Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
36 Cards in this Set
- Front
- Back
disposition of chemicals |
absorption, distribution, biotransformation, elimination |
|
disposition |
determine concentration at the site of action and dictates the potential for adverse events to occur |
|
main sits of absorption |
GI tract, lungs, and skin |
|
absorption |
the transfer of a chemical from the site of exposure into the systemic circulation; enters bloodstream |
|
rate of absorption depends on |
concentration, area exposed, characteristics of the layer, blood circulation, phisiochemical properties |
|
amphiphillic molecules |
contains both hydrophobic and hydrophobic moieties |
|
saturated fatty acids |
maximizes London dispersion interactions; melting point increase b/c of straight chain |
|
unsaturated fatty acids |
predominantly cis configuration, melting point is lower b/c of bent chain |
|
integral/intrinsic proteins |
associate tightly with the membrane through the hydrophobic interactions |
|
lipid-linked protiens |
anchored to membrane through covalently attached lipids |
|
peripheral/extrinsic proteins |
loosely connected to membranes and can be dissociated by mile procedures |
|
passive process |
high concentration to low concentration |
|
translocate |
low concentration to high concentration |
|
paracellular diffusion |
small hydrophillic molecules travel through aqueous pores |
|
transcellular diffusion |
hydrophobic molecules diffuse across the lipid domain |
|
negative logP |
water soluble |
|
positive logP |
lipid soluble |
|
facilitated diffusion |
transportation where substrate is not moved against a concentration gradient, and the transport process does not require input energy |
|
active transport |
movement against concentration gradient; saturability at high concentration selectivity of certain structures; requires energy |
|
ATP binding cassette transporters (ABC) |
binding and hydrolysis of ATP provides the energy required to move their substrates across memebranes |
|
lipid soluble compounds move by |
diffusion |
|
water soluble chemicals move by |
diffuse transcellular pores and/or across the cell membrane |
|
highly ionized/hydrophillic xenobiotics move by |
specialized membrane carrier systems |
|
absorption increases with ______ particle diameter |
decreasing |
|
pH of stomach |
2 |
|
pH of small intestine |
6.6 |
|
weak organic acids are absorbed more through the stomach or small intestine |
stomach |
|
organic bases are absorbed more through the stomach or small intestine |
small intestine |
|
factors influencing absorption through the skin |
strength of outer-most skin; hydration of the outer-most skin; temperature; solvents size and physical properties |
|
caustic agents _____ skin permeability |
increase |
|
increase in temp will ____ dermal penetration by ____ blood flow |
increase; increase |
|
intravenous route |
introduces toxicant directly to bloodstream |
|
factors affecting distribution |
binding to plasma proteins; special barriers; distribution to storage sites that are not target sites; export from cells |
|
two organs that accumulate chemicals |
liver and kidneys |
|
detoxication |
biotransformation that eliminates ultimate toxicant or prevents its formation (liver and kidney) |
|
excretion |
physical mechanism of the removal of xenobiotics from the blood and their return to the external environment (urine; feces; lungs) |