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Form, Pharmacokinetics, and Disposition Data

TABLE I. Dosage form, pharmacokinetics, and disposition data... [Pg.447]

Even though the absorption rate constant (kf) defines the rate of absorption, its accurate determination is largely dependent on the adequacy of the plasma concentration-time data associated with the absorption phase of the drug. When a drug is administered orally, as a conventional (immediate-release) dosage form, or injected intramuscularly as an aqueous parenteral solution, the absorption and disposition kinetics can often be analysed in terms of a one-compartment pharmacokinetic model with apparent first-order absorption. The plasma concentration-time curve is described by the equation... [Pg.56]


See other pages where Form, Pharmacokinetics, and Disposition Data is mentioned: [Pg.446]    [Pg.446]    [Pg.2155]    [Pg.32]    [Pg.234]    [Pg.258]    [Pg.858]    [Pg.239]    [Pg.858]    [Pg.667]    [Pg.20]    [Pg.216]    [Pg.81]    [Pg.2064]    [Pg.57]    [Pg.361]   


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Pharmacokinetic Data

Pharmacokinetics disposition

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