Compact Saloplastic Poly(Acrylic Acid)/Poly(Allylamine) Complexes: Kinetic Control Over Composition,Microstructure, and Mechanical Properties |
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Authors: | Andreas Reisch Patricia Tirado Emilie Roger Fouzia Boulmedais Dominique Collin Jean‐Claude Voegel Benoît Frisch Pierre Schaaf Joseph B. Schlenoff |
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Affiliation: | 1. Laboratoire de Conception et Application, de Molécules Bioactives, UMR 7199, CNRS/Université de Strasbourg, Faculté de Pharmacie, 74 route du Rhin, 67401 Illkirch Cedex, France, and International Center for Frontier, Research in Chemistry, 8 allée Gaspard Monge, 67083 Strasbourg, France;2. Centre National de la Recherche Scientifique, Institut Charles Sadron, UPR 22, 23 rue du Loess, 67034 Strasbourg Cedex, France, and International Center for Frontier Research in Chemistry, 8 allée Gaspard Monge, 67083 Strasbourg, France.;3. Institut National de la Santé et de la Recherche Médicale, INSERM Unité 977, 11 rue Humann, 67085 Strasbourg Cedex, France.;4. Department of Chemistry and Biochemistry, The Florida State University, Tallahassee, FL 32306, USA |
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Abstract: | Durable compact polyelectrolyte complexes (CoPECs) with controlled porosity and mechanical properties are prepared by ultracentrifugation. Because the starting materials, poly(allylamine hydrochloride) (PAH) and poly(acrylic acid sodium salt) (PAA), are weak acids/bases, both composition and morphology are controlled by solution pH. In addition, the nonequilibrium nature of polyelectrolyte complexation can be exploited to provide a range of compositions and porosities under the influence of polyelectrolyte addition order and speed, and concentration. Confocal microscopy shows these “saloplastic” materials to be highly porous, where pore formation is attributed to a combination of deswelling of the polyelectrolyte matrix and expansion of small inhomogenities by osmotic pressure. The porosity (15–70%) and the pore size (<5 μm to >70 μm) of these materials can be tuned by adjusting the PAA to PAH ratio, the salt concentration, and the pH. The modulus of these CoPECs depends on the ratio of the two polyelectrolytes, with stoichiometric complexes being the stiffest due to optimized charge pairing, which correlates with maximized crosslinking density. Mechanical properties, pore sizes, and pore density of these materials make them well suited to three dimensional supports for tissue engineering applications. |
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Keywords: | hydrogels polymeric materials porous materials stimuli‐responsive materials tissue engineering |
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