed to detect a model compound, metergoline, in a continuous flow system. This system simulates the monitoring of low-molecular weight organic compounds in natural flowing waters, i.e. rivers and streams. During operation in such scenarios, control of the experimental parameters is not possible, which poses a true analytical challenge. A two-step approach was used to produce a sensor for metergoline. Submicron spherical molecularly imprinted polymers, used as recognition elements, were obtained through emulsion polymerization and subsequently coupled to the sensor surface by electropolymerization. This way, a robust and reusable sensor was obtained that regenerated spontaneously under the natural conditions in a river. Small organic compounds could be analyzed in water without manipulating the binding or regeneration conditions, thereby offering a viable tool for on-site application.
Asunto(s)
Electroquímica/instrumentación , Metergolina/análisis , Impresión Molecular/métodos , Polímeros/química , Contaminantes Químicos del Agua/análisis , Agua/química , Capacidad Eléctrica , Monitoreo del Ambiente/instrumentación , Diseño de Equipo , Análisis de Falla de Equipo , Propiedades de Superficie , TransductoresRESUMEN
Observation of a potentiometric sensor's response behaviour after injection in flow injection analysis at different concentrations allowed studying "on" and "off" kinetics of the analyte's adsorption/diffusion behaviour. The alkaloid metergoline was mostly used as an example. k(on) and k(off) rate constant values were measured, and the association constant K(ass), and ΔG values of the analyte-surface interaction were calculated with an adsorption-based model which proved to be fully applicable. k(on) increased by decreasing the sensor dimensions, while koff was unaffected by miniaturization. Increasing acetonitrile concentrations in the running buffer increased k(off), while k(on) was unaffected. The experimentally determined ΔG values of the analyte-surface interaction showed a linear relation to the response of the sensor, in mV. This knowledge was applied to optimize the potentiometric detection of plant alkaloids in (U)HPLC. Sub-micromolar detection limits were obtained with the potentiometric detector/(U)HPLC combination. This is the first time that the response rates and the response itself can be modelled accurately for coated wire potentiometric sensors, and it is the first application of a potentiometric detector in UPLC.
Asunto(s)
Cromatografía Líquida de Alta Presión , Potenciometría , Acetonitrilos/análisis , Adsorción , Alcaloides/análisis , Cocaína/análisis , Diosgenina/análisis , Cinética , Metergolina/análisis , Modelos Químicos , Papaverina/análisis , Plantas/química , Potenciometría/instrumentaciónRESUMEN
Ergot alkaloids are mycotoxins produced by fungi of the genus Claviceps, which infect cereal crops and grasses. The uptake of ergot alkaloid contaminated cereal products can be lethal to humans and animals. For food safety assessment, analytical techniques are currently used to determine the presence of ergot alkaloids in food and feed samples. However, the number of samples which can be analyzed is limited, due to the cost of the equipment and the need for skilled personnel. In order to compensate for the lack of rapid tests for the detection of ergot alkaloids, the aim of this study was to develop a specific recognition element for ergot alkaloids, which could be further applied to produce a colorimetric reaction in the presence of these toxins. As recognition elements, single-stranded DNA ligands were selected by using an iterative selection procedure named SELEX, i.e., Systematic Evolution of Ligands by EXponential enrichment. After several selection cycles, the resulting aptamers were cloned and sequenced. A surface plasmon resonance analysis enabled determination of the dissociation constants of the complexes of aptamers and lysergamine. Dissociation constants in the nanomolar range were obtained with three selected aptamers. One of the selected aptamers, having a dissociation constant of 44 nM, was linked to gold nanoparticles and it was possible to produce a colorimetric reaction in the presence of lysergamine. This system could also be applied to small ergot alkaloids in an ergot contaminated flour sample.
Asunto(s)
Aptámeros de Nucleótidos/química , Grano Comestible/química , Alcaloides de Claviceps/análisis , Análisis de los Alimentos/métodos , Metergolina/análisis , Micotoxinas/análisis , Oro/química , Nanopartículas del Metal/químicaRESUMEN
The structure of some 1,6-dimethyl-12-hydroxy-10alpha-ergoline derivatives, related to an active metabolite of metergoline, is established by using physical methods (mass spectrometry, electronic and fluorescence spectroscopy, and 1H N.M.R. spectroscopy). The 13C N.M.R. spectrum of compound (II), 1,6-dimethyl-8beta-(acetylaminomethyl)-12-hydroxy-10alpha-ergoline, is analyzed.