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Biopharmaceutics & pK > Basic PK Principles > Flashcards

Basic PK Principles Flashcards

1
Q

pharmacokinetics is

A
  • the study of what the body does to the drug
  • i.e. what happens to the drug concentration as it moves through the body
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2
Q

Elimination includes these two things

A

Excretion and metabolism

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3
Q

Bioavailability is the measurement of

A

the extent and rate of absorption of a drug or the fraction of the administered dose that reaches systemic circulation

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4
Q

what a drug does to the body including mechanism of action

A

Pharmacodynamics

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5
Q

Pharmacogenetics is the study of…

A

the differences in response as a result of genetic differences in populations

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6
Q

the ratio of the dose of drug producing an undesirable effect to the dose producing the desired therapeutic effect is known as…

A

Therapeutic index or the margin of safety of a drug

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7
Q

A drug with a high therapeutic index has a small or large margin of safety

A

Large Margin of safety

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8
Q

drugs with low margin of safety require this and why

A

monitoring of plasma concentration levels to minimize potential toxic effects due to increases in plasma concentration

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9
Q

Pharmacokinetics is used to determine these 6 things

A
  1. Bioavailability (rate and extent of drug absorption)
  2. drug interactions
  3. dosing regimen
  4. altered dosing regiment for comorbid conditions e.g. liver disease/renal impairment
  5. dose adjustments for individual pt variables such as obesity, diet, smoking
  6. quantify or predict drug residues in tissues (animals meat producers)
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10
Q

Represents a grouping of tissues or a volume of fluid representing the body

A

Compartment

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11
Q

why is plasma a good reference tissue (2 reasons)

A
  • easy to sample
  • comes into contact will all tissues
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12
Q

what is the driving force for pK

A

the speed with which drug is cleared

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13
Q

what determines whether a one, two or multicompartment model is used

A
  • the rate at which drug is distributed
    • slow - more compartments
    • fast - 1 compartment
  • how much is known about the drug
  • what you are trying to understand i.e. 1 compartment for dosing; 2 or multicompartment for drug interactions or distribution in tissues
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14
Q

the Central Compartment is made up of

A

well profused tissue like heart, kidneys, plasma

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15
Q

Fat, muscle and cerebrospinal fluid make up this compartment

A

Peripheral Compartment

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16
Q

which compartment model is the most highly used

A

one compartment model

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17
Q

what assumptions are made in the compartment models (2)

A
  • that drug distributes instantaneously
  • that drug distributes linearly to all tissues
  • the compartment is well stirred and homogeneous i.e. the same concentration throughout the compartment
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18
Q

how does assuming linear distribution of drugs to tissues help in pK modeling

A

allows for the use of a reference tissue such as plasma, saliva or urine

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19
Q

most drugs follow Zero or First order kinetics

A

First

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20
Q

What is t1/2? (2)

A
  • half life of a drug
  • loss of drug from the body
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21
Q

what is t½ = 0.693/K

A

half life

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22
Q

what are the two calculations by which half life can be calculated

A
  1. t½ = 0.693/K where K is the slope or elimination rate constant
  2. t½ = 0.693 Vd/Cl where Vd = volume of distribution and Cl = clearance
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23
Q

simplest pK model describing distribution and elimination

A

one compartment model

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24
Q

when is IV bolus commonly used in pharmacokinetics

A

when trying to develop a model for drug distribution or dosing

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25
Q

why is IV bolus administration commonly used in pK modeling (3 reasons)

A
  • because absorption is immediate
  • there are no input kinetics
  • behaviour of drug determined based solely on distribution and elimination
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26
Q

Absorption, Distribution, Metabolism and Execretion are part of pharmacokinetics or pharmacodynamics

A

Pharmacokinetics

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27
Q

what are the parameters of compartment models (2)

A

volumes and rate constants

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28
Q

aside from plasma, what are two other reference tissues used in pK analysis

A

Urine and saliva

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29
Q

one compartment models are commonly used for:

A
  • dose determination
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30
Q

When are 2 or more compartment models used (2)

A
  • mechanism of drug interaction
  • Tissue concentration
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31
Q

Pharmacokinetic models allow for the prediction of

A

time course of drug concentration or the amount in one or more compartments

32
Q

What is the equation for the amount in body (Ab) for a one compartment model

A

Ab = Cp x V

Where Cp is concentration of drug in the compartment

V is the volume of the compartment

33
Q

What is Cp

A
  • Plasma Concentration or concentration in the compartment
  • Cp = D/V
34
Q

Pharmacodynamics refers to the relationship of drug concentrations to

A

drug effect

35
Q

The EC50 refers to the drug concentration at which

A

one half of the maximum effect is achieved

36
Q

The therapeutic range is the range of plasma drug concentrations that will

A

Most likely result in desired drug effect and minimal risk of drug toxicity

37
Q

The most important concept in therapeutic drug monitoring is

A

drug effect is related to plasma concentration

38
Q

Factors (3) that may result in variability in plasma drug concentrations after the same drug dose is given to different patients includes variations in

A
  • Drug absorption
  • Genetic differences in metabolism
  • Body weight
  • comorbid conditions e.g. renal insufficiency,
39
Q

An example of a situation that would not support therapeutic drug monitoring with plasma drug concentrations would be one in which

A

The toxic plasma concentration is much higher than the therapeutic concentration range

40
Q

For a drug with a narrow therapeutic index, the plasma concentration required for therapeutic effects is near the concentration that produces toxic effects. (True/False)

A

True

41
Q

The central compartment includes fat tissue, muscle tissue, and cerebrospinal fluid. (True/False)

A

False

42
Q

The theoretical volume required to account for all of the drug in the body, if the concentration in all tissues is the same as the plasma concentra tion, is defined as the

A

Volume of distribution

43
Q

Vd = X or D/Cp

where X or D = drug dose

Cp = drug concentration in plasma at time zero

A

Volume of Distribution

44
Q

Are compartment models deterministic or probabalistic, why?

