Canonical Question
PK – Half-life
Master answer
Definitions
Half life: Time taken for a reduction in one half the total ammount of drug from the body.
Half time: Time taken for a reduction in one half the plasma concentration of a drug

Simplified equation for half life
\[T_{1/2} = {{\ln(2)\; \times\; Vd} \over {Cl}}\]
- Where
- Vd is volume of distribution of a drug
- Cl is its clearance
- ln(2), the natural log of 2, can be approximated as 0.693
Pharmacokinetic factors
Absorption
- Minimal impact on T1/2
- If initial plasma concentration saturates its metabolic pathway, clearance will become zero-order and rate of elimination will be independent of drug concentration
Distribution
- In the multi-compartment pharmacokinetic model,
- Drug initially entering the central (plasma) compartment will redistribute to other compartments (tissues), decreasing the amount remaining in the central compartment.
- As Vd increases, the ammount redistributing to other tissues increases → increased distribution away from central compartment → T1/2α (Distribution half time) decreases.
- This reduction in plasma concentration will decrease the concentration of drug reaching its metabolic organs (unless plasma metabolism) and prolong the elimination half-life.
- Drugs with high volumes of distribution display context-sensitive half time
- Protein binding of drug increases half life
- Prevents glomerular filtration

Metabolism and elimination
- Clearance is the volume of plasma completely cleared of drug per unit time
- Total body clearance is a sum of renal clearance (via metabolism or elimination), hepatic clearance (via metabolism, biliary secretion) and other mechanisms (such as lung metabolism, plasma cholinesterases etc.)
- As drug metabolism and elimination increases, T1/2β decreases
Zero-order kinetics
- As elimination of drug is independent of drug concentration, half life is not constant and progressively shorten by half
- E.g. 100mg of drug in body eliminated at 10mg/hr hour
- Half life from 100mg (to 50mg) would be 5 hours
- Subsequent half life (from 50mg to 25mg) would be 2.5 hours etc.
- E.g. 100mg of drug in body eliminated at 10mg/hr hour
Sakurai 2016
Exam appearances
| Exam | Exact wording | Relationship | Success |
|---|---|---|---|
| 2012B Q11 | Discuss the pharmacokinetic factors that affect drug half-life. | historical_member | — |