# Loading dose

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Loading dose

A loading dose is an initial higher dose of a drug that may be given at the beginning of a course of treatment before dropping down to a lower maintenance dose.[1]

A loading dose is most useful for drugs that are eliminated from the body relatively slowly. Such drugs need only a low maintenance dose in order to keep the amount of the drug in the body at the appropriate 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.

Drugs which may be started with an initial loading dose include digoxin, teicoplanin, voriconazole and procainamide. Phenytoin for acute status epilepticus should also be given with an initial loading dose, co-administered with a benzodiazepine, to immediately stabilize neuronal membranes and electrical activity during a seizure.

## Worked example

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 = salt fraction

The required loading dose may then be calculated as

$\mbox{Loading dose} = \frac{C_p V_d}{F S}$

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

Characteristic Description Example value Abbreviation(s) Formula
Dose Loading dose (LD), or steady state / maintenance dose (MD). 500 mg $\textstyle D$ design parameter
τ Dosing interval. 24 h $\textstyle \tau$ design parameter
Volume of distribution The apparent volume in which a drug is distributed immediately after it has been injected intravenously and equilibrated between plasma and the surrounding tissues. 6.0 L $\textstyle V_d$ $\textstyle = D / C_0$
Concentration Initial or steady-state concentration of drug in plasma. 83.3 µg/mL $\textstyle C_{0} \ or \ C_{ss}$ $\textstyle = D / V_d$
Biological half-life The time required for the concentration of the drug to reach half of its original value. 12 h $\textstyle t_{1/2}$ $\textstyle = ln (2) / k_{e}$
Elimination rate constant The rate at which drugs are removed from the body. 0.0578 h-1 $\textstyle k_e$ $\textstyle = ln (2) / t_{1/2} = CL / V_{d}$
Elimination rate Rate of infusion required to balance elimination. 50 mg/h $\textstyle k_{in}$ $\textstyle = C_{ss} \cdot CL$
Area under the curve The integral of the concentration-time curve (after a single dose or in steady state). 1320 µg/mL×h $\textstyle AUC_{0-\infty}$

$\textstyle AUC_{\tau,ss}$
$= \int_{0}^{\infty}C\, dt$
$= \int_{t}^{t+\tau}C\, dt$
Clearance The volume of plasma cleared of the drug per unit time. 0.38 L/h $\textstyle CL$ $\textstyle= V_{d} \cdot k_{e} = D/AUC$
Bioavailability The fraction of drug that is absorbed. 0.8 $\textstyle f$ $= \frac{AUC_{po}\cdot D_{iv}}{AUC_{iv}\cdot D_{po}}$
Cmax The peak plasma concentration of a drug after oral administration. 60.9 µg/mL $\textstyle C_{max}$ direct measurement
tmax Time to reach Cmax. 3.9 h $\textstyle t_{max}$ direct measurement
Cmin The lowest (trough) concentration that a drug reaches before the next dose is administered. 27.7 µg/mL $\textstyle C_{min,ss}$ direct measurement
Fluctuation Peak trough fluctuation within one dosing interval at steady state 41.8 % $\textstyle %PTF$ $\textstyle =100 \cdot \frac{(C_{max,ss} - C_{min,ss})}{C_{av,ss}}$
where
$\textstyle C_{av,ss}=\frac{AUC_{\tau,ss}}{\tau}$
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## References

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