DR ZAREEN NAZ Assistant Professor Pharmacology Routes of drug administration
• Enteral (Through Alimentary tract)
• Parenteral (Through Injection) Factors affecting drug absorption • 1-Lipid-water partition co-efficient: Non electrolyte drug depends upon lipid solubility. • More lipid soluble and less water soluble that is has high lipid-water partition co-efficient, it will absorbed rapidly • 2- Drug solubility: drugs given in aqueous solutions are more rapidly soluble than when given in oily solution, suspension or solid form.
• 3- Dosage form: Tablets and capsules, rate of
disintegration and dissolution is limiting factor in their absorption. After dissolution, smaller the particle size, more efficient will be absorption. • 4- Circulation at the site: Increased blood flow increase absorption • How blood flow increase? • How blood flow decrease?
• 5- Area of absorbing surface : Absorbed
more from large surface areas for example intestinal mucosa • 6- Effect of pH: • Most drugs are either weak acids or weak bases. Weak electrolytes, in addition to lipid solubility, depends upon its degree of ionization which is influenced by pH of the area. • Weak acids become less ionized(charged) in an acidic medium and weak bases become less ionized in an alkaline medium • Unionized drug is lipid soluble and diffusible • Acidic drug will absorb more in stomach or intestine?
• Basic drug will absorb more from intestine
because it becomes unionized in basic medium. • In acidic medium basic drug will become more ionized and thus no absorption will takes place. • 7. Functional integrity of the GIT: • Increased peristaltic activity as in diarrhea reduces drug absorption • Increased gastric emptying time, absorption will be more. Bioavailability • The fraction of unchanged drug reaching the systemic circulation following administration by any route” or
The percentage of administered drug that reaches
the systemic circulation in a chemically unchanged form” • Thus by definition a drug that is administered by intravenous route has 100% bioavailability