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These flashcards cover essential vocabulary related to pharmacokinetics, including processes of drug absorption, ionization, and the impact of pKa and pH on drug effectiveness.
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Pharmacokinetics
Quantitative study of drug movement through the body
Absorption
The transfer of a drug from its site of administration to the bloodstream.
Passive diffusion
A process where drug molecules move across a membrane down their concentration gradient without using energy.
Active transport
Movement of drug molecules across a membrane against their concentration gradient, requiring energy (ATP).
pKa
The pH at which 50% of a drug is ionized and 50% is unionized.
Ionization
The process by which a drug molecule gains or loses an electrical charge, affecting its ability to cross cell membranes.
Bioavailability
The degree and rate at which a drug or active ingredient is absorbed and becomes available at the site of action.
Henderson-Hasselbalch equation
A mathematical formula used to calculate the pH of a solution based on the concentration ratio of protonated and unprotonated forms of a weak acid or base.
Weak acid
A type of acid that only partially ionizes in solution.
Weak base
A type of base that only partially ionizes in solution.
AUC (Area Under the Curve)
A measure of the total exposure of the body to a drug over time.
Volume of distribution (Vd)
A calculated value that helps to understand how a drug is distributed in the body.
Plasma protein binding
The degree to which drugs attach to proteins in the blood, affecting their distribution and effects.
Lipid-soluble drugs
Drugs that can easily pass through cell membranes due to their ability to dissolve in lipids.
Water-soluble drugs
Drugs that have an electrical charge and generally cannot cross cell membranes easily.
pH
A measure of the acidity or basicity of a solution, significantly influencing drug ionization.
Acidic drug
A drug that releases protons (H+) in solution, tending to remain non-ionized in acidic environments.
Basic drug
A drug that accepts protons (H+) in solution, tending to remain non-ionized in basic environments.
in order to reach their site of action
a drug has to pass through several membranes
transport against concentration gradient
active transport