Issar- Drug Excretion Flashcards

1
Q

bowmans capsule is very porous for filtration. so will drug bound to a protein be filtered thru here?

A

no. because it is to big

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2
Q

active tubular secretion occurs in the proximal tubule. since it is a an active process, what may occur?

A

competitve inhibition of the secretion of one compound by another (ex. penicillin competes with probenecid, which is a gout drug)

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3
Q

what is used to measure renal clearance?

A

inulin

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4
Q

in order to get reabsorbed what must the non-ionized form have a sufficient amount of?

A

lipophilicity

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5
Q

what is the equaiton for rate in= rate out?

A

(CLr)(Cp)=(Qu)(Cu)

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6
Q

if a drug is only partially reabsorbed what is the clearance drug: clearance inulin ration?

A

ratio<1

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7
Q

if the ratio, CLdrug: CLinulin > 1. what is the probable mechanism of renal excretion?

A

actively secreted

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8
Q

what ratio is necessary for the drug to be only filtered?

A

CLdrug: CLinulin =1

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9
Q

what is the equation for renal clearance?

A

CLr= (Qu*Cu)/ Cp

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10
Q

if the renal clearance for a drug has decreased, what can be implied about the plasma concentration of that drug?

A

it has increased

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11
Q

what type of excretion do strongly polar groups, and high m.w compounds go through? (m.w. more than 500)

A

biliary excretion

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12
Q

enterohepatic circulation works to prolong the duration of action of certain drugs. how is this done?

A

creates reservoir of recirculating drug by becoming hydrolyzed in gut by beta-gluronidase - available for reabsorption

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13
Q

what factors affect biliary secretion?

A

liver disease or injury, age, chronic administration of drugs increase bile flow, competition between drugs

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14
Q

are highly soluble drugs faster at being removed via pulmonary excretion?

A

no. they are removed slower (NO is not very soluble in blood and is excreted rapidly)

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15
Q

what is excretion in sweat and saliva dependent on?

A

diffusion of non-ionized form of drug

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16
Q

in milk, the presence of drug is dependent on?

A

maternal blood concentration, plasma protein binding, lipid solubility and pKa

17
Q

what prevent toxic drugs from entering the CNS?

A

P-glycoprotein

18
Q

what is the overall renal excretion controlled by?

A

what happens in the tubules

19
Q

what drug is extensively secreted, with clearance values approaching the renal plasma flow rate of 425-650ml/min?

A

p-aminohippuric acid (PAH)

20
Q

what else besides inulin is used to estimate the GFR

A

creatinine - is freely filtered and not reabsorbed

21
Q

what does it mean if the plasma creatinine increases?

A

the Cl(creatinine) has decreased and kidney function has decreased

22
Q

what do drugs like quinidine, ketoconazole, and verapamil do to the drug digoxin?

A

they increase the serum concentration of digoxin by inhibiting activity of Pgp (requires Pgp for excretion)

23
Q

what do drugs like rifampin or St. John’s wart do to digoxin?

A

they decrease serum concentration by inducing Pgp activity