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. Author manuscript; available in PMC: 2012 Oct 10.
Published in final edited form as: Int J Pharm. 2011 Jan 13;418(1):142–148. doi: 10.1016/j.ijpharm.2011.01.010

Table 1.

Some of the functions used to describe the unit impulse function.

Parameters One compartment Two compartments
  • V: apparent volume of distribution

  • ke: first order elimination rate constant

  • ka: first order absorption rate constant

  • k12: rate constant for transfer from central to peripheral compartment

  • k21: rate constant for transfer from peripheral to central compartment

  • ·

    Single compartment = body

  • ·

    Even distribution of drug throughout body

  • ·

    Only applicable for rapidly distributed drug

  • ·

    Central compartment (drug in and out) + peripheral compartment (drug distribution)

  • ·

    Slow equilibration between compartments

Without absorption
  • ·

    Very rapidly absorbed drug (almost ideal)

r(t)=1Ve(ket) r(t)=kaV(kake)[e(ket)e(kat)]
With absorption
  • ·

    Commonly applicable

  • ·

    Severely influenced by physicochemical, biopharmaceutical, and physiological factors

r(t)=kaV[k21ka(λ1ka)(λ2ka)e(kat)+k21λ1(kaλ1)(λ2λ1)e(λ1t)+k21λ2(kaλ2)(λ1λ2)e(λ2t)] r(t)=AVe(λ1t)+1AVe(λ2t)

λ12 = ke+ k12+ k21; λ1 λ2 = ke k21; A = (k21 − λ1)/(λ2 − λ1).