Pharmacology Flashcards
Half-life
Time taken for the concentration of a drug to decrease by half
Volume of distribution
The apparent volume a drug disperses into at steady state to produce the observed concentration
Clearance
Amount of plasma cleared of drug per unit time. The units are the same as flow, in L/min
Hepatic clearance
Volume of blood cleared of drug, by the liver, per unit time.
First-order kinetics
Rate of reaction is dependent on the concentration of reactant, mostly used in the concept of elimination, when a constant % of drug is eliminated per unit time
Zero-order process
Rate of reaction is independent of the concentration of reactant. Constant amount of drug eliminated per unit time
Bioavailability
The % of drug reaching the systemic circulation, expressed as a fraction of the same amount of drug given IV
What is hepatic extraction ratio
Fraction of substance removed from blood flowing through the liver during a single pass.
Context-sensitive half time
Time taken for the plasma concentration to fall by 50% after the cessation of drug infusion, with the context being the duration of infusion
Ke0
Rate constant of drug elimination from the effect site.
Main determinant of the time to peak effect from a bolus of drug.
T1/2 Ke0
Value which describes the time taken to achieve 50% effect-site concentration when the plasma levels are maintained at steady state
Purpose of TCI?
Achieve and maintain a predetermined target concentration of said drug, rapidly, and without overshooting
Bristol method
Achieve plasma [propofol] of 3 microg/ml
Loading 1mg/kg
Immediate infusion at 10mg/kg/hr for 10 mins
then 8mg/kg/hr for 10 mins
then 6mg/kg/hr for 10mins
Plus N2O
Typical remifentanil infusion targets?
plasma target
4ng/ml, or 0.2ug/kg/min infusion
Drug
Any compound that affects a biochemical or physiological effect in the body
mechanisms of drug effects
Physicochemical: mannitol, chelating agents
Receptor interaction
Enzyme activity alteration