PHAR 7632 Chapter 8

Pharmacokinetics of Oral Administration

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Integrated equation

We can also calculate the line (in Figure 8.2.3) using the integrated form of the equation can be derived using Laplace transforms.

If we use F • DOSE for Xg⁰ where F is the fraction of the dose absorbed, the integrated equation for Cp versus time is shown in Equation 8.3.1.

Equation 8.3.1 Drug Concentration after an Oral Dose

Notice that the right hand side of this equation (Equation 8.3.1) is a constant multiplied by the difference of two exponential terms. A biexponential equation.

We can plot Cp as a constant times the difference between two exponential curves (see Figure 2.2.1). If we plot each exponential separately.

Figure 8.3.1 Linear Plot of e^{-k' x t} versus Time for Two Exponential Terms

Notice that the difference starts at zero, increases, and finally decreases again toward a value of zero.

Plotting this difference multiplied by gives Cp versus time.

Figure 8.3.2 Linear Plot of Drug Concentration versus Time

We can calculate the plasma concentration at anytime if we know the values of all the parameters of Equation 8.3.1.

The parameters kel and V are dependent on the drug and the patient. Different patients will have different values for kel and V. This might depend on their age, weight, sex, genetic make-up (pharmacogenomics) and/or state of health. Different drugs can have quite different values of kel and V.

While dose is clearly a parameter associated with the dosage form, the parameters F and ka are partly determined by the drug and patient and also by the dosage form or route of administration. The rate (ka) and extent (F) of absorption can depend on the drug and patient with respect to transfer from the site of administration to the blood stream. The value of F may be reduced by poor solubility, drug instability, metabolism by intestinal flora, metabolism or reverse transport by various enzyme systems. The value of ka will be influenced by the drug dissolution rate and ability of the drug to move across any barriers between the site of administration and the blood stream. Both F and ka can also be influenced by the drug dosage form. Generally F is maximize but reduced values of ka may be desired to produce a sustained release effect.

Time of Peak Concentration

By setting the rate of change of Cp versus time, dCp/dt, to zero and after some rearranging an equation for the time of peak can be derived.

Equation 8.3.2 Time of Peak Concentration after an Oral Dose, t_peak or t_max

As an example we could calculate the peak plasma concentration given that F = 0.9, Dose = 600 mg, ka = 1.0 hr^-1, kel = 0.15 hr^-1, and V = 30 liter.

Using Equation 8.3.2

and now using Equation 8.3.1 we can calculate Cp_peak or Cp_max for a single oral dose

As another example we could consider what would happen with ka = 0.2 hr^-1 instead of 1.0 hr^-1

Using Equation 8.3.2

and now using Equation 8.3.1 we can calculate Cp_peak or Cp_max for a single oral dose

Note the peak drug concentration is lower and slower with the smaller ka value.

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ka
kel (Same Units as ka)

Time of Peak Cp is:
Dose
Bioavailability, F
Volume of Distribution

Peak Cp is: