Table 4: Kinetic profiles of in vitro drug release from different selected microemulsions through dialysis membrane.

Batch code Zero order First order Higuchi Koresmeyer-Peppas Hixon-Crowell
Dt = D0 + k0 t ln Dt = ln D0 + k1 t Dt = D0 + kH t1/2 Dt/D = KKP tn Dt1/3 = D0 1/3 - KHC t
R2 K0 R2 K1 R2 KH R2 n* KKP R2 KHC
OAVM-2 0.9384 0.1045 0.9680 -0.0012 0.9937 3.2447 0.9892 0.4898 0.5257 0.9908 -0.0027
IPMVM-8 0.9601 0.1070 0.9111 -0.0013 0.9710 3.3987 0.9588 0.5124 0.4288 0.9546 -0.0024
IPMVM-11 0.9417 0.1036 0.9364 -0.00011 0.9749 3.1935 0.9660 0.4693 0.3870 0.9711 -0.0026
IPPVM-14 0.9640 0.0991 0.9623 -0.0015 0.9876 3.2148 0.9862 0.5604 0.2854 0.9843 -0.0026
IPPVM-15 0.9438 0.0971 0.9360 -0.0014 0.9819 3.3981 0.9588 0.5189 0.4329 0.9710 -0.0027
IPPVM-17 0.9280 0.0947 0.9508 -0.0008 0.9841 2.8742 0.9801 0.4833 0.5074 0.9773 -0.0025

Where,
Dt is the amount of drug released at time t, D0 is the initial amount of drug released, Dt/D is fraction of drug released at time t, k0 is the zero order release constant, k1 is the first order release constant, kH is the Higuchi release constant, kHC is the Hixson-Crowell rate constant, KKP is the Koresmeyer-Peppas release constant, R2 is the regression coefficient values of drug release data calculated from various drug release kinetic models, n* is the diffusional exponent.