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After six hours the plasma concentration will fall to 2 mg/liter. If we give the same dose again the plasma concentration will increase by 4 mg/liter from 2 mg/liter to 6 mg/liter. Then after another half-life (6 hours) the plasma concentration will fall to 3 mg/liter. Again, another dose will increase the plasma concentration by 4 mg/liter to 7 mg/liter. After another half-life the plasma concentration will be 3.5 mg/liter. After repeated drug administration every six hours the plasma concentration will accumulate until it fluctuates between a maximum and minimum value of 8 mg/liter and 4 mg/liter. In this example the dose was given every drug elimination half-life of 6 hours. Note, the amount of drug eliminated or the drug concentration drop during one half-life increases as the concentration increases. Remember elimination is considered to be a first order process!
Figure 14.4.1 Linear Plot of Cp versus Time Showing Doses Every Six Hours
Click on the figure to view the interactive graph
With each dose, drug accumulated until the amount of drug eliminated during each dosing interval was equal to the amount of the dose. In the first interval plasma concentrations fall from 4 to 2 mg/L. Continuing for a number of doses gives the following table.
Dose Number | Start | End | Concentration lost during dosage interval | |
1 | 4 | --> | 2 mg/L | 2 mg/L |
2 | 6 | --> | 3 | 3 |
3 | 7 | --> | 3.5 | 3.5 |
4 | 7.5 | --> | 3.75 | 3.75 |
... | ... | |||
n = ∞ | 8 | --> | 4 | 4 <- which is the same as the concentration increase caused by each dose |
There is a limit to drug accumulation because as the plasma concentration increased the amount of drug eliminated during the dosing interval will also increase as the rate of elimination is equal to the amount of the drug in the body multiplied by the rate constant for a first order elimination. (Compare this with the case of a continuous infusion).
So far we can see that if we give repeated doses before the body can eliminate the previous doses then we will get accumulation of the drug. We have also seen that when we have first order elimination this accumulation will not proceed indefinitely but will approach a steady state.
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