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Biopharm Drug Dispos ; 43(1): 33-44, 2022 Feb.
Article in English | MEDLINE | ID: mdl-34997607

ABSTRACT

The study assessed the site dependent intestinal absorption of Daclatasvir and investigated the effects of piperine and omeprazole on such absorption utilizing in situ rabbit intestinal perfusion technique. The intestinal absorption of Daclatasvir was assessed in four segments: duodenum, jejunum, ileum, and colon. The effect of co-perfusion with omeprazole was monitored through the tested anatomical sites. The effect of piperine, a P-glycoprotein (P-gp) inhibitor on Daclatasvir absorption from jejunum and ileum was tested. The results showed that Daclatasvir was incompletely absorbed from the rabbit small and large intestine. The absorptive clearance per unit length (PeA/L) was site dependent and was ranked as colon > duodenum > jejunum > ileum. This rank is the opposite of the rank of P-gp intestinal content suggesting possible influence for P-gp. Co-perfusion with omeprazole increased PeA/L and this was evidenced also with reduced the L95% of Daclatasvir from both small and large intestinal segments. Significant enhancement in Daclatasvir absorption through jejunum and ileum was shown in presence of piperine. Daclatasvir showed site dependent intestinal absorption in a manner suggesting its affection by P-gp efflux. This effect was inhibited by piperine. Co-administration of Daclatasvir with omeprazole can enhance intestinal absorption a phenomenon which requires extension to human pharmacokinetic investigation.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1 , Omeprazole , ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Alkaloids , Animals , Benzodioxoles , Carbamates , Ileum/metabolism , Imidazoles , Intestinal Absorption , Intestines , Jejunum/metabolism , Omeprazole/pharmacology , Piperidines , Polyunsaturated Alkamides , Pyrrolidines , Rabbits , Valine/analogs & derivatives
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