Your browser doesn't support javascript.
loading
Transport of aripiprazole across Caco-2 monolayer model / 药学学报
Acta Pharmaceutica Sinica ; (12): 188-191, 2009.
Article in Zh | WPRIM | ID: wpr-410152
Responsible library: WPRO
ABSTRACT
This study aimed to investigate the transport characteristics of aripiprazole.A human intestinal epithelial cell model Caco-2 cell in vitro cultured had been applied to study the transport of aripiprazole.The effects of time,concentration of donor solutions,pH,temperature and P-glycoprotein inhibitor on the transport of aripiprazole were investigated.The determination of aripiprazole was performed by HPLC.It is concluded that aripiprazole is transported through the intestinal mucosa via a passive diffusion mechanism primarily,coex- isting with a carrier-mediated transport.The transport of aripiprazole is positively correlated to transport time, concentrations.The P-glycoprotein inhibitor cyclosporine A significantly enhanced the transport amount of aripiprazole.
Key words
Full text: 1 Index: WPRIM Type of study: Prognostic_studies Language: Zh Journal: Acta Pharmaceutica Sinica Year: 2009 Type: Article
Full text: 1 Index: WPRIM Type of study: Prognostic_studies Language: Zh Journal: Acta Pharmaceutica Sinica Year: 2009 Type: Article