Cmin
Cmin is a term used in pharmacokinetics for the minimum blood plasma concentration reached by a drug during a dosing interval, which is the time interval between administration of two doses. This definition is slightly different from Ctrough, the concentration immediately prior to administration of the next dose.[1] Cmin is the opposite of Cmax, the maximum concentration that the drug reaches. Cmin must be above certain thresholds, such as the minimum inhibitory concentration (MIC), to achieve a therapeutic effect.[2]
In most cases Cmin is directly measurable. At steady state the minimum plasma concentration can also be calculated using the following equation:[3]
- S = Salt factor
- F = Bioavailability
- D = Dose
- ke = Elimination rate constant
- ka = Absorption rate constant
- Vd = Volume of distribution
- τ = Dosing interval
Cmin is also an important parameter in bioavailability and bioequivalence studies, it is part of the pharmacokinetic information recommended for submission of investigational new drug applications.[4]
References
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- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value). [bare URL PDF]
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