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!Dose | !Dose | ||
|Amount of active drug given to patient | |Amount of active drug given to patient | ||
|mg (D) | |align="center"|mg (D) | ||
|Drug Specific (From clinical studies) | |Drug Specific (From clinical studies) | ||
|- | |- | ||
!Concentration | !Concentration | ||
|Amount of drug in a given plasma volume | |Amount of drug in a given plasma volume | ||
|µg/ml (C) | |align="center"|µg/ml (C) | ||
|= D / Vd | |align="center"|= D / Vd | ||
|- | |- | ||
!EC<sub>50</sub> | !EC<sub>50</sub> | ||
|The concentration of drug needed to elicit a response halfway between zero and maximal responses. | |The concentration of drug needed to elicit a response halfway between zero and maximal responses. | ||
|µg/ml (EC<sub>50</sub>) | |align="center"|µg/ml (EC<sub>50</sub>) | ||
|align="center"|y = bottom + (Top-Bottom)/(1+ [x/EC50] Hill Coefficient) | |align="center"|y = bottom + (Top-Bottom)/(1+ [x/EC50] Hill Coefficient) | ||
|- | |- | ||
!Volume of Distribution | !Volume of Distribution | ||
|The theoretical volume the drug would occupy if distributed uniformly throughout the tissues to elicit the current plasma concentration. | |The theoretical volume the drug would occupy if distributed uniformly throughout the tissues to elicit the current plasma concentration. | ||
|L (Vd) | |align="center"|L (Vd) | ||
|D / C | |align="center"|D / C | ||
|- | |- | ||
!Elimination Constant (Rate) | !Elimination Constant (Rate) | ||
|The rate at which the drug is removed from the body. | |The rate at which the drug is removed from the body. | ||
|h-1 (Ke) | |align="center"|h-1 (Ke) | ||
|ln(2) / t1/2 or CL / Vd | |align="center"|ln(2) / t1/2 or CL / Vd | ||
|- | |- | ||
!Bioavailability | !Bioavailability | ||
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!Cmax or Cmin | !Cmax or Cmin | ||
|The maximum (Cmax) / minimum (Cmin) plasma drug concentration reached following drug administration | |The maximum (Cmax) / minimum (Cmin) plasma drug concentration reached following drug administration | ||
|µg/ml (Cmax or Cmin) | |align="center"|µg/ml (Cmax or Cmin) | ||
|Identified via direct measurement of plasma C | |Identified via direct measurement of plasma C | ||
|- | |- | ||
!tmax | !tmax | ||
|The time it takes for a drug to reach Cmax following administration | |The time it takes for a drug to reach Cmax following administration | ||
|h (tmax) | |align="center"|h (tmax) | ||
|Identified via direct measurement of plasma C over time | |Identified via direct measurement of plasma C over time | ||
|- | |- | ||
!Half-life | !Half-life | ||
|The time it takes for a drug to reach half its original concentration | |The time it takes for a drug to reach half its original concentration | ||
|h (t1/2) | |align="center"|h (t1/2) | ||
|ln(2) / Ke | |align="center"|ln(2) / Ke | ||
|- | |- | ||
!Drug Clearance | !Drug Clearance | ||
|The volume of plasma cleared of the drug over a set time | |The volume of plasma cleared of the drug over a set time | ||
|l/h (CL) | |align="center"|l/h (CL) | ||
|Vd x Ke or D / Area under curve | |align="center"|Vd x Ke or D / Area under curve | ||
|} | |} | ||
edits