Ch. 1 - Drug Action Flashcards
Drug
any chemical substance that affects living systems by changing their structure or function
3 phases of drug action:
- ) Pharmaceutic phase
- ) Pharmacokinetic phase
- ) Pharmacodynamic phase
**Pharma(ceutic) phase****
(Dissolution)
- Solid form: needs to disintegrate
* Tablet > disintegration > dissolution - Liquid form
Pharma(ceutic) phase: Enteric Coated
RESIST disintegration in STOMACH ------------------------------------------------------------- DISINTEGRATES in the SMALL INTESTINE \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ should NOT be crushed
Pharma(ceutic) phase cont…
Food in GI tract:
* may interfere * may enhance
**Pharmaco(kinetic )Phase*****
- kinetic* = means ‘movement’
- process of drug movement to achieve drug action
- ) Absorption
- ) Distribution
- ) Metabolism (biotransformation)
- ) Excretion (elimination)
Pharmaco(kinetic )Phase: Absorption
Gastric absorption influnced by:
*food, gastric pH
Absorption cont.
bioavailability (subcategory)
* % of drug dose that reaches the system circulation * Ex: taking it orally compared to intravenously
Pharmaco(kinetic )Phase: (1) Distribution
drug becomes available to body fluids and body tissues
Distribution (2)
Drug enters bloodstream –> rapidly carried to organs with blood supply
Distribution (3)
Influenced by:
- blood flow - drug's affinity to the tissue - protein-binding effect
Pharmaco(kinetic )Phase: Protein-binding Effect
- portion of the drug that is bound (to protein):
* inactive (not available to receptors) - Unbound portion:
* free (active) = pharmacologic effect
3.) Metabolism (biotransformation):
IF NOT water soluble = biotransformation occurs to convert to a more water soluble form
Metabolism (biotransformation): cont..
Age, hepatic disease = slow down ability
———————————————————-
Liver = primary source of metabolism
Half-Life:
-time it takes for 1/2 of drug to be eliminated from body
(Ex:)
Half-life: 4 hrs
{Every 4 hr interval drug conc. decreases 50%}
*Initial (8am) = 100% (500mg)
*After 4 hrs = 50% (250mg)
*After 8 hrs = 25% (125mg)
*After 12 hrs = 12.5% (62.5mg)
*After 16hrs = 6.25% (31.25mg)
4.) Excretion (Elimination):
Kidney function affected by:
*age, kidney disease
Pharmacodynamic phase**
drug concentration & its effects on the body
*Mechanism of action
Drug Response: Primary or Secondary
diphenhydramine (Benadryl)
- Primary effect:
- treat symptoms of allergy - Secondary effect:
- CNS depression –> drowsiness
Onset:
time it takes to reach minimum effective concentration (occur)
Peak:
drug reaches its highest blood concentration (level)
Duration:
length of time drug has a pharmacologic effect
Receptor Theory:
- drugs most commonly form a chemical bond with specific receptors in the body
* lock & key relationship
Agonist:
interacts with receptor to produce a response
Antagonist:
inhibits or prevents action of an agonist or blocks a response
Therapeutic Range (Window):
Low Therapeutic Index (TI) = narrow margin of safety
———————————————————
High TI = wide margin of safety
Peak level:
highest plasma concentration at a specific time —-(measures rate of absorption)
Trough level:
lowest plasma concentration (measures rate of excretion)
Loading Dose:
Large initial first dose when an immediate drug response is desired
**Ex: Z-pack = take 2 doses first day, then 1 dose after that
Side effects:
acts on other tissues besides specific intended issue
Adverse effects:
unpredictable (idiosyncratic) adverse effects
-allergic hypersensitivity d/t individuals immune system
————————————————————–
Severe allergic reaction > anaphylaxis > resp./circ. collapse > death
Toxicity
- ALL drugs are able to be toxic if dosage is high enough*
- related to dosage
Teratogenic Effect:
congenital defect in fetus whose mom took drug during pregnancy
Drug Tolerance:
resistance to effect of drug
-need higher dosage/frequency to produce desired effect
Placebo Effect:
Psychological benefit from taking a chemical compound
- Persons feels that the pill will make them feel better