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

Authors :
Moran Zur
Matilde Merino-Sanjuán
Marival Bermejo
Isabel Lozoya-Agullo
Yael Cohen
Noa Fine
Isabel González-Álvarez
Avital Beig
Marta González-Álvarez
Arik Dahan
Source :
International Journal of Pharmaceutics. 515:201-208
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

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 ( R 2 = 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 P eff range. In conclusion, the SPIP and the Doluisio method are both equally useful in obtaining crucial segmental-dependent intestinal permeability data.

Details

ISSN :
03785173
Volume :
515
Database :
OpenAIRE
Journal :
International Journal of Pharmaceutics
Accession number :
edsair.doi.dedup.....0560449d05f7cee5fddc3fc3570dbcd2
Full Text :
https://doi.org/10.1016/j.ijpharm.2016.09.061