ADME Flashcards

1
Q

Response of drug is fucntion of this

A

concentration of drug at the receptor site

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2
Q

plasma concnetraion above this level will produce an effect

A

Minimum Effective Concentration

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3
Q

factors that controll the concentration and duration of action

A

Absorption, Distribution, Extent and rate of transformation, metabolism and excretion

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4
Q

moves things down elerctrochemical gradient

A

passive diffusion, facilitation diffusion

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5
Q

transfer that does not require energy

A

passive diffusion

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6
Q

transfe that does not saturate

A

passive diffusion,

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7
Q

transfer that can saturate

A

facilitated and active transport

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8
Q

transport of large ionized water soluble molecules

A

active transport

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9
Q

transport in which driving force is hydrostatic or osmotic pressure difference

A

filtration

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10
Q

transfer that can be selective or non-selective

A

endocytosis

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11
Q

transfer selective and inhibited by closely related chemicals

A

facilitated diffusion and active transport

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12
Q

defintion of secondary energy

A

coupled to another compounds electrochemical gradient

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13
Q

most common transporter fo this family is p-glycoprotein (MDR1)

A

ABC (ATP binding-cassette) superfamily

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14
Q

supefamily that moves substances in and out of cells

A

SLC (solute carrier) superfamily

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15
Q

process by which a drug moves from site of administration fo plasma

A

absorption

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16
Q

how most drugs are absorbed

A

passive diffusion

17
Q

disadvantages of oral drugs

A

destroyed by stomach, first pass metabolism, veriable absorption rate

18
Q

measure of the fraction of an adminsterd dose that is absorbed into circulation

A

bioavailability

19
Q

things that alter bioavailability

A

disintegration rate, dissolution rate, solubiliyt, coating

20
Q

disadvantages of iv drugs

A

overdose, cannot take back, usnutibale for chronic, dmaage to tissue

21
Q

disadvante of topical drugs

A

local only, large surface area may produce system/toxic response

22
Q

proces by which drug moves from the plasma to other sites in the body

A

distribution

23
Q

factors that affect distribution

A

tissue perfusion rates, plasma protein binding, partitioning between plasma and tissue

24
Q

perfusion rate in muscles

A

intermediate

25
Q

effect of drug bound to plasma

A

cannot cross pm, reduces [free], inert, cannot be filtered by kidney

26
Q

effect of tisssue proteins

A

compete with binding proteins in plasma

27
Q

defintion of volume of distribution

A

Vd = total amount in body/total concentration in plasma

28
Q

mechanisms for terminating drug action

A

stoarge, excretion, biotransformation

29
Q

redistribution phase in which drug distributes to tissue wth low flows

A

second phase

30
Q

transport used for reabsorption

A

facilitated transport and passive diffusion

31
Q

renal clearence defintion

A

CLr = CuVu/Cp

32
Q

when elimiated drugs are reabsorbed

A

enterohepatic circulation

33
Q

biotransformation usually does this to the polarity

A

more polar

34
Q

biotransformation may also do these things

A

produce and active or inactive drug, maybe required to activate a drug

35
Q

Describe pahse 1 Rxn

A

funtional group added via oxidation, metabolite more polar and water solubel, metabolit less active

36
Q

Describe a phase 2 reaction

A

sythetic conjugation addes large molecule, glucuronidation, drug inactivated

37
Q

Common sites of biotranformation

A

liver (VIP), GI tract kidney, lung, skin, SER - phase II