Movement of drug form site of administration to the central compartment (blood)
Absorption
Rate & Extent of disappearance of a drug from the site of administration
Physiologic
Rate & extent of drug entry into systemic circulation
Pharmacokinetic
Factors Affecting Absorption
Dose Size
⬆️dose = ⬆️absorption
Absorption Environment
* Small Intestine
Surface Area of the Absorption Environment
⬆️Surface Area = ⬆️Absorption
Main site of drug absorption
Small Intestine
– SA = 120 m2 (villi& microvilli)
pH of the Absorption Environment
* SI — Basic (⬆️pH)
Weak Acid
* SI: ionized (excreted)
Weak Base
* SI: Non-ionized (absorbed)
Degree of Perfusion — Blood Supply
⬆️Perfusion = ⬆️Absorption
– For PO drugs
– Time it takes for the stomach to empty its contents
Gastric Emptying Time (GET)
Stomach
– Small Surface Area
– Small perfusion
— POOR ABSORPTION Environment except ASA & Ethanol
Gastric Emptying Time (GET)
⬆️GET = ⬇️Absorption
Normal Gastric Emptying Time
2-3 hours
Factors that ⬆️ GET
Factors that ⬇️ GET
Pharmacokinetic Parameters
* Bioequivalence
Measurement of RATE AND EXTENT of drug absorption
Bioavailability
Methods
* Plasma Concentration vs Time Graph
Parameters
– Maximum drug plasma concentration
– Measure BOTH rate and extent
– Most variable
Cmax
– Time to reach Cmax
– Measures the RATE
Tmax