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PRESENTED BY,
ABITH BABURAJ
 The study of the disposition of a drug
 The disposition of a drug includes the processes of ADME
 Absorption
 Distribution
 Metabolism
 Excretion
 Drug concentration at sites of action influenced by several
factors, such as:
◦ Route of administration
◦ Dose
◦ Characteristics of drug molecules (e.g., lipid solubility)
 3 main – bioavailability of drug
 Cmax: point of max conc. In plasma.
◦ Expressed in mcg/ml
◦ Dependent on
 Dose administered
 Rate of absorption
 Rate of elemination
 Tmax: time taken to attain Cmax
 Expressed in hrs
 Onset of action is depended on tmax
 AUC: total integrated area under plasma level-time and
expresses the amount of drug that reaches the systemic
circulation
 Routes of Drug Administration
◦ Oral (per os, p.o.)
◦ Inhalation
 vapors, gases, smoke
◦ Mucous membranes
 intranasal (sniffing)
 sublingual
 rectal suppositories
◦ Injection (parenteral)
 intravenous (IV)
 intramuscular (IM)
 subcutaneous (SC)
 intraperitoneal (IP; nonhumans only)
◦ Transdermal
 The process by which drug proceeds from the site of
administration to the site of measurement (blood stream)
within the body.
 Necessary for the production of a therapeutic effect.
 Most drugs undergo gastrointestinal absorption. This is extent
to which drug is absorbed from gut lumen into portal
circulation
 Exception: IV drug administration
 The movement of drug from the blood
to and from the tissues
 Determined by:
 • partitioning across various membranes
 •binding to tissue components
 •binding to blood components (RBC, plasma protein)
 •physiological volumes
Introduction to pharmacokinetics
Introduction to pharmacokinetics
Introduction to pharmacokinetics

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Introduction to pharmacokinetics

  • 2.  The study of the disposition of a drug  The disposition of a drug includes the processes of ADME  Absorption  Distribution  Metabolism  Excretion  Drug concentration at sites of action influenced by several factors, such as: ◦ Route of administration ◦ Dose ◦ Characteristics of drug molecules (e.g., lipid solubility)
  • 3.
  • 4.  3 main – bioavailability of drug  Cmax: point of max conc. In plasma. ◦ Expressed in mcg/ml ◦ Dependent on  Dose administered  Rate of absorption  Rate of elemination  Tmax: time taken to attain Cmax  Expressed in hrs  Onset of action is depended on tmax  AUC: total integrated area under plasma level-time and expresses the amount of drug that reaches the systemic circulation
  • 5.
  • 6.  Routes of Drug Administration ◦ Oral (per os, p.o.) ◦ Inhalation  vapors, gases, smoke ◦ Mucous membranes  intranasal (sniffing)  sublingual  rectal suppositories ◦ Injection (parenteral)  intravenous (IV)  intramuscular (IM)  subcutaneous (SC)  intraperitoneal (IP; nonhumans only) ◦ Transdermal
  • 7.  The process by which drug proceeds from the site of administration to the site of measurement (blood stream) within the body.  Necessary for the production of a therapeutic effect.  Most drugs undergo gastrointestinal absorption. This is extent to which drug is absorbed from gut lumen into portal circulation  Exception: IV drug administration
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.  The movement of drug from the blood to and from the tissues  Determined by:  • partitioning across various membranes  •binding to tissue components  •binding to blood components (RBC, plasma protein)  •physiological volumes