Term
|
Definition
Value of [substrate] which equals 1/2 of Vmax
Determines the enzyme affinity toward substrate: Smaller Km (small substrate) means HIGHER affinity because only a small substrate concentration needed to achieve 1/2Vmax
Larger Km (large substrate) means LOWER affinity because it takes a large amount of substrate to achieve 1/2Vmax |
|
|
Term
|
Definition
The speed of the reaction at which all the enzymes are occupied with substrate (supersaturated). |
|
|
Term
|
Definition
Vd (volume drug was dissolved in) = Amount of drug /Plasma concentration of drug
Rearranged from simply: Plasma concentration of drug = Amount of drug/Volume that drug was dissolved in |
|
|
Term
|
Definition
CL = (0.7 x Vd)/T-halflife
Rearranged to find halflife: T-halflife = (0.7 x Vd)/CL |
|
|
Term
|
Definition
Loading dose = Cp (target concentration)/ Vd |
|
|
Term
|
Definition
Maintenance Dose = Cp(target concentration)/CL
Replace what was lost (Clearance amount) |
|
|
Term
Competitive Inhibitor effects on Km and Vmax |
|
Definition
Km increases (needs more substrate to overcome the inhibitor)
Vmax remains unchanged (inhibitor did not do anything to effect the quality of the enzyme) |
|
|
Term
Non-Competitive (irreversible) inhibitor effects on Km and Vmax |
|
Definition
Km remains the same
Vmax Decreases (allosteric binding of inhibitor causes conformational change of enzyme. Quality of reaction is effected) |
|
|
Term
|
Definition
Lethal Dose 50/Therapeutic Dose50
The larger the therapeutic index, the safer the drug is. (higher LD50 and lower TD50) |
|
|