A comparative ex vivo drug permeation study of beta-blockers through porcine buccal mucosa

Int J Pharm. 2014 Jul 1;468(1-2):50-4. doi: 10.1016/j.ijpharm.2014.03.050. Epub 2014 Apr 13.

Abstract

Apparent permeability coefficients (kp) of a series of beta-blockers: acebutolol, atenolol, labetalol, metoprolol, oxprenolol and propranolol, through porcine buccal mucosa were determined. The aim of the study was to determine the permeation parameters (apparent permeability coefficient, kp; flux, J; and lag time, TL) as a measure of the intrinsic permeability of porcine buccal mucosa to these drugs, in order to predict the efficacy of their possible administration through human buccal mucosa. A positive linear correlation was observed between the apparent permeability coefficient, kpand the partition coefficient, P. Oxprenolol and propranolol are the drugs that presented the highest values of kp: 0.3231×10(2) cm/h and 0.5666×10(2) cm/h, respectively. Multiple linear regression (MLR) using least square estimation was performed on the data set with logkpas dependent variable and the descriptors as predictor variables. The potential systemic capacity after a buccal administration was predicted by estimating the plasma concentrations at steady-stated (Css). Considering the entire process of permeation ex vivo, propranolol and oxprenolol would seem to be the best candidates for administration through the buccal mucosa.

Keywords: Beta-blockers; Buccal permeation; Ex vivo drug permeation; Porcine buccal mucosa.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Buccal
  • Adrenergic beta-Antagonists / administration & dosage
  • Adrenergic beta-Antagonists / chemistry
  • Adrenergic beta-Antagonists / metabolism*
  • Animals
  • Biological Transport
  • Humans
  • In Vitro Techniques
  • Least-Squares Analysis
  • Linear Models
  • Models, Biological
  • Molecular Structure
  • Mouth Mucosa / metabolism*
  • Oxprenolol / metabolism
  • Permeability
  • Propranolol / metabolism
  • Structure-Activity Relationship
  • Swine

Substances

  • Adrenergic beta-Antagonists
  • Oxprenolol
  • Propranolol