Abstract
Organic–inorganic xerogel networks were synthesized from bacterial poly (3-hydroxybutyrate) (PHB) for potential biomedical applications. Since silane-based networks usually demonstrate increased biocompatibility and mechanical properties, siloxane groups have been added onto polyurethane (PU) architectures. In this work, a diol oligomer (oligoPHB-diol) was first prepared from bacterial poly(3-hydroxybutyrate) (PHB) with an environmentally friendly method. Then, hexamethylene diisocyanate or biobased dimeryl diisocyanate was used as diisocyanate to react with the short oligoPHB-diol for the synthesis of different NCO-terminated PU systems in a bulk process and without catalyst. Various PU systems containing increasing NCO/OH molar ratios were prepared. Siloxane precursors were then obtained after reaction of the NCO-terminated PUs with (3-aminopropyl)triethoxysilane, resulting in silane-terminated polymers. These structures were confirmed by different analytical techniques. Finally, four series of xerogels were prepared via a sol–gel process from the siloxane precursors, and their properties were evaluated depending on varying parameters such as the inorganic network crosslinking density. The final xerogels exhibited adequate properties in connection with biomedical applications such as a high in vitro degradation up to 15 wt% after 12 weeks.
Highlights
Nicolas Sbirrazzuoli, AndreiaPolyurethanes (PUs) are one of the main polymer families, with a ranking of 6th amongst all polymers [1] due to their wide range of applications, easy synthesis and great possibility to adapt their properties by varying their formulation
Several additional physico-chemical and thermal properties were given in a previous publication [32]
The chemical structure of the four PU prepolymer (PUP) was confirmed by 1 H-NMR
Summary
Nicolas Sbirrazzuoli, AndreiaPolyurethanes (PUs) are one of the main polymer families, with a ranking of 6th amongst all polymers [1] due to their wide range of applications, easy synthesis and great possibility to adapt their properties by varying their formulation. White biotechnology, which is a branch of biotechnology using living organisms for the synthesis of new molecules and macromolecules, is largely developed to obtain different building blocks (short molecules), macromers, or bacterial biopolymers such as Polyhydroxyalkanoates (PHA), a family of biopolyesters [6,14]. From these molecules and macromolecules, new architectures can be synthesized and tailored for specific applications
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