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1.
Water Res ; 47(5): 1803-15, 2013 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-23351432

RESUMEN

The electrochemical incineration of omeprazole, a widely prescribed gastrointestinal drug which is detected in natural waters, has been studied in a phosphate buffer of pH 7.0 by anodic oxidation with electrogenerated H(2)O(2) (AO-H(2)O(2)) operating at constant current density (j). The experiments were carried out in a cell equipped with either a Pt or a boron-doped diamond (BDD) anode and an air-diffusion cathode to continuously produce H(2)O(2). In these systems, organics are mainly oxidized by hydroxyl radicals formed at the Pt or BDD surface from water oxidation. A partial total organic carbon (TOC) abatement close to 78% for omeprazole was achieved by AO-H(2)O(2) with a BDD anode after consumption of 18 Ah L(-1) at 100 mA cm(-2), whereas the alternative use of Pt did not allow mineralizing the drug. However, the drug was totally removed using both anodes, although it decayed more rapidly using BDD. In this latter system, increasing j accelerated the degradation process, but lowering the mineralization current efficiency. Greater drug content also enhanced the degradation rate with higher mineralization degree and current efficiency. The kinetics for omeprazole decay always followed a pseudo-first-order reaction and its rate constant increased with increasing j and with decreasing its concentration. Seven heteroaromatic intermediates and four hydroxylated derivatives were detected by LC-MS, while nine short-linear carboxylic acids were identified and quantified by ion-exclusion HPLC. These acids were largely accumulated using Pt and rapidly removed using BDD, thus explaining the partial mineralization of omeprazole achieved by AO-H(2)O(2) with the latter anode. The release of inorganic ions such as NO(3)(-), NH(4)(+) and SO(4)(2-) was followed by ionic chromatography. A plausible reaction sequence for omeprazole mineralization involving all intermediates detected is proposed.


Asunto(s)
Boro/química , Diamante/química , Electroquímica/métodos , Incineración/métodos , Omeprazol/aislamiento & purificación , Platino (Metal)/química , Agua/química , Aire , Carbono/análisis , Ácidos Carboxílicos/análisis , Difusión , Electricidad , Electrodos , Peróxido de Hidrógeno/química , Iones , Cinética , Minerales/química , Nitrógeno/análisis , Omeprazol/análisis , Omeprazol/química , Compuestos Orgánicos/análisis , Oxidación-Reducción , Soluciones , Sulfatos/análisis , Factores de Tiempo
2.
J Chromatogr A ; 1162(1): 97-102, 2007 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-17645885

RESUMEN

Chromatographic separation of the chiral drugs rolipram, bupivacaine and omeprazole on a tartardiamide-based stationary phase commercially named Kromasil CHI-TBB is shown in this work. The effect of temperature on the chromatographic separation of the chiral drugs using the Kromasil CHI-TBB stationary phase was determined quantitatively so as to contribute toward the design for the racemic mixtures of the named compound by using chiral columns. A decrease in the retention and selectivity factors was observed, when the column temperature increased. Van't Hoff plots provided the thermodynamic data. The variation of the thermodynamic parameters enthalpy and entropy are clearly negative meaning that the separation is enthalpy controlled.


Asunto(s)
Bupivacaína/aislamiento & purificación , Cromatografía Líquida de Alta Presión/métodos , Cromatografía por Intercambio Iónico/métodos , Omeprazol/aislamiento & purificación , Rolipram/aislamiento & purificación , Tartratos/química , Algoritmos , Resinas de Intercambio Aniónico , Bupivacaína/química , Fenómenos Químicos , Química Física , Modelos Químicos , Estructura Molecular , Omeprazol/química , Rolipram/química , Estereoisomerismo , Temperatura , Termodinámica
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