Direct ink writing of vancomycin‐loaded polycaprolactone/ polyethylene oxide/ hydroxyapatite 3D scaffolds

• DOI: 10.1111/jace.18048
• Publication Date: 2021-07-21T18:02:14Z
• Authors: Bin Zhang; Alexander K. Nguyen; Roger J. Narayan; Jie Huang
• Keywords: bone tissue scaffold; hydroxyapatite; 02 engineering and technology; 551; mechanical property; printing; bioceramics; processing; ink rheology behavior; 0210 nano-technology; direct ink writing; drug release

AbstractNovel inks were formulated by dissolving polycaprolactone (PCL), a hydrophobic polymer, in organic solvent systems; polyethylene oxide (PEO) was incorporated to extend the range of hydrophilicity of the system. Hydroxyapatite (HAp) with a weight ratio of 55–85% was added to the polymer‐based solution to mimic the material composition of natural bone tissue. The direct ink writing (DIW) technique was applied to extrude the formulated inks to fabricate the predesigned tissue scaffold structures; the influence of HAp concentration was investigated. The results indicate that in comparison to other inks containing HAp (55%, 75%, and 85%w/w), the ink containing 65% w/w HAp had faster ink recovery behavior; the fabricated scaffold had a rougher surface as well as better mechanical properties and wettability. It is noted that the 65% w/w HAp concentration is similar to the inorganic composition of natural bone tissue. The elastic modulus values of PCL/PEO/HAp scaffolds were in the range of 4–12 MPa; the values were dependent on the HAp concentration. Furthermore, vancomycin as a model drug was successfully encapsulated in the PCL/PEO/HAp composite scaffold for drug release applications. This paper presents novel drug‐loaded PCL/PEO/HAp inks for 3D scaffold fabrication using the DIW printing technique for potential bone scaffold applications.