Oxygen and ionic transport in hydrogel and silicone-hydrogel contact lens materials: An experimental and theoretical study

Handle

https://riunet.upv.es/handle/10251/51422

Cita bibliográfica

Pozuelo, J.; Compañ Moreno, V.; González Méijome, J.; González, M.; Mollá Romano, S. (2014). Oxygen and ionic transport in hydrogel and silicone-hydrogel contact lens materials: An experimental and theoretical study. Journal of Membrane Science. 452:62-72. https://doi.org/10.1016/j.memsci.2013.10.010

Titulación

Resumen

[EN] 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 siloxane phase. The values of diffusion coefficient of O2, water and Na+ and Cl− ions in Si-Hy 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 wt% 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 found experimentally for Na+ diffusion coefficients are between three or five times lower than MDS. For Si-Hy materials with 36 wt% of water the Na+ permeability, diffusion coefficient and salt partition coefficient (km=P/D) are 6.7±0.2×10−7 cm2/s, 1.8±0.5×10−6 cm2/s and 0.42±0.13, respectively. For Hy materials of 38.6 wt% the values found were 18.4±1.2×10−7 cm2/s, 5.4±1.0×10−6 cm2/s and 0.34±0.09, respectively. The coordination number between the fixed groups (single bondSiOsingle bond) and water in HEMA and the particles (O2, 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.

Fuente

Journal of Membrane Science issn: 0376-7388

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