Literature DB >> 3772740

A diffusion-diffusion model for percutaneous drug absorption.

K Kubota, T Ishizaki.   

Abstract

Several theories describing percutaneous drug absorption have been proposed, incorporating the mathematical solutions of differential equations describing percutaneous drug absorption processes where the vehicle and skin are regarded as simple diffusion membranes. By a solution derived from Laplace transforms, the mean residence time MRT and the variance of the residence time VRT in the vehicle are expressed as simple elementary functions of the following five pharmacokinetic parameters characterizing the percutaneous drug absorption: kd, which is defined as the normalized diffusion coefficient of the skin, kc, which is defined as the normalized skin-capillary boundary clearance, the apparent length of diffusion of the skin 1d, the effective length of the vehicle lv, and the diffusion coefficient of the vehicle Dv. All five parameters can be obtained by the methods proposed here. Results of numerical computation indicate that: concentration-distance curves in the vehicle and skin approximate two curves which are simply expressed using trigonometric functions when sufficient time elapses after an ointment application; the most suitable condition for the assumption that the concentration of a drug in the uppermost epidermis can be considered unchanged is the case where the partition coefficient between vehicle and skin is small, and the constancy of drug concentration is even more valid when the effective length of the vehicle is large; and the amount of a drug in the vehicle or skin and the flow rate of the drug from vehicle into skin or from skin into blood becomes linear on a semilogarithmic scale, and the slopes of those lines are small when Dv is small, when the partition coefficient between vehicle and skin is small, when lv is large, or when kc is small. A simple simulation method is also proposed using a biexponential for the concentration-time curve for the skin near the skin-capillary boundary, that is, the flow rate-time curve for drug passing from skin into blood.

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Year:  1986        PMID: 3772740     DOI: 10.1007/bf01059200

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  18 in total

1.  Analysis of data on the medicament release from ointments.

Authors:  W I HIGUCHI
Journal:  J Pharm Sci       Date:  1962-08       Impact factor: 3.534

2.  Percutaneous absorption after twenty-five years: or "old wine in new wineskins".

Authors:  R J Scheuplein
Journal:  J Invest Dermatol       Date:  1976-07       Impact factor: 8.551

3.  Effect of topical vehicle composition on the in vitro release of fluocinolone acetonide and its acetate ester.

Authors:  B J Poulsen; E Young; V Coquilla; M Katz
Journal:  J Pharm Sci       Date:  1968-06       Impact factor: 3.534

4.  Percutaneous absorption of steroids.

Authors:  R J Scheuplein; I H Blank; G J Brauner; D J MacFarlane
Journal:  J Invest Dermatol       Date:  1969-01       Impact factor: 8.551

5.  A theoretical consideration of percutaneous drug absorption.

Authors:  K Kubota; T Ishizaki
Journal:  J Pharmacokinet Biopharm       Date:  1985-02

6.  Pharmacokinetics of transdermally delivered clonidine.

Authors:  T R MacGregor; K M Matzek; J J Keirns; R G van Wayjen; A van den Ende; R G van Tol
Journal:  Clin Pharmacol Ther       Date:  1985-09       Impact factor: 6.875

7.  Physicochemical interpretation of the pharmacokinetics of percutaneous absorption.

Authors:  R H Guy; J Hadgraft
Journal:  J Pharmacokinet Biopharm       Date:  1983-04

8.  Statistical moments in pharmacokinetics.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharmacokinet Biopharm       Date:  1978-12

9.  Pharmacokinetics and pharmacodynamics of transdermally administered clonidine.

Authors:  D Arndts; K Arndts
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

10.  Percutaneous absorption of flufenamic acid in rabbits: effect of dimethyl sulfoxide and various nonionic surface-active agents.

Authors:  C C Hwang; A G Danti
Journal:  J Pharm Sci       Date:  1983-08       Impact factor: 3.534

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  4 in total

1.  The relevance of residence time theory to pharmacokinetics.

Authors:  M Weiss
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

2.  Mathematical description of the uptake of hydrocarbons in jet fuel into the stratum corneum of human volunteers.

Authors:  David Kim; Matthew W Farthing; Cass T Miller; Leena A Nylander-French
Journal:  Toxicol Lett       Date:  2008-03-16       Impact factor: 4.372

3.  Analysis of drug penetration through the skin by the two-layer skin model.

Authors:  H Okamoto; F Yamashita; K Saito; M Hashida
Journal:  Pharm Res       Date:  1989-11       Impact factor: 4.200

4.  Quantification and statistical modeling--part II: dermal concentrations of monomeric and polymeric 1,6-hexamethylene diisocyanate.

Authors:  Kenneth W Fent; Linda G Trelles Gaines; Jennifer M Thomasen; Sheila L Flack; Kai Ding; Amy H Herring; Stephen G Whittaker; Leena A Nylander-French
Journal:  Ann Occup Hyg       Date:  2009-07-27
  4 in total

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