A

deterministic

because the observed drug concentration determines the type of compartment model required for pK

45
Q

what is the basic concept in a two compartment model (3)

A
  • The drug profuses quickly into the first compartment (central compartment) (blood, hear, liver, kidneys)
  • then drug profuses from central to peripheral more slowly establishing equilibrium
  • elimination occurs from first compartment
46
Q

When volume of distribution (Vd) is large (2)

A
  • drug is distributed in a large volume i.e. not plasma bound
    • bound to proteins of extravascular tissue or the peripheral comparment tissues
  • Plasma concentration is low
    • may need to have a load dose
    • larger dose required to get target plasma concentration
47
Q

when volume of distribution is low (2)

A
  • drug is mainly bound to plasma, i.e. limited distribution
  • Cp is high
    • if highly bound to plasma less drug ciruclating in body
      • dosing regimen is important as toxic effects or drug interactions can be seen
48
Q

drugs which are lipid soluble have higher or lower Vd than hyrdophilic or water soluble drugs

A

Higer Vd

49
Q

is free or bound drug active

A

free drug

50
Q

what are common pharmacokinetic parameters (4)

A
  • Volume of Distribution (Vd)
  • Clearance (Cl)
  • Bioavailability
  • 1/2 life (t1/2)
51
Q

what is clearance

A
  • the volume of blood or plasma cleared of drug per unit time
52
Q

What pk parameter (A,D,M or E) does clearance describe

A

Elimination

53
Q

Is clearance a dependent or independent pK parameter

A

Independent

54
Q

how is clearance calculated? (2)

A
  • Cl = K x Vd or
  • Cl = K / Cp where Cp = D/Vd or amt in body/Vd
55
Q

what are 2 reasons why is Vd useful

A
  • because you can’t measure amount in body
  • used to calculate the dose required to get the target plasma concentration
56
Q

what is the formula for calculating slope

A

Slope = log y2-y1/ x2-x1

57
Q

The steeper the slope the higher or lower K and t1/2?

A

K is higher; t1/2 lower

58
Q

K or the elimination rate constant can be calculated using slope by the following formula

A

k = - slope (2.303)

59
Q

when the amount of drug lost equals the amount of durg administered

A

steady state concentration

60
Q

Poor bioavailiability may be the result of these 4 things

A
  • poor solubility
  • incomplete absorption in GI tract
  • metabolism in lining of GI tract
  • first pass metabolism
61
Q

Bioavailability is

A

the fraction of drug reaching systemic circulation after administration

62
Q

how is bioavailability calculated

A

Bioavailability (F) = (AUC oral/AUC iv) x (dose iv/dose oral)

63
Q

how is bioavailability often compared (2)

A
  • by comparing AUD oral vs. IV in cross over study design
  • if the dose is not the same then dose adjust
64
Q

Maintenance dose rate is calculated by:

A

Target Cp x Clearance

65
Q

Loading dose is calcuated by

A

Css (mg/l) x Vd (L)

where Css is the target drug concentration

66
Q

Area under the curve is calculated by

A

AUC = Cp0/K

where 0 = time zero; plasma drug concentration plotted over time

67
Q

Elimination from the body occurs by these two processes

A

biotransformation and excretion

68
Q

Elimination generally occurs wehre

A

liver and kidneys

69
Q

Elimination processes generally follow first or zero order kinetics

A
  • First order kinetics
    • i.e. the rate of elimination is directly proportional to the amount of drug in the body
70
Q

Absolute bioavailability is

A

F = Auc (oral) / Auc (iv)

71
Q

rate of urinary excretion (equation)

A

KuAb = DAu/Dt

where Au = amount of drug excreted in uring

Ku = urinary elimination rate constant

72
Q

Besides direct measurement in plasma, describe another way that drug plasma concentration can be obtained

A
  • by back extrapolating on a concentration vs. time graph
  • the intersect with the y axis is the T0 concentration
73
Q

the larger the Vd the larger or smaller the dose must be?

A

Larger, directly proportional

74
Q

how is total clearance calculated

A 
Clt = Clr + Clm + Clb + Cl other, where:
Clt = total body clearance (from all mechanisms, where t refers to total)

Clr = renal clearance (through renal excretion)

Clm = clearance by liver metabolism or biotransformation

Clb = biliary clearance (through biliary excretion)

Clother = clearance by all other routes (gastrointestinal tract, pulmonary, etc.)

75
Q

assumes instantaneous distribution, linear distribution in all tissues, and instantaneous elimination

A

one compartment model

Biopharmaceutics & pK (7 decks)

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