Izvorni znanstveni članak

https://doi.org/10.2478/v10007-009-0038-3

Permeation of losartan across human respiratory epithelium: An in vitro study with Calu-3 cells

MICHELLE AMOAKO-TUFFOUR ; Biopharmaceutics and Drug Delivery Laboratory, College of Pharmacy, Faculty of Health Professions, Dalhousie University, Halifax, NS, Canada B3H 3J5
POLLEN K. YEUNG ; Pharmacokinetics and Metabolism Laboratory, College of Pharmacy, Faculty of Health Professions, Dalhousie University, Halifax, NS, Canada B3H 3J5
REMIGIUS U. AGU AGU orcid.org/0000-0001-6091-1840 ; Biopharmaceutics and Drug Delivery Laboratory, College of Pharmacy, Faculty of Health Professions, Dalhousie University, Halifax, NS, Canada B3H 3J5

Sažetak

The potential for nasal delivery of losartan, a drug with poor oral bioavailability, was investigated using Calu-3 cells. Epithelial permeation of the drug with or without dimethyl-β-cyclodextrin (DM--CD) and glycocholate was investigated. Possible transport mechanism of the compound and epithelial mucosal tolerance were screened. Reversibility of epithelial membrane perturbation was also investigated by measuring transepithelial electrical resistance (TEER) recovery over a 24-h period following drug formulation exposure. The permeability coefficient of losartan was 1.3 ± 0.5 × 10-6 cm s-1. This flux was not significantly different from that of formulations containing DM--CD (0.5 and 1.0 %) or glycocholate (0.5 %). However, the formulation with 1.0 % glycocholate significantly increased losartan permeation 7-fold. Losartan flux across the cells was concentration-dependent. Serosal to mucosal permeation was significantly higher than mucosal to serosal permeation. Concentration-dependency, as well as polarity in transport indicated that the flux of the compound across Calu-3 cells was not limited to passive diffusion. Cells exposed to DM--CD (0.5 and 1.0 %) and glycocholate (0.5 %) caused no significant change in TEER and mitochondrial dehydrogenase activity (MDH). The results of the study showed that losartan may be a suitable drug candidate for nasal delivery.

Ključne riječi

permeation; losartan; nasal absorption; Calu-3 cells

Hrčak ID:

40739

URI

https://hrcak.srce.hr/40739

Datum izdavanja:

1.12.2009.

Podaci na drugim jezicima: hrvatski

Posjeta: 1.952 *