Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Curr Drug Deliv ; 15(3): 367-387, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29219056

RESUMO

BACKGROUND: Polysaccharide based delivery systems have been successfully used to target drugs to colon. In some recent reports, the superiority of concomitant administration of probiotics with such systems has been established. However, the pharmacokinetics of such symbiotic therapy remain unexplored hitherto. METHODS: This study deciphers the pharmacokinetic parameters of guar gum based colon targeted spheroids of sulfasalazine with co-administration of probiotics in experimental rats. Thirty rats were divided into five groups using Latin square design. These were subjected to treatment with delayed release formulation, uncoated spheroids, coated spheroid and coated spheroids along with probiotics. RESULTS: In case of delayed release formulation, negligible presence of sulfasalazine in plasma was observed in first 2h, followed by significant increase in sulfasalazine concentration after 3h. Higher plasma concentrations of sulfasalazine were detected for uncoated spheroids with and without probiotics. Negligible release of drug upto 5h and delayed Tmax in case of guar-gum coated sulfasalazine spheroids with or without probiotics clearly indicated successful formulation of colon targeted spheroids. Further, for coated spheroids (both with and without probiotics), the value of Tmax is found to be significantly higher than those with the other treatments. CONCLUSION: Colon targeted spheroids were therefore, found to reduce absorption of drug which, in turn, is expected to reduce the side effects as only local action in colon is required for treatment of colitis. This is the first report on pharmacokinetic study of a colon targeted delivery system co-administered with probiotics.


Assuntos
Colo/metabolismo , Sistemas de Liberação de Medicamentos , Galactanos/administração & dosagem , Fármacos Gastrointestinais/administração & dosagem , Mananas/administração & dosagem , Gomas Vegetais/administração & dosagem , Ácidos Polimetacrílicos/administração & dosagem , Probióticos/administração & dosagem , Sulfassalazina/administração & dosagem , Animais , Preparações de Ação Retardada/administração & dosagem , Preparações de Ação Retardada/química , Preparações de Ação Retardada/farmacocinética , Feminino , Galactanos/química , Galactanos/farmacocinética , Fármacos Gastrointestinais/química , Fármacos Gastrointestinais/farmacocinética , Masculino , Mananas/química , Mananas/farmacocinética , Gomas Vegetais/química , Gomas Vegetais/farmacocinética , Ácidos Polimetacrílicos/química , Ácidos Polimetacrílicos/farmacocinética , Probióticos/química , Probióticos/farmacocinética , Ratos Sprague-Dawley , Sulfassalazina/química , Sulfassalazina/farmacocinética
2.
J Adv Pharm Technol Res ; 8(4): 150-155, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29184847

RESUMO

To overcome the limitations of the conventionally used methods for evaluation of orally administered colon-targeted delivery systems, a novel dissolution method using probiotics has been recently reported. In the present study, universal suitability of this medium composed of five different probiotics is established. Different delivery systems - mini tablets, liquisolid compacts, and microspheres coated with different polysaccharides - were prepared and subjected to sequential dissolution testing in medium with and without microbiota. The results obtained from fluid thioglycollate medium (FTM)-based probiotic medium for all the polysaccharide-based formulations showed statistically similar dissolution profile to that in the rat and goat cecal content media. Hence, it can be concluded that the developed FTM-based probiotic medium, once established, may eliminate the need for further animal sacrifice in the dissolution testing of polysaccharide-based colon-targeted delivery system.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...