Naturally occurring oleic and undecylenic acids were used as raw materials for the synthesis of novel polyurethanes (PUs). The application of environmentally friendly thiol‐ene additions to 10‐undecenoate and oleate derivatives was studied with the goal of obtaining renewable diols. The resulting monomers were then polymerized with 4,4′‐methylenebis (phenylisocyanate), in N,N‐dimethylformamide solution using tin (II) 2‐ethylhexanoate as catalyst, to produce the corresponding thermoplastic PUs (TPUs). Also, ultrasound irradiation has been tested to improve the synthesis of PU. Under these conditions, TPUs were obtained in high yields (80–99%) with weight‐average molecular weights in the 36–83 kDa range. The chemical structures of PUs were assessed by FTIR and NMR spectroscopy. The thermal and mechanical properties of the synthesized TPUs have been studied and they showed a clear dependence on the structure of the parent diol. MTT test was carried out to asses the potential cytotoxicity of the prepared PUs, indicating no cytotoxic response. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011

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For tissue engineering purpose biopolymer chondroitin sulfate (CS), one of the major components of cartilage and bone extracellular matrix, was immobilized onto the surface of amino-functionalized polyurethane (PU) films derived from naturally occurring oleic and 10-undecenoic acids. The amino-functionalized PUs were prepared by aminolysis with 1,6-hexamethylenediamine of synthesized PUs containing methyl ester groups. FTIR-ATR, XPS, SEM, and water contact angle measurements were used to confirm the surface changes at each step of treatment, both in morphologies and chemical composition. Cytotoxicity and cell morphology analysis using osteoblast cell line MG63 showed that PU-CS films are suitable materials for cell growth, spreading, and differentiation.