Pharmacokinetics Ch 11 Flashcards
Pharmacodynamics
Study of how drugs interact with their targets.
Pharmocokinetics (acronym?)
Study of drug reaches its target and how it is affected along the way. Absorption Distribution Metabolism Excretion
Oral drug absorption (3)
Need to survive acidic conditions of stomach and digestive enzymes.
Need to absorbed by intestinal lining and pass through pores into blood stream (polar enough to dissolve in blood but hydrophobic enough to pass through cell membrane).
Processed by liver.
Lipinkski’s Rule of 5
MW<+5
Henderson Hasselbalch equation
pH=pKa+log[A-]/[HA]
logP
logP= log([solute]oct/[solute]water)
logD
logD=log(([A-]oct/[HA]oct)/([A-]wat/[HA]wat))
Oral Absorption of Polar drugs (3)
Small enough to pass between cells.
Recognized by carrier proteins.
Carried across by pinocytosis.
Drug distribution
Speed? What can slow it down?
Distribution is rapid once drug is in blood stream.
Binding to plasma proteins slows because capillary cells have pores that do not let proteins cross.
Blood brain barrier
Capillaries do not contain pores and are coated with fatty layer so polar drugs cannot cross.
Phase I Drug Metabolism (3)
Oxidation by Cytochorome P450 enzymes.
Oxidation by Flavin Monooxygenases.
Transformation by other enzymes.
Cyochrome P450 Enzymes
33 Heme containing monooygenases in 4 families. Use NADPH and O2.
Phase II Drug Metabolism (3)
Conjugation reactions
Methylation
Acetylation
Glucuronidation
Glucuronyltransferase adds glucuronate from UDFP glucuronate to phenol, alcohol, or carboxylic acids.
Sulfoconjugations
Sulfotransferases add to phenols, alcohols, and amines.