![]() |
|
|
Vol. 280, Issue 2, 747-753, 1997
ich
Kope
ek1
Department of Pharmaceutics and Pharmaceutical Chemistry/CCCD,
University of Utah, Salt Lake City, Utah
Colon-specific delivery of metabolically labile molecules, such as
proteins and peptides, is of particular interest in pharmaceutical research. Among the factors that may influence the permeability of drug
molecules across colonic mucosa are their molecular weight and
geometry. The purpose of this study was to evaluate the influence of
molecular geometry on in vitro permeability across rabbit
distal colonic epithelia. Permeability of radiolabeled hydrophilic
probes with different molecular weights and geometries across isolated rabbit distal colonic tissue was evaluated by means of the Ussing chamber technique. The hydrodynamic radii of the probes (an indicator of molecular geometry) were estimated by theoretical models as well as
dynamic light scattering. We conducted the permeability studies in the
presence and absence of the epithelial cells to evaluate the
contribution of the underlying connective tissue to the overall
in vitro permeability across the colonic mucosa. The rank
order of the permeability of the markers was mannitol > lactulose > polyethylene glycol (PEG) 400 > PEG 900 > PEG 4000, which is consistent with their molecular weights and
estimated hydrodynamic radii. The permeability of inulin, a
polyfructose molecule with a molecular weight of about 5000, however,
was approximately the same as that of PEG 900 (molecular weight about
900). When the epithelial cells were removed, for the homologous series
of PEGs, the permeabilities were proportional to their free diffusion coefficients in water. It appears that for the PEG and lactulose probes, theoretical estimation of the hydrodynamic radii, which assumes
the molecules to be spherical in shape, provides a good basis for the
dependence of permeability on geometry. The relatively high
permeability of inulin seems to be due to its compact structure. The
PEG permeability values in the absence of epithelial cells, in
combination with their diffusion coefficients, indicate that the
underlying connective tissue does not contribute to the overall permeability of these molecules across colonic mucosa in
vitro.
This article has been cited by other articles:
![]() |
C. M. Van Itallie, J. Holmes, A. Bridges, J. L. Gookin, M. R. Coccaro, W. Proctor, O. R. Colegio, and J. M. Anderson The density of small tight junction pores varies among cell types and is increased by expression of claudin-2 J. Cell Sci., February 1, 2008; 121(3): 298 - 305. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. R. Tracy, T. J. McWhorter, C. Korine, M. S. Wojciechowski, B. Pinshow, and W. H. Karasov Absorption of sugars in the Egyptian fruit bat (Rousettus aegyptiacus): a paradox explained J. Exp. Biol., May 15, 2007; 210(10): 1726 - 1734. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. El-Sayed, M. Ginski, C. A. Rhodes, and H. Ghandehari Influence of Surface Chemistry of Poly(Amidoamine) Dendrimers on Caco-2 Cell Monolayers Journal of Bioactive and Compatible Polymers, January 1, 2003; 18(1): 7 - 22. [Abstract] [PDF] |
||||
![]() |
T. Lindmark, Y. Kimura, and P. Artursson Absorption Enhancement through Intracellular Regulation of Tight Junction Permeability by Medium Chain Fatty Acids in Caco-2 Cells J. Pharmacol. Exp. Ther., January 1, 1998; 284(1): 362 - 369. [Abstract] [Full Text] |
||||