Segmental-dependent permeability throughout the small intestine following oral drug administration: Single-pass vs. Doluisio approach to in-situ rat perfusion

Isabel Lozoya-Agullo, Moran Zur, Avital Beig, Noa Fine, Yael Cohen, Marta González-Álvarez, Matilde Merino-Sanjuán, Isabel González-Álvarez, Marival Bermejo, Arik Dahan

Research output: Contribution to journalArticlepeer-review

Abstract

Intestinal drug permeability is position dependent and pertains to a specific point along the intestinal membrane, and the resulted segmental-dependent permeability phenomenon has been recognized as a critical factor in the overall absorption of drug following oral administration. The aim of this research was to compare segmental-dependent permeability data obtained from two different rat intestinal perfusion approaches: the single-pass intestinal perfusion (SPIP) model and the closed-loop (Doluisio) rat perfusion method. The rat intestinal permeability of 12 model drugs with different permeability characteristics (low, moderate, and high, as well as passively and actively absorbed) was assessed in three small intestinal regions: the upper jejunum, mid-small intestine, and the terminal ileum, using both the SPIP and the Doluisio experimental methods. Excellent correlation was evident between the two approaches, especially in the upper jejunum (R2 = 0.95). Significant regional-dependent permeability was found in half of drugs studied, illustrating the importance and relevance of segmental-dependent intestinal permeability. Despite the differences between the two methods, highly comparable results were obtained by both methods, especially in the medium-high Peff range. In conclusion, the SPIP and the Doluisio method are both equally useful in obtaining crucial segmental-dependent intestinal permeability data.

Original languageAmerican English
Pages (from-to)201-208
Number of pages8
JournalInternational Journal of Pharmaceutics
Volume515
Issue number1-2
DOIs
StatePublished - 30 Dec 2016

Keywords

  • Biopharmaceutics classification system
  • Intestinal permeability
  • Oral drug absorption
  • Segmental-dependent permeability

All Science Journal Classification (ASJC) codes

  • Pharmaceutical Science

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