General principles of Pharmacology Flashcards
General principles of pharmacology are:
(1) The factors that affect the actions of drugs.
(2) Factors that affect drug reactions.
(3) Various types of drug interactions.
(4) Factors influencing drug response interactions.
Pharmacokinetic: Activities of the drug after it enters the body. Pharmacokinetics is the study of drug absorption, distribution, metabolism, and excretion.
A fundamental concept in pharmacokinetics is drug clearance, that is, elimination of drugs from the body.
Absorption: The transfer of the drug from the body fluids to the tissues.
(1) Active absorption: Carrier molecule such as a protein or enzyme actively moves the drug across the membrane.
2) Passive absorption: Diffuse across a membrane from area of higher concentration to an area of lower concentration (Water Soluble Drugs).
(3) Pinocytosis: Cells engulf the drug particle across the cell membrane.
Think packman!
(4) Bioavailability is a subcategory of absorption. It is the percentage of the administered drug dose that reaches the systemic circulation.
For drugs taken orally bioavailability occurs only after the medication has been absorbed and metabolized by the liver.
Oral drugs that have a first pass hepatic metabolism may only have a bioavailability of 20-40% as opposed to I.V medications that have a 100% bioavailability.
Factors that alter Bioavailability are:
(1) The drug from (e,g tablet, capsule, sustained release, liquid, trans-dermal patch, inhalation).
(2) Route of administration.
(3) Changes in Liver metabolism caused by dysfunction.
(4) GI mucosa and motility.
(5) Food and drugs.
(6) Solubility: Drugs that are fat soluble are absorbed faster than water-soluble drugs.
Distribution: Movement of drug throughout the body typically on proteins (albumin).
(1) Therapeutic effect: Drug levels in blood to produce desired effect. (a) Too high = toxic
(b) Too low = decreased effect
Metabolism: Chemical reaction by with liver converts drug to inactive compound.
(1) Metabolism occurs in the Liver, Kidneys, lungs, plasma, and intestinal mucosa.
(2) A patient with liver disease may require a lower dose of a medication that is metabolized by the liver or a different medication that is not metabolized by the liver.
Excretion: Elimination of drugs from the body.
(1) Kidney excretes the inactive compounds from the body in the urine.
Half - Life: Time required for the body to eliminate 50% of the drug.
(1) Kidney, Liver disease and old age can increase the half-life increasing risk of toxicity.
Pharmacodynamics: Drug’s actions and effects within the body.
(1) Primary or desired effect.
(2) Secondary effects (side effects) – desired or undesired.
Physical dependence:
A compulsive need to use a substance repeatedly to avoid mild to severe withdrawal symptoms.
Psychological dependence:
A compulsion to use a substance to obtain a pleasurable experience.
Pharmacogenetic disorder:
A genetically determined abnormal response to normal doses of a drug.
Receptor:
A specialized macromolecule that binds to the drug molecule, altering the function of the cell and producing the therapeutic response.