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Influence of piperine and omeprazole on the regional absorption of Daclatasvir from rabbit intestine.
Ashmawy, Shimaa M; Eltahan, Dina A; Osman, Mohamed A; Essa, Ebtessam A.
Afiliación
  • Ashmawy SM; Department of Pharmaceutical Technology, College of Pharmacy, University of Tanta, Tanta, Egypt.
  • Eltahan DA; Department of Pharmaceutical Technology, College of Pharmacy, University of Tanta, Tanta, Egypt.
  • Osman MA; Department of Pharmaceutical Technology, College of Pharmacy, University of Tanta, Tanta, Egypt.
  • Essa EA; Department of Pharmaceutical Technology, College of Pharmacy, University of Tanta, Tanta, Egypt.
Biopharm Drug Dispos ; 43(1): 33-44, 2022 Feb.
Article en En | 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Omeprazol / Miembro 1 de la Subfamilia B de Casetes de Unión a ATP Límite: Animals Idioma: En Revista: Biopharm Drug Dispos Año: 2022 Tipo del documento: Article País de afiliación: Egipto

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Omeprazol / Miembro 1 de la Subfamilia B de Casetes de Unión a ATP Límite: Animals Idioma: En Revista: Biopharm Drug Dispos Año: 2022 Tipo del documento: Article País de afiliación: Egipto