RESUMO
Near-infrared absorption of strontium titanate (SrTiO3) doped with rhodium (Rh) was investigated by photoacoustic (PA) Fourier transform infrared spectroscopy. In the absence of an electron acceptor and the presence of a hole scavenger, the largest absorption change in the Rh valence state from tetravalent to trivalent was observed in Rh-doped SrTiO3 prepared at 1473 K, which showed the highest activity for hydrogen evolution. PA measurements revealed the effective redox cycle mechanism between tetravalent and trivalent Rh ions in Rh-doped SrTiO3.
RESUMO
Mid-infrared absorption of titanium(iv) oxide (TiO2) under ultraviolet (UV) irradiation was studied by Fourier transform infrared spectroscopy using a photoacoustic (PA) technique. UV irradiation induced an upward shift of the PA spectra, which is due to the trivalent titanium (Ti3+) species produced by electron accumulation. The PA spectra under UV irradiation mainly depend on the crystal structure, indicating that the energy levels of Ti3+ are largely determined by crystal structures.
RESUMO
The objective of the present study was to determine the optimum composition for sustained-release of tamsulosin hydrochloride from microparticles intended for orally disintegrating tablets. Microparticles were prepared from an aqueous ethylcellulose dispersion (Aquacoa®), and an aqueous copolymer based on ethyl acrylate and methyl methacrylate dispersion (Eudragit®) NE30D), with microcrystalline cellulose as core particles with a fluidized bed coating process. Prepared microparticles were about 200 µm diameter and spherical. The microparticles were evaluated for in vitro drug release and in vivo absorption to assess bioequivalence in a commercial product, Harnal® pellets. The optimum ratio of Aquacoat® and Eudragit® NE30D in the matrix was 9:1. We observed similar drug release profiles in microparticles and Harnal® pellets. Higuchi model analysis of the in vitro drug release from microparticles was linear up to 80% release, typical of Fickian diffusion sustained-release profile. The in vivo absorption properties from microparticles were comparable to Harnal® pellets, and there was a linear relationship between in vitro drug release and in vivo drug release. In conclusion, this development produces microparticles in single-step coating, that provided a sustained-release of tamsulosin hydrochloride comparable to Harnal® pellets.
Assuntos
Antagonistas de Receptores Adrenérgicos alfa 1/química , Celulose/química , Composição de Medicamentos/métodos , Excipientes/química , Sulfonamidas/química , Administração Oral , Antagonistas de Receptores Adrenérgicos alfa 1/administração & dosagem , Antagonistas de Receptores Adrenérgicos alfa 1/farmacocinética , Animais , Celulose/análogos & derivados , Química Farmacêutica , Cromatografia Líquida , Preparações de Ação Retardada , Cães , Masculino , Metacrilatos/química , Microesferas , Modelos Químicos , Tamanho da Partícula , Polímeros/química , Solubilidade , Sulfonamidas/administração & dosagem , Sulfonamidas/farmacocinética , Comprimidos com Revestimento Entérico , Tansulosina , Espectrometria de Massas em Tandem , Equivalência TerapêuticaRESUMO
Gastric pH is an important factor which significantly affects the dissolution of drugs, and therefore their bioavailability. In this study, the gastric pHs were measured directly with a miniature pH electrode inserted through the nostril into the body of the stomach of cynomolgus monkeys. Results from three separate sets of measurements using the same male monkeys indicated that the median gastric pH profiles of unfed monkeys were low, fluctuating between pH 1 and pH 3. However, the median gastric pHs in fed monkeys given about 108 g of a biscuit-type solid food, which are commonly provided, shifted toward a more neutral range between pH 5 and pH 7, and remained in this range for about 9 h. This result contrasted with reported results for humans after eating a standard meal, which showed a neutral range between pH 5 and pH 7 for a brief period. Consequently, these results indicate that although the gastric pH of unfed cynomolgus monkeys is similar to that of fasting humans, there is a great difference in the gastric pH profiles between humans and monkeys after eating, which suggests that further studies are needed to establish optimal feeding conditions for bioavailability studies in monkeys.