Liver and Metabolism 14 Pharmacokinetics 1 – Drug absorption Flashcards
what are the 6 rights of prescribing
Right patient Right drug Right route Right dose Right time Right outcome
what is pharmacokinetics
what the body does to the drug
what is pharmacodynamics
what the drug does to the body
therapeutic effect
what does pharmacokinetics do
Facilitates safe and effective use of medicines
Determines optimal dosage regimen (dose, route, dose interval, duration of treatment)
Predicts potential drug interactions
what makes up pharmacokinetics
absorption - Drug transfer from its site of
administration to the systemic circulation (blood)
distribution
metabolism
excretion
Factors that influence enteral absorption
Gastrointestinal (GI) motility Absorptive area GI blood flow Drug particle size and formulation Drug physicochemical properties Drug binding
routes of drug administration
oral
rectal
(sublingual
buccal)
how does solubility effect enteral absorption
lipid soluble - non polarised eg NaCl
hydrophilic (polar) - ionised molecules (Na, K)
more lipid soluble - more absorption, more water soluble, less absorption
how does pH affect absorption
acidic drugs better absorbed by acidic media (same for basic)
acidic better absorbed by stomach and basic by intestines
better excreted in opposite media (important for poisoning)
routes of drug administration
parenteral (injection) Topical Transdermal Inhalational Intrathecal
what is ideal dosing
between minimum toxic concentration and minimum effective concentration
pharmacokinetic concepts
Absorption First-pass (pre-systemic metabolism) Bioavailability Bioequivalence Volume of distribution Cytochrome P450 enzyme system Half-life Steady state Clearance
what is bioavailability
Fraction of the administered (oral) dose of a drug that reaches the systemic circulation.
20% OBA needs to be 5x IV dose
Oral AUC/IV AUC
what is first pass (pre-systemic) metabolism
metabolism of the drug prior to reaching systemic circulation.
hepatic
smaller it is, the greater the BA
what is bioequivalence
Two drugs are considered bioequivalent when there is no significant difference in the rate or extent of bioavailability at the same molar dose and under the same conditions
relevant for different formulas and batches