Accessibility navigation


Drug permeability in 16HBE14o- airway cell layers correlates with absorption from the isolated perfused rat lung

Manford, F., Tronde, A., Jeppsson, A.-B., Patel, N. ORCID: https://orcid.org/0000-0002-8600-0663, Johansson, F. and Forbes, B. (2005) Drug permeability in 16HBE14o- airway cell layers correlates with absorption from the isolated perfused rat lung. European Journal of Pharmaceutical Sciences, 26 (5). pp. 414-20. ISSN 0928-0987

Full text not archived in this repository.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item DOI: 10.1016/j.ejps.2005.07.010

Abstract/Summary

The permeability of the lung is critical in determining the disposition of inhaled drugs and the respiratory epithelium provides the main physical barrier to drug absorption. The 16HBE14o- human bronchial epithelial cell line has been developed recently as a model of the airway epithelium. In this study, the transport of 10 low molecular weight compounds was measured in the 16HBE14o- cell layers, with apical to basolateral (absorptive) apparent permeability coefficients (P(app)) ranging from 0.4 x 10(-6)cms(-1) for Tyr-D-Arg-Phe-Phe-NH(2) to 25.2x10(-6)cms(-1) for metoprolol. Permeability in 16HBE14o- cells was found to correlate with previously reported P(app) in Caco-2 cells and absorption rates in the isolated perfused rat lung (k(a,lung)) and the rat lung in vivo (k(a,in vivo)). Log linear relationships were established between P(app) in 16HBE14o- cells and P(app) in Caco-2 cells (r(2)=0.82), k(a,lung) (r(2)=0.78) and k(a,in vivo) (r(2)=0.68). The findings suggest that permeability in 16HBE14o- cells may be useful to predict the permeability of compounds in the lung, although no advantage of using the organ-specific cell line 16HBE14o- compared to Caco-2 cells was found in this study.

Item Type:Article
Refereed:Yes
Divisions:No Reading authors. Back catalogue items
ID Code:37505
Uncontrolled Keywords:16HBE14o-; Epithelium; Caco-2; Pulmonary absorption; In vitro–in vivo correlation; Rat
Publisher:Elsevier

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation