pharmacokinetics Flashcards

1
Q

journey of drug through body

which bit is pharmacokinetic and what is pharmacodynamic

A
dose
plasma conc
target site
effect
clin outcome 

top 2 is kinetic
rest dyamic

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2
Q

LADME

A
liberation 
absorption
distribution
metabolism
elimination
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3
Q

at Cmax what is equal

A

abs and elim

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4
Q

Dl

A

initial dose

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5
Q

Cmax

A

max plasms conc

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6
Q

tmax

A

time to reach cmax

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7
Q

Vd

A

dist volume

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8
Q

C

A

plama conc

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9
Q

Dl=V x C is this right

A

yaa

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10
Q

admin is split into

A

systematic and topical

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11
Q

what uses circulatory system to distribute the drug

A

sys

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12
Q

which one is where the whole body is exposed to the drug

A

sys

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13
Q

parameters influencing abs

A

physiochem prop of drug

admin route

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14
Q

passive diffusion follows

A

first order kinetic

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15
Q

fac diffusion uses

A

channel/carrier protein

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16
Q

active transport will follow

A

michaelis-menten kinetics

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17
Q

different types of act trans

A

uniport
antiport
uniport coupled w a symport

18
Q

uniport

A

transport of a single drug

facilitate mode of diffusion accelarating a reaction that is thermodynamically favoured

19
Q

endocytosis

A

phagocytosis
pinocytosis
rec-med endocytosis

20
Q

phagocytosis

A

process of innate immune response and bridge between innate and acquired immune response

21
Q

pinocytosis

A

micropinocytosis

macropinocytosis

22
Q

Factors which influence bio availability

A

salt factor
bioequality
physiochem prop
co-admin of other drug
presence of cormobidity affecting abs sites
susceptible to gastric acid and digestive enzyme
degree of metabolism in gut mucosa and 1st pass

23
Q

salt factor

A

drugs not soluble therefore low bioavailability

increase sol, form as salt

24
Q

bioequality

A

ensure all drug has same bioav

25
Q

what needs to be same in bioeq

A

Cmax, tmax and AUC

26
Q

first pass effect s directly after ……… before reaching circ system

A

abs

27
Q

blood flow dependant on

A

exercise

shock

28
Q

drug binding

A

ionic bound

H bound

29
Q

in plasma protein binding the drugs are held in plasma by

A

albumin
lipoprotein
a-acid glycoprotein

30
Q

FU=

A

unbound conc/total drug conc

31
Q

dist vol

A

Vd=D/C

32
Q

Vd depend on

A

body weight

plasma protein bind

33
Q

Cap beds are

A

contiuous
fenestrated
sinusoid

34
Q

biotrasnfrmation in heptocytes

A

xeniotic
active metabolism
conjugate
excrete

35
Q

phase 1 included

A

func groups

36
Q

phase 1 has enzymes located in

A

SER

37
Q

enzymes in phase 1

A

oxygenases
reductases
hydrolytic enzymes

38
Q

what is a prodrug

A

compound after admin metabolised into active compound

39
Q

rate at which substrate is converted depnds on

A

turn over number

40
Q

phase 2 `

A

catalysed by transferase

@ low conc- sulfonation faster