Exam 3 absorption Flashcards

1
Q

which route of administration avoids the need to cross the biological membrane in order to reach the systemic circulation

A

intravaneous

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2
Q

which route of administration avoids the need to cross the biological membrane in order to reach the CNS

A

intraspinal

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3
Q

the 6 factors that determine movement across membrane

A

characteristics of the membrane, mechanism of passage across mem, dwell time of drug-membrane interface, physicochemical characteristic of drug, ph of environment and surface area of absorptive surface

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4
Q

T/F the most oral drug absorption occurs in the small intestine

A

True

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5
Q

the inner walls of the small intestine are covered by numerous folds called

A

plicae circulares-folds of Kerckring

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6
Q

the small intestine folds contain tiny projections called

A

villi x30 and microvilli x600

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7
Q

the small intestine folds increase

A

the surface area by 3 times

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8
Q

the transit time to the small intestine influences the

A

peak concentration

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9
Q

what impact would a drug that speeds up stomach emptying have on the peak concentration for acetaminophen

A

increase peak concentration

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10
Q

increased stomach emptying does what to the half life

A

decreases

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11
Q

increased rate of elimination does what to the half life

A

decreases

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12
Q

decreased half life does what to the peak concentration

A

increases

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13
Q

what are the mechanisms by which drugs cross the biological membranes

A

paracellular, transcellular, carrier protein, endocytosis

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14
Q

what does paracellular mean

A

travels between cells, small molecules

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15
Q

what does transcellular mean

A

travels through the cell

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16
Q

that does carrier protein mean

A

requires a transpotein to move them through cell

17
Q

what does endocytosis mean

A

a vesicle is created to carry though cell

18
Q

what is the driving force for movement of drug via paracellular and transcellular

A

concentration gradient- high to low

19
Q

facilitated diffusion and active transport are both examples of

A

carrier-mediated transport

20
Q

how much of drugs are predominantly by passive transcellular diffusion

A

95%

21
Q

transcellular permeability can be increased by

A

removing charged (ionized) groups, increasing lipophilicity and reducing size

22
Q

passive diffusion across membrane is dependent on

A

pKa and pH

23
Q

Base: pKa < pH

A

base passes through

24
Q

Base: pKa > pH

A

conjugated base passes

25
Q

Acid: pKa > pH

A

conjugated acid passes

26
Q

Acid: pKa < pH

A

acid passes

27
Q

paracellular diffusion allows what to pass

A

small and polar molecules

28
Q

what may open the junction in paracellular diffusion

A

toxins

29
Q

for a drug which undergoes passive diffusion, the rate of transport across the membrane should increase as the concentration

A

increases

30
Q

Carrier-mediated mechanism of facilitated diffusion uses

A

the concentration gradient

31
Q

T/F carrier-mediated transport required energy

A

FALSE, concentration gradient does not need energy

32
Q

carrier-mediated mechanism of active transport uses

A

energy to go against concentration gradient

33
Q

what exists on both the apical and basolateral membrane of intestinal and other cells

A

transport proteins

34
Q

if a drug is a substrate for pgp in the enterocyte, how would co-administration with another drug that inhibited pgp change the amount of drug that entered the systemic circulation

A

increases

35
Q

consequences of the efflux transporter P-glycoprotein

A

limited drug absorption, enhanced drug elimination, limited distribution

36
Q

endocytosis is typically for

A

large molecules

37
Q

T/F there are different mechanisms of endocytosis depending on size

A

TRUE