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Pharmacokinetics

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Title: Pharmacokinetics


1
Pharmacokinetics
  • Asmah Nasser, M.D.

2
Pharmacokinetics
  • Pharmacokinetics is the quantitative study of
    drug movement in, through and out of the body

3
What Happens After Drug Administration?
  • Absorption
  • Distribution
  • Metabolism
  • Elimination /Excretion

4
Important factors to know
  • Factors affecting absorption
  • Concept of ionization , pKa and pH
  • Henderson Hassel Balch equation
  • Bioavailability , Bioequivalence , AUC
  • Distribution , volume of distribution (Vd),
    redistribution
  • Plasma protein binding

5
Important factors to know
  • Metabolism (biotransformation) , CYP 450 etc
  • Excretion
  • First and zero order kinetics of elimination
  • Plasma Half life
  • Clearance
  • Steady state ,loading and maintenance dose
  • Therapeutic drug monitoring
  • Pharmacokinetic calculations

6
Absorption
  • After a drug is administered, how does it reaches
    site of action?
  • Absorption is the transfer of a drug from its
    site of administration to the blood stream. In
    order to reach their site of action, a drug has
    to pass through several membranes

7
Transport
  • A. Passive diffusion Concentration gradient
    across membrane is the driving force for movement
    of drug molecule across the membrane
  • Small size, water soluble drug molecule
    penetrate through aqueous channels or
    paracellular spaces Filtration few drugs does
    this
  • Lipid soluble drugs readily pass through membrane
    by dissolving in membrane .many drugs does this
  • B. Active Transport
  • Movement occurs against the concentration
    gradient and needs energy like ATP

8
Factors that affects absorption
  • The particle size Smaller is better
  • concentration gradient
  • Surface area and vascularity of that area
  • Lipid solubility / Water solubility
  • Nature of the drugacidic or basic
  • Ionized or non ionized
  • The pH levels on either side of cell membrane
  • pKa of the drug

9
Lipid/Water solubility
  • Once in solution, drugs exist as a mixture of two
    interchangeable forms
  • 1. Water-soluble is the ionized or electrically
    charged formCannot cross membrane
  • 2. Lipid-soluble is the non ionized, or uncharged
    form.Can cross membrane

10
Concept of ionizationcontinued
  • We know most of the drugs are either weak acid
    or a weak base and when dissolved in body
    fluids, some or all of a drugs molecules become
    ionized/unionized

HA H A-
BH
B H
11
Concept of ionizationcontinued
  • What percentage is ionized /unionized determined
    by following factors
  • 1.Whether the drug was an acid or a base.
  • 2. Whether it is dissolved in an acid or base
    medium (Eg Stomach or intestine ?) i.e pH of the
    medium.
  • 3. And also the pKa of the drug.

12
Role of pH in ionization of a Weak base
  • As pH increases, a weak base will become more and
    more unionized, lipid soluble and better absorbed
  • As pH decreases, a weak base will become more
    and more ionized, lipid insoluble, and will not
    be absorbed. Also becomes more water soluble and
    better excreted.

13
Role of pH in ionization of a Weak base
100
75
50
of Unionized form
25
0
1
14
pH of the medium
14
Role of pH on ionization of a Weak Acid
  • As pH increases, a weak acid will become more
    and more ionized , lipid insoluble and will not
    be absorbed. Also becomes more water soluble and
    better excreted .
  • As pH decreases, a weak acid will become more and
    more unionized , lipid soluble and better
    absorbed .

15
Role of pH in ionization of a Weak acid
100
75
50
of Unionized form
25
0
1
14
pH of the medium
16
Question
  • Aspirin is an acidic drug.
  • In the stomach, is it mostly in the ionized or
    unionized form?

17
Moral of the story...
  • Acidic drugs are Absorbed best in Acidic
    environments

Basic drugs are Best absorbed in Basic
environments
18
So...
To ? absorption of an basic drug acidify the
environment
To ? absorption of an acidic drug alkalanize the
environment...
This concept is very important in treatment of a
drug poisoning
19
pKa
  • pKa is equivalent to the pH at which 50 drug
    is ionized and 50 is unionized.Remember this
    point
  • pKa Is the negative logarithm of acidic
    disassociation constant of the weak electrolyte
    not necessary to know

20
100
75
of Unionized form
50
25
0
1
14
pH of the medium
pKa
21
Henderson-Hasselbalch equation
  • The ratio of lipid-soluble form to water-soluble
    form for a weak acid or weak base is expressed by
    the Henderson-Hasselbalch equation
  • The Henderson-Hasselbalch equation relates the
    ratio of protonated to unprotonated weak acid or
    weak base to the molecule's pKa and the pH of the
    medium as follows

22
Henderson-Hasselbalch equation
  • pH pKa log (Unprotonated form)
  • (Protonated form)
  • For a weak acid, if pH pKa is low it will be
    more non-ionized and better absorbed
  • For a weak base if pH pKa value is high it
    will be more non-ionized and better absorbed

23
pH-pKa -2 -1 0 1 2
Weak acid nonionized 99 90 50 10 01
Weak base nonionized 01 10 50 90 99
24
Question
  • 1. The pKa of acetylsalicylic acid is 3.5. What
    percentage of the drug is in an absorbable form
    in the stomach at pH of 1.5?A. 0.1B. 1C.
    10D. 90E. 99

25
Question
  • The greater proportion of the dose of a drug
    administered orally will be absorbed in the small
    intestine. However, on the assumption that
    passive transport of the nonionized form of a
    drug determines its rate of absorption, which of
    the following compounds will be absorbed to the
    least extent in the stomach?
  • a. Ampicillin (pKa 2.5)
  • b. Aspirin (pKa 3.0)
  • c. Warfarin (pKa 5.0)
  • d. Phenobarbital (pKa 7.4)
  • e. Propranolol (pKa 9.4)

26
Summary
  • A drug molecule carrying an electrical charge is
    said to be Ionized
  • Lipid-soluble is the non ionized, or uncharged
    form.Can cross membrane
  • Percentage of ionized drug depends on
  • 1.Whether the drug was an acid or a base
  • 2. Whether it is dissolved in an acid or base
    medium (Stomach or intestine ?) i.e pH
  • 3. And also the pKa of the drug
  • As pH increases, a weak base will become more and
    more unionized ,lipid soluble and better absorbed
  • As pH decreases, a weak acid will become more and
    more unionized ,lipid soluble and better absorbed

27
Summary
  • pKa is equivalent to the pH at which 50 drug
    is ionized and 50 is unionized
  • For a weak acid if pH pKa is low it will be
    more nonionized and better absorbed
  • For a weak base if pH pKa value is high it will
    be more nonionized and better absorbed
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