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Multiple dosing pharmacokinetic models absorption

These linear kinetic models and diffusion models of skin absorption kinetics have a number of features in common they are subject to similar constraints and have a similar theoretical basis. The kinetic models, however, are more versatile and are potentially powerful predictive tools used to simulate various aspects of percutaneous absorption. Techniques for simulating multiple-dose behavior evaporation, cutaneous metabolism, microbial degradation, and other surface-loss processes dermal risk assessment transdermal drug delivery and vehicle effects have all been described. Recently, more sophisticated approaches involving physiologically relevant perfusion-limited models for simulating skin absorption pharmacokinetics have been described. These advanced models provide the conceptual framework from which experiments may be designed to simultaneously assess the role of the cutaneous vasculature and cutaneous metabolism in percutaneous absorption. [Pg.2423]


See other pages where Multiple dosing pharmacokinetic models absorption is mentioned: [Pg.2494]    [Pg.351]    [Pg.767]    [Pg.267]    [Pg.145]    [Pg.359]    [Pg.768]   
See also in sourсe #XX -- [ Pg.266 , Pg.267 , Pg.268 , Pg.269 , Pg.270 ]




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