A loading dose is most useful for drugs that are eliminated from the body relatively slowly, i.e. have a long systemic half-life. Such drugs need only a low maintenance dose in order to keep the amount of the drug in the body at the appropriate therapeutic level, but this also means that, without an initial higher dose, it would take a long time for the amount of the drug in the body to reach that level.
For an example, one might consider the hypothetical drug foosporin. Suppose it has a long lifetime in the body, and only ten percent of it is cleared from the blood each day by the liver and kidneys. Suppose also that the drug works best when the total amount in the body is exactly one gram. So, the maintenance dose of foosporin is 100 milligrams (100 mg) per day—just enough to offset the amount cleared.
Suppose a patient just started taking 100 mg of foosporin every day.
- On the first day, they'd have 100 mg in their system; their body would clear 10 mg, leaving 90 mg.
- On the second day, the patient would have 190 mg in total; their body would clear 19 mg, leaving 171 mg.
- On the third day, they'd be up to 271 mg total; their body would clear 27 mg, leaving 244 mg.
As one can see, it would take many days for the total amount of drug within the body to come close to 1 gram (1000 mg) and achieve its full therapeutic effect.
For a drug such as this, a doctor might prescribe a loading dose of one gram to be taken on the first day. That immediately gets the drug's concentration in the body up to the therapeutically-useful level.
- First day: 1000 mg; the body clears 100 mg, leaving 900 mg.
- On the second day, the patient takes 100 mg, bringing the level back to 1000 mg; the body clears 100 mg overnight, still leaving 900 mg, and so forth.
Calculating the loading dose
Four variables are used to calculate the loading dose:
Cp = desired peak concentration of drug Vd = volume of distribution of drug in body F = bioavailability S = fraction of drug salt form which is active drug
The required loading dose may then be calculated as
For an intravenously administered drug, the bioavailability F will equal 1, since the drug is directly introduced to the bloodstream. If the patient requires an oral dose, bioavailability will be less than 1 (depending upon absorption, first pass metabolism etc.), requiring a larger loading dose.
Sample values and equations
|Dose||Amount of drug administered.||500 mg||Design parameter|
|Dosing interval||Time between drug dose administrations.||24 h||Design parameter|
|Cmax||The peak plasma concentration of a drug after administration.||60.9 mg/L||Direct measurement|
|tmax||Time to reach Cmax.||3.9 h||Direct measurement|
|Cmin||The lowest (trough) concentration that a drug reaches before the next dose is administered.||27.7 mg/L||Direct measurement|
|Volume of distribution||The apparent volume in which a drug is distributed (i.e., the parameter relating drug concentration in plasma to drug amount in the body).||6.0 L|
|Concentration||Amount of drug in a given volume of plasma.||83.3 mg/L|
|Elimination half-life||The time required for the concentration of the drug to reach half of its original value.||12 h|
|Elimination rate constant||The rate at which a drug is removed from the body.||0.0578 h−1|
|Infusion rate||Rate of infusion required to balance elimination.||50 mg/h|
|Area under the curve||The integral of the concentration-time curve (after a single dose or in steady state).||1,320 mg/L·h|
|Clearance||The volume of plasma cleared of the drug per unit time.||0.38 L/h|
|Bioavailability||The systemically available fraction of a drug.||0.8|
|Fluctuation||Peak trough fluctuation within one dosing interval at steady state.||41.8 %||