2. The study of the disposition of a drug
The disposition of a drug includes the processes of ADME
Absorption
Distribution
Metabolism
Excretion
Drug concentration at sites of action influenced by several
factors, such as:
◦ Route of administration
◦ Dose
◦ Characteristics of drug molecules (e.g., lipid solubility)
3.
4. 3 main – bioavailability of drug
Cmax: point of max conc. In plasma.
◦ Expressed in mcg/ml
◦ Dependent on
Dose administered
Rate of absorption
Rate of elemination
Tmax: time taken to attain Cmax
Expressed in hrs
Onset of action is depended on tmax
AUC: total integrated area under plasma level-time and
expresses the amount of drug that reaches the systemic
circulation
7. The process by which drug proceeds from the site of
administration to the site of measurement (blood stream)
within the body.
Necessary for the production of a therapeutic effect.
Most drugs undergo gastrointestinal absorption. This is extent
to which drug is absorbed from gut lumen into portal
circulation
Exception: IV drug administration
8.
9.
10.
11.
12. The movement of drug from the blood
to and from the tissues
Determined by:
• partitioning across various membranes
•binding to tissue components
•binding to blood components (RBC, plasma protein)
•physiological volumes