Diffusion modeling of percutaneous absorption kinetics: 3. Variable diffusion and partition coefficients, consequences for stratum corneum depth profiles and desorption kinetics.

Stratum corneum (SC) desorption experiments have yielded higher calculated steady-state fluxes than those obtained by epidermal penetration studies. A possible explanation of this result is a variable diffusion or partition coefficient across the SC. We therefore developed the diffusion model for percutaneous penetration and desorption to study the effects of either a variable diffusion coefficient or variable partition coefficient in the SC over the diffusion path length. Steady-state flux, lag time, and mean desorption time were obtained from Laplace domain solutions. Numerical inversion of the Laplace domain solutions was used for simulations of solute concentration-distance and amount penetrated (desorbed)-time profiles. Diffusion and partition coefficients heterogeneity were examined using six different models. The effect of heterogeneity on predicted flux from desorption studies was compared with that obtained in permeation studies. Partition coefficient heterogeneity had a more profound effect on predicted fluxes than diffusion coefficient heterogeneity. Concentration-distance profiles show even larger dependence on heterogeneity, which is consistent with experimental tape-stripping data reported for clobetasol propionate and other solutes. The clobetasol propionate tape-stripping data were most consistent with the partition coefficient decreasing exponentially for half the SC and then becoming a constant for the remaining SC.

[1]  J. Hadgraft,et al.  PHYSICOCHEMICAL DETERMINANTS OF STRATUM CORNEUM PERMEATION , 1998 .

[2]  G. Menon,et al.  Mode of action of glycolic acid on human stratum corneum: ultrastructural and functional evaluation of the epidermal barrier , 1997, Archives of Dermatological Research.

[3]  I. Brody A light and electron microscopy study of normal human stratum corneum with particular reference to the intercellular space. , 1989, Upsala journal of medical sciences.

[4]  Y. Lo,et al.  Noninvasive Characterization of Regional Variation in Drug Transport into Human Stratum Corneum in Vivo , 2003, Pharmaceutical Research.

[5]  R. Guy,et al.  The determination of a diffusional pathlength through the stratum corneum. , 1999, International journal of pharmaceutics.

[6]  M. Roberts,et al.  Permeability of solutes through biological membranes measured by a desorption technique , 1975, Nature.

[7]  R. Scheuplein,et al.  “Bound Water” in Keratin Membranes measured by a Microbalance Technique , 1967, Nature.

[8]  Y. Kalia,et al.  Characterization of the permeability barrier of human skin in vivo. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[9]  R. Siegel Algebraic, differential, and integral relations for membranes in series and other multilaminar media: Permeabilities, solute consumption, lag times, and mean first passage times , 1991 .

[10]  M. Roberts,et al.  Water. The most natural penetration enhancer , 1993 .

[11]  P A Bowser,et al.  Isolation, barrier properties and lipid analysis of stratum compactum, a discrete region of the stratum corneum , 1985, The British journal of dermatology.

[12]  Roberts,et al.  Diffusion modeling of percutaneous absorption kinetics. 1. Effects of flow rate, receptor sampling rate, and viable epidermal resistance for a constant donor concentration. , 2000, Journal of pharmaceutical sciences.

[13]  R. Scheuplein,et al.  Permeability of the Skin , 1971 .

[14]  R H Guy,et al.  Homogeneous transport in a heterogeneous membrane: water diffusion across human stratum corneum in vivo. , 1996, Biophysical journal.

[15]  John Crank,et al.  The Mathematics Of Diffusion , 1956 .

[16]  A. Naik,et al.  Computer simulation of penetrant concentration-depth profiles in the stratum corneum , 1992 .

[17]  M. Roberts,et al.  Diffusion modeling of percutaneous absorption kinetics: 2. Finite vehicle volume and solvent deposited solids. , 2001, Journal of pharmaceutical sciences.

[18]  R. Purves Accuracy of numerical inversion of Laplace transforms for pharmacokinetic parameter estimation. , 1995, Journal of Pharmacy and Science.