how to calculate bioavailability
area under curve for IV drugs
IV route has what bioavailablity
when is the bioavailability of drugs measured
acidic drugs bind what
basic drugs bind what
hydrophobic drugs bind what
steroid hormones bind what
what part of the drug can be cleared renally?
if you have a high volume of distribution, where does the drug go?
- more in the interstitial and intracellular fluid
if you have a low volume of distribution, where does the drug go?
how to calculate volume of distribution
Vd = Q/Cp
Q= amount of drug in body Cp= plasma drug concentration
Clearance and plasma concentration of a drug with high Vd
- low plasma concentration
clearance and plasma concentration of a drug with low Vd
- high plasma concentration
how to calculate renal clearance
CL = UV/P
U= drug concentration in urine V = flow rate P = plasma concentration of drug
half life of drug formula considering CL
t1/2 = (0.7*Vd)/CL
half life of a drug as Vd increases
half life of a drug as CL increases
calculation of elimination rate constant (Ke)
Ke = CL/Vd
half life concentration in regard to Ke
t1/2=0.7/Ke
what does a higher elimination constant mean
how to calculate maintenance dose
MD = (CpCLт)/F
т=dosage interval
F=bioavailability
Cp=plasma concentration at steady state
how to calculate loading dose
LD = (Cp*Vd)/F
F = bioavailability
Cp=plasma concentration at steady state
what is loading dose