1st module - basics Flashcards
Pharmacotherapeutics
Area of pharmacology that refers to the use of specific drugs to prevent, treat, or diagnose a disease.
Pharmacokinetics
Study of how the body absorbs, distributes, metabolizes, and eliminates the drug.
Pharmacodynamics
The analysis of what the drug does to the body, including the mechanisms by which the drug exerts its effect on target tissues.
Chemical names
generic name
trade name
Specific compound’s structure
The official name, typically derived from chemical name
Brand name, assigned to compound by the company.
Dose response curve
Dosage range of which a drug is effective. Allows understanding for how much drug is needed to initiate an effect as well as plateau.
Potency
Potency helps understand at what dose are we able to produce a response.
A more potent drug may require less of a compound to produce a certain response.
Therapeutic index
toxic dose/effective dose , closer to 1 the more toxic it is, the further from 1 the less toxic it is
Different ways for drug to enter
(enteral -towards the GI)
Oral, sublingual, rectal
(Perenteral)
Inhalation, injection, topical, transdermal
Oral
Advantages and disadvantages
advantage: easy, safe, convenient
Disadvantage: limited or erratic absorption of some drugs
Chance of first pass inactivation in liver
Example, analgesics
Sublingual
advantages rapid onset, not subject to first pass inactivation
Disadvantages drug must be easily absorbed from oral mucosa
rectal
pros alternative to oral route, local effect on rectal tissues
Cons poor or incomplete absorption, chance of rectal irritation
inhalation
pros, rapid onset, direct application for respiratory disorders, large surface area for systemic absorption
Cons, chance of tissue irritations, patient compliance sometimes s problem
injection
pros, provides more direct administration to target tissues, rapid onset
Cons, chance of infection if sterility not maintained
topical
pros, local effects on surface of skin
Cons, only good in treated outer layers of skin
transdermal
pros, introduces drug into body without breaking the skin, can provide steady prolonged delivery via medicated patch
Cons, drug must be able to pass through dermal layers intact
Tissue permeability distribution
highly lipid soluble drugs can potentially reach several body compartments or cells
large non-lipid soluble compounds will likely remain in the tissue they’re administers
Specific tissues ex) blood-brain barrier: limits the movement of drugs into the CNS
Blood flow distribution
Drugs circulating through the bloodstream have greater access to highly perfused tissues. Brain, Kidneys, and exercising skeletal muscle will receive more of the drug
Binding to plasma proteins distribution
Drugs distribution will be limited as some of the drug will form bonds with the circulating proteins and will therefore have no therapeutic effect
Binding to subcellular components distribution
Similar to binding to plasma proteins. Drugs may get “stuck” inside specific cells.
Half life
the amount of time required for 50% of the drug remaining in the body to be eliminated
Pharmodynamics
effect of drug
pharmokinetics
how the drug moves around in the body
surface receptors Link to
ion channels and directly to enzymes
ion channels
Receptors directly involved in cellular response by acting as an ion pore which changes the membrane permeability.
ex) Ach binding opens a pore allowing for NA+ to depolarize
ex) GABA in CNS allows for Cl- to enter.