Km is
inversely related to the affinity
Vmax is
Directly proportional to enzyme concentration
Increase y-intercept on Lineweaver-Burk plot means
Decrease in Vmax
Competitive inhibiotrs do what on a Lineweaver-Burk plot
Bring Km closer to 0
No change to Vmax (y-intercept)
Bioavailability (F)=
AUCo / AUCIV
Volume of distribution (Vd) =
Dose / [P]
Drug with low Vd found in
Blood
Drug with medium Vd found in
ECF
Drug with High Vd found in
All tissues
t1/2=
[0.7 X Vd] / Cl
Cl=
Rate of elimination / [P]
Vd X K
Loading dose=
[Cp x Vd] / F
Maintenance dose=
[Cp x Cl x τ] / F
Zero PEAs for me
Drugs with zero order of elimination
Phase 1 drug metabolism
Phase 2 drug metabolism
Efficacy is
Maximal effect a drug can produce
Potency is
Amount of drug needed for a given effect
α1 major functions
α2 major function
Hemicholinium action
Inhibits Choline uptake
Vesamicol action
Inhibits ACh storage
Botulinum action
Inhibit ACh release
Metyrosine action
Inhibit formation of DOPA from Tyrosine