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SKIN-CAD Overview > Features


New Features in Version 6.0
Addition of in vitro release data analysis
Addition of Freundlich-type binding scheme to skin permeation model
Addition of indirect response model to PK-PD model
Addition of automatic searching function of steady-state profile to in vitro skin permeation data analysis
Improvement of GUI
Improvement of deconvolution program for blood concentration data analysis
Addition of literature data to parameters list


Input Parameters
Patch application time, patch size
Device design (diffusion coefficient in matrix, drug loading, etc.)
Skin thickness, distance to blood vessels
Diffusion and partition coefficients in the skin
Systemic pharmacokinetic parameters.
Skin metabolism/binding parameters
Iontophoretic application parameters
Pharmacodynamic parameters, etc.


Parameters input window.

Output Data
Cumulative amount of drug permeated across the skin
Blood concentration - time profile
Distribution of drug concentration in the skin
Pharmacologic response - time profile


Graphical representation window.


New Features in Version 5.2
Addition of literature database: Diffusion Coefficient in Polymer
Addition of literature database: Skin Thickness of Human and Animals
Addition of literature database: Diffusion and Partition Coefficients in Skin of human and animals
Addition of literature database: Body Pharmacokinetic Parameters following intravenous administration in human

New Features in Version 5.1
Vehicle compartment model
Addition of simulation model: Vehicle Compartment + skin diffusion (2-layer or 1-layer) model ... this feature provides simple simulation in the case of "solution" donor phase (e.g. liquid formulation, in vitro permeation system...)
Dissolution-controlled model
Modification of simulation model: Dissolution-Controlled Model added to drug-dispersed matrix model ... in this model, dissolution-controlled scheme can be considered as well as diffusion-controlled step for drug release from matrix system
PK curve fitting
Modification of [Pharmacokinetics] curve-fitting function ... this feature provides curve-fitting functions for PK compartment models, which are available for Continuous Intravenous Infusion and Oral Administration as well as intravenous bolus injection
Deconvolution analysis
Addition of Deconvolution Method ... blood concentration data can be analyzed by deconvolution method together with i.v. bolus data, and fractional absorption can be estimated
Improved Features in Version 5.1
Improvement of graph drawing and printing

New Features in Version 5.0
Curve fitting function to compartment model
Curve fitting (non-linear regression analysis) function was added in order to calculate pharmacokinetic parameters. It is applicable to 1-, 2- and 3-comaprtment models from blood concentration data following intravenous administration.
Curve fitting function to Fick's second law
Curve fitting (non-linear regression analysis) function was added in order to calculate diffusion and partition coefficients in the skin. It is applicable to Fick's second law from drug distribution data in the stratum corneum obtained by tape-stripping technique.
Search function of in vitro steady-state permeation
Liniear regression program was added in order to determine the steady state for in vitro skin permeation profiles. This function makes it easy to search the steady-state profile, to evaluate permeation flux and time lag, and to calculate diffusion and partition parameters in the skin.
Improved Features in Version 5.0
Flexible settings of administration schedule (application period and system size) for multiple dose
Calculation of Tmax, Cmax and AUC for multiple administration

New features in Version 4.1
In version 4.1, diffusional release model of dispersed drug from matrix is added to skin permeation model.

New features in Version 4.0
In version 4.0, pharmacodynamic (PD) analysis is possible and pharmacokinetic (PK) analysis for total body is available for 1-, 2- and 3-compartmental model. User interface was also upgraded to be easy-to-use.





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