biopharmaceutics Flashcards

1
Q

solutions
tabslets
capsules are examples of

A

oral formulations

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2
Q

for oral formulations, the absorption half life and bioavailability are dependent on

A

disintegration and dissolution rates

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3
Q

what factors affect dissolution rate (5)

A
aqueous solubility 
drug crystal size 
excipients (inactive ingredients)
-lubricants
-starches
tablet compression force 
enteric coatings or controlled release forms
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4
Q

dissolution is slower if the crystal size is

A

larger

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5
Q

incr in starch ____ dissolution

A

enhances, speeds up

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6
Q

incr in compression force _____ disintegration time

A

increases (so takes longer)

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7
Q
device for oral taking of drug: 
drug contained in core
semi permeable membrane on outside
permeable to water but not drug soln 
tiny pore that drug soln can come out of
A

osmotic pump: GI therapeutic system (GITS)

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8
Q

which order is constant rate

A

zero order

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9
Q

what order is iv infusion

A

zero order

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10
Q

large pills are excreted where (cant degrade in GI lumen)

A

in feces

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11
Q

why is buccal(topical / transfermal) admin advantage over swallowing a pill

A

avoids first pass effect

fast absorption

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12
Q

if a prodrug is a substrate for CYP2D6. a patient with a deficiency in this enzyme would have what happen to NR clearance of the prodrug

A

lower NR clearance

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13
Q

administration of a drug tablet w a glass of water instead of meal will do what to absorption half life

A

decr

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14
Q

meal with oral tablet will do what to absorption

A

incr absorption half life

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15
Q

carboxylate residues have an affinity for

A

OATP

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16
Q

what will decr the RN of a drug w carboxylate resideu

A

OATP inhibitor