Medicines are available in various forms.
The tablet is the most common dosage form.
When a tablet is swallowed:
It first disintegrates in the stomach.
Dissolution occurs thereafter.
Dissolution defined:
Transition of drug molecules from a solid state (tablet particles) to a solution state (dissolved in gastric fluid).
Importance of gastric acidity:
The stomach’s highly acidic environment can lead to breakdown of some drug molecules.
After gastric processing:
Dissolved drug molecules are passed into the small intestine.
Here, drug molecules are absorbed across the epithelial layer.
Purpose of absorption:
Allows drugs to enter the bloodstream and circulate throughout the body to reach their target sites.
The efficiency of drug absorption is influenced by several key factors:
Dissolution: Rate at which the drug dissolves.
Solubility: Ability of the drug to dissolve in fluids.
Stability: Drug's ability to maintain its chemical integrity in the gastrointestinal environment.
Permeability: Ability of the drug to cross the intestinal barrier into the bloodstream.
These factors are determined by:
Physical properties of the tablet.
Chemical properties of the drug molecule.
Physiological factors related to the patient’s gastrointestinal system.
Grasping the drug absorption process is crucial:
Ensures efficacy of medicines administered via the oral route.