Administration of single doses of a drug are occasionally encountered in clinical practice, but it is more common to use single doses to determine the pharmacoki-
netic profile of a drug. Figures 5.1 and 5.2 illustrate such a use of single doses. Following a single dose, concentrations can be monitored until no longer analytically detectable and a complete pharmacokinetic profile is described.
In clinical practice, drugs are more commonly administered in multiple doses, with the second dose usually given before the first dose is completely eliminated. Figure 5.4 shows a representative time-concentration profile for multiple dosing of a drug with a t1/2 of 8 hours. With each successive dose up to approximately five doses, the concentration of drug keeps increasing, a phenomenon known as accumulation. The final concentrations of drug reached depend on the elimination rate of the drug, the dosing frequency, and the actual dose. Thus, for a given drug, concentrations will reach higher steady-state values if the drug is given more frequently or in greater doses. In contrast, the time to reach steady state is affected by neither the dose amount nor dosing frequency. The time to reach steady state is solely affected by the elimination rate (which is reflected in the t1/2). Giving a larger dose or giving the dose more often will not change the time needed to reach steady state (except in the case of a bolus dose, as discussed later).
Just as it takes approximately five half-lives for a drug to be essentially (97%) eliminated, it also requires five half-lives for a drug to reach steady state. This is exemplified in the concentration-time profiles of Figure 5.4. The hypothetical drug in this example has a half-life of 8 hours and is dosed every 8 hours. The graph shows that at about 40 hours (five half-lives), the maximum and minimum concentrations become consistent, indi-
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