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26 Cards in this Set

  • Front
  • Back
Branches of pharmacology
pharmacodynamics - action of drugs on body
pharmacokinetics - fate of drugs in body
toxicology - study of undesirable, adverse effects of drugs
pharmacogenetics - genetic factors contributing to drug response/outcomes
drug size and molecular weight (MW)
MW b/w 100 to 1000
- too small: drugs not selective
- too large: poorly absorbed & distributed
ex of drug size & MW and action in body
BBB prohibits access of large hydrophilic molecules into CNS
types of drug-receptor bonds
1. covalent bonds (usual irreversible)
2. electrostatic bonds (b/w cation/anion)
3. weak H2, van der Waals, hydrophobic bonds
What are the main factors determining the movement of drugs in the body
charge of drug and medium
Fick's law determines what?
movement of molecules through membranes and other lipid structures
Many drugs are found to be either:
weak acids or weak bases
What determines the fraction of the molecules (drug) that are charged/uncharged, as well as the absorption of the drug across the lipid membrane
the pH of the medium
What does the Henderson-Hasselbalch equation predict?
The propensity of a drug to carry a charge under different physiological conditions (helps determine absorption/excretion)
Ionized drugs are more:
Non-ionized drugs are more:
water soluble
lipid soluble
Since membranes are composed of lipids, what types of drugs are absorbed, and which are excreted?
1. non-ionized - absorbed
2. ionized - excreted
The ionized/non-ionized form of drugs are determined by:
1. pH of environment
2. whether drug is weak acid or weak base
An acid in an acid environment favors:
absorption (lots of acidic form, so they shift to non-ionized form; non-ionized form favors absorption)

AAA
An acid in an alkaline environment favors:
excretion (lots of nonprotonated molecules, so shift to the ionized form to donate protons; ionized form favors excretion)

ABE
A base in an acidic environment favors:
excretion (lots of nonprotonated molecules, so they shift in direction of ionization; ionized form favors excretion)

BAE
A base in a basic/alkaline environment favors:
absorption (lots of protonated molecules, so they shift in the direction of non-ionized form; non-ionized form favors absorption)

BBA
Henderson Hasselbach equation
log (protonated/unprotonated) = pKa - pH
Most drugs are freely filtered at the ________, but lipid-soluble drugs can be rapidly reabsorbed from the _______________.
glomerulus; tubular urine
Weak acids are _____ faster in basic urine; and ______ faster in acidic urine.
excreted; reabsorbed
Weak bases are excreted faster in _____ urine; and reabsorbed faster in _____ urine.
acidic; basic
Acidify urine by giving
ammonium chloride
alkalinize urine by giving
sodium bicarbonate
Fick's law of diffusion
rate = (c1-c2) x (perm coefficient/thickness) x area

interpretation: drugs absorbed faster from organs w/ large SA and thin membranes
What other types of permeations, aside from pH, determines absorption
- aqueous diffusion
- transport by special carriers
- endocytosis/ pinocytosis
1. Which of the other types of permeations is governed by Fick's law?

2. Which of the other types is not?
1. aqueous diffusion

2. transport by special carriers
What criteria must be considered in determining route of administration:
1. drug properties and profiles
2. drugs site of action
3. condition and age of patient
4. rapidity and duration of drug effect required
5. convenience, cost, availability