p.1
Drug Absorption Mechanisms
What type of drugs are absorbed in the stomach?
Non-ionized, non-polar, lipid-soluble drugs.
p.1
Controlled Medication Dynamics
What factors affect sustained release of medications?
Interaction with body fluid, Medium pH, Enzymatic activity.
p.1
Volume of Distribution Factors
How does obesity affect lipid-soluble drugs?
It increases the volume of distribution.
What characterizes first-order kinetics?
<p>Rate is directly proportional to the concentration (linear)</p>
p.1
Blood-Brain Barrier Penetration
What characteristics allow drugs to cross the Blood-Brain Barrier?
Unionized and lipophilic properties.
p.1
Volume of Distribution Factors
What is the effect of volume of distribution?
It is influenced by solubility, protein binding, and molecular weight.
What is a key feature of zero-order kinetics?
<p>Rate is independent of the concentration (non-linear).</p>
p.1
Drug Distribution Compartments
What is the excretion pathway for drugs with molecular weight > 500?
They will be excreted in the biliary system.
Which medications are examples of zero-order kinetics?
Warfarin, Alcohol, Aspirin, Theophylline, Tolbutamide, Phenytoin.
p.1
Placental Drug Transfer
What factors allow drugs to cross the placenta?
Molecular weight < 500, lipophilic, and non-ionized.