The transport of oxygen, water and naked ions of Na+ and Cl- across two kind of hydrogels materials, made of a conventional hydrogel (Hy) based on hydroxyethyl methacrylate (pHEMA) and a silicone hydrogel (Si Hy) material containing siloxane moieties, was compared between Molecular Dynamics Simulations (MDS) and experimental measurements. Computer assisted simulations were carried out for wet hydrogels at 310 K and equilibrium water uptake in the range from 10% to 40%. Our results show that in Si Hy materials the aqueous hydrogel and hydrophobic siloxane phases are separated suggesting a co -continuous structure, and oxygen moves predominantly through the free volume of the hydrophobic siffixanc phase. The values of diffusion coefficient of O-2, water and Na+ and Cl- ions in Si Fly was about one order of magnitude higher than in conventional hydrogels when the water content was above 25 wt % up to a critical value of 35 wL% where a percolation phenomenon is observed. The value of the oxygen diffusion coefficient obtained by simulations are roughly similar to that experimentally found using potentiostatic techniques. Values founcl experimentally for Na+ diffusion coefficients are between three or five Limes lower than MDS. For Si Fly materials with 36 wt% of water the Na+ permeability, diffusion coefficient and salt partition coefficient (k(m)=P/D) are 6.7 +/- 0.2 x 10(-7) cm(2)/s, 1.8 +/- 0.5 x 10(-6) cm(2)/s and 0.42 +/- 0.13, respectively. For Fly materials of 38.6 wt% the values found were 18.4 +/- 1.2 x 10(-7) cm(2)/s, 5.4 +/- 1.0 x 10(-6) cm(2)/s and 0.34 +/- 0.09, respectively. The coordination number between the fixed groups (-SiO-) and water in HEMA and the particles (O-2, Cl- and Na+) is slightly larger than unity. The present study might be applied in the modeling of the gas transport in hydrogels as well as in novel polymeric structures for novel polymeric structures for new biomedical and technological applications with the aim of predicting and tuning their physiological behavior. (C) 2013 Elsevier B.V. All rights reserved.