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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 3.

Some of the functions describing the relationship between in vivo and in vitro drug dissolution.

Description Function
Identity F22, t) = F11, t)
Linear F22, t) = θ51 + θ52F11, t)
Sigmoid F2(θ2,t)=θ51+θ52F1(θ1,t)θ53θ54+F1(θ1,t)θ53
Higuchi F22, t) = (θ51F11, t))0.5
Hixon-Crowell F2(θ2,t)=θ51(θ510.33θ52F1(θ1,t))3
Weibull F22, t) = θ51 − θ52e(−θ53(F11,t))θ54

θ5i (i = 1, 2, 3, 4): parameter θ5 (see equation 10) at observation times t1, t2, t3, t4.