Pharmacokinetics Flashcards

1
Q

what is pharmacokinetics?

A

the study of absorption
distribution
biotransformation
excretion of drug is called —
74
11-2-2025
10.41PM

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2
Q

what is Absorption ?

A

it is the process by which drug enters into the circulation (systemic/portal) from its site of administration across the biological membrane

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3
Q

why not IV + Intra-arterial ?

A

in this case drugs needs to be absorbed

rather they enter into the circulation directly

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4
Q

types of drug absorption ?

A

simple/passive

specialized

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5
Q

simple absorption process >

A

simple/lipid diffusion
filtration / aqueous diffusion

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6
Q

specialized transport process ?

A

active
facilitated
phagocytosis
pinocytosis
endocytosis

exocytosis

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7
Q

simple D VS Active D ?

A

80

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8
Q

Simple D all content ?

A

towards the electric gradient
no - energy + membrane + carrier protein

80

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9
Q

Active transport contents ?

A

against the conc/electrical gradient
energy + membrane + CP

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10
Q

facilitated diffusion example ?

A

Vitamin B12 absorption
tetracycline
glucose
pyrimidine
fat soluble vitamins

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11
Q

facilitated d definition?

A

diffusion of drug through a biological membrane
along the conc / electro-chemical gradient
with the help of a carrier protein

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12
Q

Simple D vs Faciliated D ?

A

80

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13
Q

route of administration for drug absorption?

A

IM>SC>O

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14
Q

lipid solubility and A ?

A

inc Lipid solubility = inc absorption

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15
Q

degree of ionization and absorption >

A

more I = more water soluble = less lipid soluble = less absorption

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16
Q

high dose & A ?

A

high dose = inc conc of drug

17
Q

dosage formulation ?

A

suspension > capsule > tablet

18
Q

why suspension more absorption <

19
Q

why tablet less absorption >

A

tablet —— disintegration —- dissolution —— absorption

20
Q

pk of drug & Absorption ?

A

less pKa
more ionization
drugs molecules draw water molecules from the solution duw=e to electrostatic charge
form hydrostatic shell which has larger size than the actual drug size
less penetration
more water soluble
less lipid soluble

20
Q

bioavailability def ?

90

A

it is defined as the fraction of unchanged drug
reching the systemic circulation

21
Q

sites of pre-systemic clerance ?

A

liver
lung
stomach
intestinal wall

22
Q

first pass metabolism ?

A

the elimination/metabolism of drug
that occurs after administration
but
before its enter into the systemic circulation

23
Q

drug distribution ?

A

it is the process by which drug reversibly leaves the blood stream and enters into the intestitium / cells of the tissues

23
Q

free drug vs PPB drug ?

24
Q

significance of PPB ?

25
Q

Volume distribution of PPB ?

A

less
as high PPB restricts a drug into the vascular compartments

26
Q

duration of action of PPB ?

A

long acting
as unavailable for metabolism / excretion

27
Q

volume of distribution defination ?

A

it is defined as the virtual volume pf plasma that
would contain the total body content of the drug
at a conc equal to the plasma

28
Q

Vd = ?

A

total amount of drug / plasma conc of drug
11-2-2025

11.46PM