Mathematical Kinetic Modeling on Isoniazid Release from Dex-HEMA-PNIPAAm Nanogels

Abstract

<br /><strong>Objective(s)</strong><strong>:</strong> The quantitative calculation of release data is more facil when mathematics come to help. mathematically modeling could aid optimizing and amending the delivery systems design. Aim of this study is to find out the isoniazid release kinetic. <br /><strong>Methods:</strong> In this work degradable temperature sensitive dextran-hydroxy ethyl methacrylate- poly-N-isopropyl acryl amide (Dex-HEMA-PNIPAAm) nanogels which were synthesized by UV polymerization were loaded by Isoniazid. The Isoniazid release amounts taken from in vitro studies at two different temperatures, below and upper lower criticalsolution temperature (LCST) were mathematically modeled to investigate the kinetic of drug release. Mathematically inquiry of release phenomenon of Isoniazid makes it easy to predict and recognize the influence of delivery device laying out parameters on release kinetic formulation. The modeling was performed using model dependent methods, such as zero order, first order, Higuchi, Korsmeyer- Pepas, Hixon and Crowel. <br /><strong>Results: </strong>The best fitted model showing the highest determination coefficient (R2) was Korsmeyer-Pepas which means predominant release mechanism is controlled by diffusion. <br /><strong>Conclusions:</strong> The Isoniazid release pattern of most samples was combination of swelling, diffusion and degradation.