TABLE 1.
Kinetics parameters of protein released from microparticles for 28 days.
Model | Equation | Parameters | HSA-alone | IL-4 N1 | IL-4 N2 | HSA N1 | HSA N2 |
---|---|---|---|---|---|---|---|
Zero order | Q = K0t + Q0 | K0 | 0.787 | 0.005 | 0.004 | 0.474 | 0.341 |
Q0 | 14.417 | 0.102 | 0.237 | 19.452 | 26.381 | ||
R2 | 0.969 | 0.627 | 0.418 | 0.741 | 0.729 | ||
First order | Q = 1 – e −K 1 t | K1 | 0.237 | 0.574 | 0.794 | 0.825 | 0.963 |
R2 | 0.649 | 0.992 | 0.971 | 0.837 | 0.717 | ||
Higuchi | Q = KHt1/2 | KH | 7.175 | 0.052 | 0.082 | 7.700 | 8.649 |
R2 | 0.751 | 0.229 | −2.605 | −1.678 | −6.468 | ||
Ritger-Peppas | Q = Ktn | K | 11.689 | 0.096 | 0.210 | 17.741 | 23.930 |
R2 | 0.957 | 0.877 | 0.754 | 0.950 | 0.941 |
Q is the cumulative amount of drug released at time t; K0, K1, KH, and K are regarded as kinetic constant for zero-order release, first-order release, Higuchi, and Ritger-Peppas, respectively. And n is the diffusional exponent denoting the drug transport mechanism.