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In the context of controlled release drug delivery approaches, the systems providing zero-order release kinetics have special advantages. Through employing these systems, drug concentration could be maintained within the therapeutic window over release time; thus maximum effectiveness alongside minimized side effects of the drug are achieved. However, obtaining zero-order drug release is extremely challenging. One of the main obstacles is the fact that implemented devices should be designed to overcome the decreasing mass transfer driving force, especially, in polymeric systems in which diffusion mechanism is dominant. In this study, we developed a new configuration of a polymeric matrix... 

Numerical and analytical exact solutions of diffusional release from a cylindrical polymeric matrix into an infinite medium have been developed in which the initial solute loading (A) is greater than solubility limit (Cs). Also, the effects of boundary layers on the drug release rate have been studied. The numerical solution is valid for any initial drug loading whereas analytical solution can be used for high values of drug loading. Comparisons have been made between numerical and analytical exact solutions in upper and lower bounds (A/Cs蠑1 and A/Cs→1) and previously presented approximate solution. The presented results validate the proposed numerical solution  

The biofluids being manipulated in lab-on-a-chip devices usually contain elastic macromolecules. Accordingly, for an accurate modeling of the relevant flow physics one should invoke viscoelastic constitutive equations. In this paper, attention is paid toward the hydrodynamic dispersion by the fully developed electroosmotic flow of PTT viscoelastic fluids in slit microchannels of low zeta potential. Adopting the Taylor–Aris approach, analytical solutions are derived for late-time solute concentration and effective dispersion coefficient. Finite element-based numerical simulations are also conducted to monitor the broadening of an analyte band from the moment of injection. Both approaches are...