Lecture 1 Flashcards
What is PK
Pharmacokinetics. What the body does to the drug.. the fate of the molecule. ADME
What is PD
Pharmacodynamics. What the drug does to the body… the biological effect/ Efficacy
What is the A in ADME
Absorption. the passage of a drug from its site of administration into the systemic circulation
What is the D is ADME
Distribution. the movement of drug from site of absorption to site of action and the site of metabolism or excretion
What is the M is ADME
Metabolism. Irreversible alteration of drug chemistry
What is the E is ADME
Excretion. Passage of drug or metabolites out of the body
Examples of excretion in ADME
Renal and Biliary pathways
Examples of Metabolism in ADME
Hepatic, oxidation, reduction, and conjugation
examples of distribution in ADME
Perfusion, permeability, and binding
examples of absorption is ADME
dosage form, site, chemical and biological interactions
High drug concentrations is toxic or subtherapeutic?
Toxic
Low drug concentrations are toxic or subtherapeutic
sub therapeutic
How is whole blood obtained
Venous punction, contains and anticoagulant such as heparin or EDTA
How is Serum Obtained
WHole blood is allowed to clot and the clot is removed
How is plasma obtained
Centrifugation of nonclotted whole blood that contains an anticoagulant
Components of whole blood
All the cellular and protein elements of blood
Components of Serum
Does not contain cellular elements, fibrinogen or the other clotting factors
Components of plasma
Noncellular liquid fraction of the whole blood, contains all the proteins and clotting factors
What is AUC, and what does it find
The area under the Curve describes the exposure of drugs to the body
What is MTC
Minimum toxic concentration, a Concentration that you have to be careful to not go above
What is MEC
Minimum effective concentration. A concentration that you have to reach so you can see therapeutic effect
What is a therapeutic window
The useful range of concentration over which a drug is therapeutically beneficial
How should you change dosing for a drug with narrow therapeutic windows
Smaller and more frequent doses. A different method of administration
How should you change dosing for a drug with a slow elimination rate
One large initial dose, followed by smaller doses