Abstract

In this article, a method to develop 3D printable hybrid sodium alginate and albumin foam, crosslinked with calcium chloride mist is introduced. Using this method, highly porous structures are produced without the need of further postprocessing (such as freeze drying). The proposed method is particularly beneficial in the development of wound dressing as the printed foams show excellent lift-off and water absorption properties. Compared with methods that use liquid crosslinker, the use of mist prevents the leaching of biocompounds into the liquid crosslinker. 3D printing technique was chosen to provide more versatility over the wound dressing geometry. Calcium chloride and rhodamine B were used as the crosslinking material and the model drug, respectively. Various biomaterial inks were prepared by different concentrations of sodium alginate and albumin, and the fabricated scaffolds were crosslinked in mist, liquid, or kept without crosslinking. The effects of biomaterial composition and the crosslinking density on the wound dressing properties were assessed through printability studies. The mist-crosslinked biomaterial ink composed of 1% (w/v) sodium alginate and 12% (w/v) albumin showed the superior printability. The fabricated scaffolds were also characterized through porosity, mechanical, degradation, and drug release tests. The mist-crosslinked scaffolds showed superior mechanical properties and provided relatively prolonged drug release.

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