Volume of distribution after oral or IM administration
V = amount of drug administered/KxAUC
Peak plasma concentration following an oral dose occurs when
elimination = absorption
Short time to peak =
rapid absorption
Absorption rate
fraction of drug present at the absorption site that is absorbed per unit time
if Ka is greater than 1
in a time unit almost all drug would be absorbed over that time
High Ka indicates
rapid absorption
Ka equals
the negative slope of the residual line
MEC
minimal effective concentration
Onset is where
drug concentration levels reach the MEC
Offset is where
drug plasma levels fall below MEC
tmax is when
time of peak plasma concentration
MTC
Minimal toxic concentration
Ks
rate describing disintegration and dissolution of a solid dosage form
Proceses which control the rate of drug going into solution also control
the rate of absorption
generally Ks is _____ than Ka
much smaller
products which contain essentially identical amounts of the identical active ingredient in identical dosage forms, and which meet existing physicochemical standards
chemical equivalents
chemical equivalents which when administered in the same amounts will provide essentially the same bioavailability, as measured by blood levels or urinary excretions
biological equivalents
chemical equivalents which when administered in the same amounts will provide essentially the same therapeutic effect as measured by the control of a symptom or a disease
therapeutic equivalents
the ultimate criterion for assessing equivalence of drug products
therapeutic equivalents
F =
absolute bioavailability from the oral dosage form or the fraction of the dose which actually reaches the systemic circulation
Greatest factor which can affect the extent to which a number of drugs are absorbed