RESUMEN
The endocrine disruptor metoprolol has been oxidised in aqueous solution by means of the systems UV-C, UV-C/H(2)O(2), UV-C/percarbonate, UV-C/monopersulfate, UV-C/TiO(2), UV-C/H(2)O(2)/TiO(2) and photo-Fenton. From simple photolysis experiments the quantum yield of metoprolol has been calculated (roughly 5x10(-3) mol Einstein(-1) at circumneutral pH). Addition of free radicals promoters significantly enhanced the metoprolol depletion rate. Mineralization degree was negligible when no promoter was added, while low values were achieved in the presence of either inorganic peroxides or titanium dioxide. The combination of radiation, hydrogen peroxide and TiO(2) increased the mineralization level up to values in the proximity of 45-50% under the best conditions investigated. The photo-Fenton process was the best system in terms of total oxidation (mineralization degree 70%) when optimum conditions were applied.
Asunto(s)
Antagonistas Adrenérgicos beta/efectos de la radiación , Metoprolol/efectos de la radiación , Contaminantes Químicos del Agua/efectos de la radiación , Antagonistas Adrenérgicos beta/química , Algoritmos , Carbonatos/química , Catálisis , Radicales Libres/química , Peróxido de Hidrógeno , Hierro , Metoprolol/química , Peróxidos/química , Fotólisis , Titanio/química , Rayos Ultravioleta , Contaminantes Químicos del Agua/química , Purificación del AguaRESUMEN
DNA vaccination using plasmid encoding the hemagglutinin (HA) gene of influenza A/PR/8/34 virus to induce long-lasting protective immunity against respiratory infection was evaluated in this study. Using liposomes as carriers, the efficacy of DNA vaccines was determined using a lethal influenza infection model in mice. Mice immunized intranasally or intramuscularly with liposome-encapsulated pCI plasmid encoding HA (pCI-HA10) were completely protected against an intranasal 5 LD(50) influenza virus challenge. Mice immunized with liposome-encapsulated pCI-HA10, but not naked pCI-HA10, by intranasal administration were found to produce high titers of serum IgA. These results suggest DNA vaccines encapsulated in liposomes are efficacious in inducing complete protective immunity against respiratory influenza virus infection.